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articles

  • Recent advances in transition-metal-catalyzed asymmetric reactions of diazo compounds with electron-rich (hetero-) arenes.  59:2307-2316. 2018
  • Development of a scalable synthetic route towards a 2,2,6-trisubstituted chiral morpholine via stereoselective hydroalkoxylation.  59:1808-1812. 2018
  • Tricine as a convenient scaffold for the synthesis of C-terminally branched collagen-model peptides.  59:130-134. 2018
  • Synthesis of novel HIV-1 protease inhibitors via diastereoselective Henry reaction with nitrocyclopropane.  58:1123-1126. 2017
  • Palladium catalyzed C-H functionalization with electrochemical oxidation.  58:797-802. 2017
  • Improved and expanded one-pot, two-component Boulton-Katritzky syntheses of N-N bond containing bicyclic heterocycles.  58:202-205. 2017
  • Multigram-scale synthesis of enantiopure 3,3-difluoroproline.  57:5658-5660. 2016
  • Copper-catalyzed C-N cross-coupling of arylboronic acids with N-acylpyrazoles.  57:3604-3607. 2016
  • Total synthesis of calothrixins and their analogues via formal 3+2 cycloaddition of arynes and 2-aminophenanthridinedione.  57:3481-3484. 2016
  • Synthesis of 2-aryl-2H-tetrazoles via a regioselective [3+2] cycloaddition reaction.  57:1597-1599. 2016
  • Cavitands with inwardly and outwardly directed functional groups.  56:4824-4828. 2015
  • A Zincke aldehyde approach to gelsemine.  56:3165-3168. 2015
  • A divergent/convergent approach to dolabriferol: the Kornblum-DeLaMare enantiomeric resolution.  56:3643-3646. 2015
  • A five-membered lactone prodrug of CBI-based analogs of the duocarmycins.  56:3101-3104. 2015
  • Enantio- and diastereoselective synthesis of syn-β-hydroxy-α-alkenyl carboxamides via reductive aldol reactions of morpholine 4-methyl-2,3-pentadienoic carboxamide with diisopinocampheylborane.  56:3281-3284. 2015
  • Enantioselective synthesis of tertiary α-chloro esters by non-covalent catalysis.  56:3428-3430. 2015
  • Isomerization of coencapsulated molecules.  56:3117-3119. 2015
  • Solid-phase synthesis of peptides containing bulky dehydroamino acids.  56:3311-3313. 2015
  • Studies in selective 6-membered bromoether formation via bromonium and thiiranium-induced cyclizations.  56:3553-3556. 2015
  • Synthesis of triarylmethanols via tandem arylation/oxiddation of diarylmethanes.  56:3604-3607. 2015
  • Total synthesis of clavosolide A via tandem allylic oxidation/oxa-conjugate addition reaction.  56:3120-3122. 2015
  • Preparation of tetrasubstituted pyrimido 4,5-d pyrimidine diones.  56:1949-1952. 2015
  • A metal-free and recyclable synthesis of benzothiazoles using thiourea as a sulfur surrogate.  56:1709-1712. 2015
  • A synthesis of abemaciclib utilizing a Leuckart-Wallach reaction.  56:949-951. 2015
  • A chemoenzymatic approach toward the preparation of site-specific antibody-drug conjugates.  56:3172-3175. 2015
  • Tandem cyclization reactions of electron rich arylethylamino acid amides. An entry to the dihydroimidazoisoquinolin-3(2H)-one ring system.  55:4837-4839. 2014
  • Lewis acid facilitated regioselective synthesis of tau-histidinoalanine.  55:3114-3116. 2014
  • Hexanes/acetonitrile: a binary solvent system for the efficient monosilylation of symmetric primary and secondary diols.  55:2600-2602. 2014
  • Synthesis of densely functionalized α-methylene γ-butyrolactones via an organocatalytic one-pot allylic-alkylation–cyclization reaction.  55:479-482. 2014
  • Diethylaminosulfur trifluoride-mediated intramolecular cyclization of 2-hydroxycycloalkylureas to fused bicyclic aminooxazoline compounds and evaluation of their biochemical activity against beta-secretase-1 (BACE-1).  54:5802-5807. 2013
  • Efficient microwave-assisted solid phase coupling of nucleosides, small library generation, and mild conditions for release of nucleoside derivatives.  54:1869-1872. 2013
  • Effect of acid catalysis on the direct electrophilic fluorination of ketones, ketals, and enamides using selectfluor (tm).  53:2971-2975. 2012
  • A cleavable scaffold strategy for the synthesis of one-bead one-compound cyclic peptoid libraries that can be sequenced by tandem mass spectrometry.  53:2341-2344. 2012
  • Synthesis of 4-azepanones and heteroaromatic-fused azepines.  53:723-725. 2012
  • Enantioselective concomitant creation of vicinal quaternary stereogenic centers via cyclization of alkynols triggered addition of azlactones.  52:5963-5967. 2011
  • Expanding the scope of the Cu assisted Suzuki-Miyaura reaction.  52:5055-5059. 2011
  • Intramolecular Michael reactions of aliphatic aldehyde enolates generated by imidazolium carbenes.  52:2468-2470. 2011
  • A Diels-Alder reaction conducted within the parameters of aqueous organocatalysis: Still just smoke and mirrors.  52:2085-2087. 2011
  • Generation of quaternary centers by reductive cross-coupling: Shifting of regioselectivity in a subset of allylic alcohol-based coupling reactions.  52:2144-2147. 2011
  • Programmable one-pot synthesis of tumor-associated carbohydrate antigens lewis x dimer and kh-1 epitopes.  52:2132-2135. 2011
  • Reactivity of N-nitrosoamides in confined spaces.  52:2100-2103. 2011
  • Stereoselective synthesis of the decahydrofluorene core of the hirsutellones.  52:2072-2075. 2011
  • Total synthesis and biological evaluation of marinopyrrole A and analogues.  52:2041-2043. 2011
  • Concise, efficient and practical assembly of bromo-5,6-dimethoxyindole building blocks.  52:1339-1342. 2011
  • Novel two-step, one-pot synthesis of primary acylureas.  51:5843-5844. 2010
  • Synthesis of 1,5-disubstituted tetrazoles via Suzuki-Miyaura cross-coupling of 5-chloro-1-phenyltetrazole.  51:3473-3476. 2010
  • Synthesis of farinomalein.  51:1710-1712. 2010
  • Efficient and library-friendly synthesis of furo- and thieno 2,3-d pyrimidin-4-amine derivatives by microwave irradiation.  51:629-632. 2010
  • Synthesis of labeled meropenem for the analysis of M. tuberculosis transpeptidases.  51:197-200. 2010
  • Microwave-assisted stereoselective alpha-2-deoxyglycosylation of hex-1-en-3-uloses.  50:7327-7329. 2009
  • A tryptophan-analog host whose interactions with ammonium ions in water are dominated by the hydrophobic effect.  50:7035-7037. 2009
  • Synthesis of 10 stereochemically distinct bis-tetrahydrofuran intermediates for creating a library of 64 asimicin stereoisomers.  50:6398-6401. 2009
  • Synthesis of novel aryl-1,2-oxazoles from ortho-hydroxyaryloximes.  50:6173-6175. 2009
  • Evaluation of chlorofusin, its seven chromophore diastereomers, and key analogues.  50:3151-3153. 2009
  • Studies toward the duocarmycin prodrugs for the antibody prodrug therapy approach.  50:2932-2935. 2009
  • Novel and efficient synthesis of 4-sulfonyl-2-pyridones.  50:2094-2096. 2009
  • Total synthesis of tovophyllin b.  50:1161-1163. 2009
  • N-tosylimidates in highly enantioselective organocatalytic michael reactions.  50:145-147. 2009
  • Decarboxylation and ring fragmentation reactions of sydnone N-oxides.  49:4550-4552. 2008
  • An improved synthesis of haloacetamidine-based inactivators of protein arginine deiminase 4 (pad4).  49:4383-4385. 2008
  • Convenient synthesis of 1,1 '-H-spiro[indoline-3,3 '-piperidine].  49:4372-4373. 2008
  • Suzuki-Miyaura cross-coupling of alpha-phosphoryloxy enol ethers with arylboronic acids.  49:4142-4144. 2008
  • Controlled derivatization of polyhalogenated quinolines utilizing selective cross-coupling reactions.  49:3137-3141. 2008
  • Optimized 'inverse activation' methodology for esterification of hydroxyl-functionalized resins.  49:2907-2910. 2008
  • Synthesis of pyridazines functionalized with amino acid side chains.  49:903-905. 2008
  • Iron(III) p-toluenesulfonate catalyzed synthesis of homoallyl ethers from acetals and aldehydes.  48:8665-8667. 2007
  • Synthesis of brasilibactin A and confirmation of absolute configuration of β-hydroxy acid fragment.  48:8104-8107. 2007
  • Synthesis of fluorinated 1,8-naphthyridinone derivatives.  48:8189-8191. 2007
  • Synthesis of monofluorinated 1-(naphthalen-1-yl)piperazines.  48:5539-5541. 2007
  • The Cu-I-catalyzed exo-selective asymmetric multicomponent C+NC+CC coupling reaction.  48:3867-3870. 2007
  • Synthesis of chromanyl and dihydrobenzofuranyl piperazines.  48:3039-3041. 2007
  • Novel Cinchona alkaloid derived ammonium salts as catalysts for the asymmetric synthesis of β-hydroxy α-amino acids via aldol reactions.  48:2083-2086. 2007
  • Amine-catalyzed michael reactions of an aminoaldehyde derivative to nitroolefins.  48:693-696. 2007
  • Novel route to the synthesis of 4-quinolyl isothiocyanates.  47:2161-2164. 2006
  • Regioselective aldol condensations of a cholestanone-derived dialdehyde: new twists on a classic reaction.  47:2083-2086. 2006
  • Highly efficient synthesis of sialylglycopeptides overcoming unexpected aspartimide formation during activation of Fmoc-Asn(undecadisialyloligosaccharide)-OH.  47:1341-1346. 2006
  • High-yielding macrocyclization conditions used in the synthesis of novel Sansalvamide A derivatives.  47:515-517. 2006
  • Symmetrical biodegradable crosslinkers for use in polymeric devices.  46:8921-8925. 2005
  • Environment friendly organic synthesis using bismuth compounds. An efficient method for carbonyl-ene reactions catalyzed by bismuth triflate.  46:7747-7750. 2005
  • Solid-phase synthesis of oxazolones and other heterocycles via wang resin-bound diazocarbonyls.  46:5495-5498. 2005
  • Different reaction routes found in acid-catalyzed glycosylation of endo- and exo-glycals: competition between Ferrier rearrangement and protonation.  46:5071-5076. 2005
  • Kinetic resolution by copper-catalyzed azide-alkyne cycloaddition.  46:4543-4546. 2005
  • Asymmetric dihydroxylation catalyzed by ionic polymer-supported osmium tetroxide.  46:4491-4493. 2005
  • Total synthesis of didmolamides A and B.  46:2567-2570. 2005
  • A thermally-cleavable linker for solid-phase synthesis.  46:1181-1184. 2005
  • Novel method for catalyst immobilization using an ionic polymer: A case study using recyclable ytterbium triflate.  46:807-810. 2005
  • Diastereo- and enantio-selective crotylation of alpha-ketoesters using crotyl boronic acid ester complexes.  45:8285-8288. 2004
  • In situ cyclopropanation: a rapid one-pot method for the synthesis of resin bound cyclopropyl phenyl methanones as combinatorial scaffolds.  45:7331-7334. 2004
  • Solid-phase synthesis of 3,4-dihydro-1H-pyrimidine-2-ones using sodium benzenesulfinate as a traceless linker.  45:6545-6547. 2004
  • Amino alcohol catalyzed direct asymmetric aldol reactions: Enantioselective synthesis of anti-alpha-fluoro-beta-hydroxy ketones.  45:5681-5684. 2004
  • General microwave-assisted protocols for the expedient synthesis of quinoxalines and heterocyclic pyrazines.  45:4873-4876. 2004
  • Aminoglycoside array for the high-throughput analysis of small molecule-rna interactions.  45:3639-3642. 2004
  • Assembly of sugars on polystyrene plates: A new facile microarray fabrication technique.  45:2689-2692. 2004
  • Sequential aldol condensation catalyzed by dera mutant ser238asp and a formal total synthesis of atorvastatin.  45:2439-2441. 2004
  • Rapid access to epothilone analogs via semisynthetic degradation and reconstruction of epothilone D.  45:1945-1947. 2004
  • CBr4-photoirradiation protocol for chemoselective deprotection of acid labile primary hydroxyl protecting groups.  45:635-639. 2004
  • Rapid analysis of solvent effects on enamine formation by fluorescence: How might enzymes facilitate enamine chemistry with primary amines?.  45:325-328. 2004
  • Smart cleavage reactions: The synthesis of benzimidazoles and benzothiazoles from polymer-bound esters.  45:313-316. 2004
  • A search for dichlorocarbene ether solvent interactions.  45:485-486. 2004
  • Rucl3-promoted amide formation from azides and thioacids.  44:9083-9085. 2003
  • Thermodynamic equilibration of dihydropyridone enolates: application to the total synthesis of (+/-)-epiuleine.  44:9185-9188. 2003
  • A concise stereospecific synthesis of repinotan (BAYx3702).  44:8563-8565. 2003
  • Near-IR absorption of porphyrin methylcarbocations.  44:7753-7756. 2003
  • Studies on novel macrocyclization methods of cembrane-type diterpenoids: a Stille cyclization approach to (+/-)-isocembrene.  44:5921-5923. 2003
  • A concise route to phytosphingosine from lyxose.  44:5281-5283. 2003
  • Access to the noryohimban [6,5,6,5,6] ring system via an intramolecular furan Diels-Alder reaction.  44:5137-5140. 2003
  • Novel construction of the brassinolide side chain.  44:5107-5108. 2003
  • Synthesis of the (S,S,S)-diastereomer of the 15-membered biaryl ring system of RP 66453.  44:4019-4022. 2003
  • Direct organocatalytic asymmetric mannich-type reactions in aqueous media: One-pot mannich-allylation reactions.  44:1923-1926. 2003
  • Proline-catalyzed asymmetric assembly reactions: Enzyme-like assembly of carbohydrates and polyketides from three aldehyde substrates.  43:9591-9595. 2002
  • Solid phase synthesis of 3,5-disubstituted oxazolidin-2-ones.  43:8327-8330. 2002
  • A convenient and highly stereoselective approach for alpha-galactosylation performed by galactopyranosyl dibenzyl phosphite with remote participating groups.  43:7721-7723. 2002
  • Anti-selective smp-catalyzed direct asymmetric mannich-type reactions: Synthesis of functionalized amino acid derivatives.  43:7749-7752. 2002
  • Amine-catalyzed direct self diels-alder reactions of alpha,beta-unsaturated ketones in water: Synthesis of pro-chiral cyclohexanones.  43:6743-6746. 2002
  • Inter- and intramolecular alcohol additions to exo-glycals.  43:6515-6519. 2002
  • Synthesis and evaluation of six-membered GDP-iminocyclitol.  43:5691-5693. 2002
  • The preparation of polymer bound beta-ketoesters and their conversion into an array of oxazoles.  43:5407-5410. 2002
  • Synthesis of the C(18)-(C26) segment of superstolide A.  43:4885-4887. 2002
  • An efficient method for the cleavage of p-methoxybenzylidene (PMP), tetrahydropyranyl (THP) and 1,3-dithiane protecting groups by Selectfluor™.  43:4037-4039. 2002
  • Amine-catalyzed direct diels-alder reactions of alpha,beta-unsaturated ketones with nitro olefins.  43:3817-3820. 2002
  • Selectfluor ™-mediated allylstannation of aldehydes and imines.  43:3915-3917. 2002
  • An efficient method for the preparation of 2-hydroxy- and 2-aminoglycals from glycosyl sulfoxides.  43:3447-3448. 2002
  • A novel approach to amidines from esters.  43:419-421. 2002
  • Preparation of the 14-membered L,L-cycloisodityrosine subunit of RP 66453.  43:407-410. 2002
  • Solid phase peptide synthesis on JandaJel(TM) resin.  43:37-40. 2002
  • Expanding the diversity of purine libraries.  42:8751-8755. 2001
  • Enantioselective approach to 3-substituted prolines.  42:8571-8573. 2001
  • Use of a racemic derivatizing agent for measurement of enantiomeric excess by circular dichroism spectroscopy.  42:8015-8018. 2001
  • A novel diterpenoid lactone-based scaffold for the generation of combinatorial libraries.  42:7119-7121. 2001
  • Facile synthesis of conjugated exo-glycals.  42:6907-6910. 2001
  • A new facile method for the stereoselective synthesis of trans-2-aryl-3,3-dimethylcyclopropane-1-carboxylic acids.  42:6227-6229. 2001
  • Alternative synthesis and thermal atropisomerism of a fully functionalized DEFG ring system of teicoplanin.  42:6061-6064. 2001
  • Expeditious synthesis of C-glycosyl conjugated dienes and aldehydes from sugar lactones.  42:4657-4660. 2001
  • Catalytic enantioselective direct michael additions of ketones to alkylidene malonates.  42:4441-4444. 2001
  • Convenient synthesis of 2-deoxy-scyllo-inosose and 2-deoxy-scyllo-inosamine: Two key intermediates on the biosynthetic pathway to aminoglycoside antibiotics.  42:4219-4221. 2001
  • Sequential removal of the benzyl-type protecting groups pmb and nap by oxidative cleavage using can and ddq.  42:4033-4036. 2001
  • Synthesis of oxazolidinyl azacycles via ring-closing olefin metathesis: a practical entry to the synthesis of deoxy-azasugars and hydroxypyrrolizidines.  42:4079-4082. 2001
  • An unusual regioselectivity in the Pd-catalyzed cross coupling of alkynes. A correction.  42:3775-3778. 2001
  • Measurement of enantiomeric excess of amines by mass spectrometry following kinetic resolution with solid-phase chiral acylating agents.  42:2617-2619. 2001
  • A novel method for the synthesis of aryl sulfones.  42:2281-2283. 2001
  • Glycosyl trifluoroacetimidates. Part 1: Preparation and application as new glycosyl donors.  42:2405-2407. 2001
  • Rearrangement of methylenecamphor during electrophilic bromination: remarkably clean access to the unnatural fenchyl (1,3,3-trimethylbicyclo[2.2.1]heptane) system.  42:2261-2263. 2001
  • Solid-phase synthesis of oligoesters using a JandaJel (tm) resin.  42:2257-2259. 2001
  • Synthesis of N-acetylglucosamine thiazoline/lipid II hybrids.  42:615-618. 2001
  • Amine-catalyzed direct asymmetric mannich-type reactions.  42:199-201. 2001
  • (E)-gamma-(dimethylphenylsilyl)allyl diisopinocampheylborane: a highly enantioselective reagent for the synthesis of anti-beta-hydroxyallylsilanes.  41:9413-9417. 2000
  • An amino acid that controls polypeptide helicity: beta-amino alanine, the first strongly stabilizing C-terminal helix stop signal.  41:9679-9683. 2000
  • Deep cavitands for anion recognition.  41:9547-9551. 2000
  • Design and synthesis of cyclic sialyl lewis x mimetics: A remarkable enhancement of inhibition by pre-organizing all essential functional groups.  41:9499-9503. 2000
  • Synthesis and evaluation of a novel bleomycin A(2) analogue: Continuing assessment of the linker domain.  41:9493-9498. 2000
  • Improved synthesis of (4-ethenylphenyl)diphenyl methanol and its application in the preparation of trityl functionalized polystyrene resin containing tetrahydrofuran derived cross-linker.  41:8417-8420. 2000
  • Regioselective synthesis of fluoroaldols. Studies toward fluoroepothilones syntheses via antibody catalysis.  41:8243-8246. 2000
  • Efficient synthesis of triazoles from d-arabinose and l-fucose.  41:7805-7808. 2000
  • A proline-catalyzed asymmetric robinson annulation reaction.  41:6951-6954. 2000
  • Deprotection of n-tert-butoxycarbonyl (boc) groups in the presence of tert-butyl esters.  41:7013-7016. 2000
  • Ring-closing olefin metathesis of prearranged C-allyl saccharides for the synthesis of C-butenyl linked homo- and hetero-disaccharides.  41:6593-6597. 2000
  • Solid-phase combinatorial synthesis of 5-arylalkylidene rhodanine.  41:5729-5732. 2000
  • Synthesis of a second-generation pseudopeptide platform.  41:5013-5016. 2000
  • A self-assembled phthalocyanine dimer.  41:3777-3780. 2000
  • The expeditious preparation and reactivity of some protected forms of gluconolactones.  41:2569-2572. 2000
  • Enantioselective synthesis of protected forms of (3R,5R)-5-hydroxypiperazic acid useful for synthesis.  41:289-292. 2000
  • Direct conversion of benzyl alcohol to ketone by polymer-supported Rh catalyst.  40:8897-8900. 1999
  • Catalytic single-chain antibodies possessing beta-lactamase activity selected from a phage displayed combinatorial library using a mechanism-based inhibitor.  40:8063-8066. 1999
  • Tpm: A new protecting group for alkynes.  40:7861-7865. 1999
  • Phosphorodithioates: Synthesis and evaluation of new haptens for the generation of antibody acyl transferases.  40:7307-7310. 1999
  • Formation of the 1,2,6-orthoester of mannose and its utilization in the glycosylation reaction.  40:6423-6426. 1999
  • New supports for solid-phase organic synthesis: Development of polystyrene resins containing tetrahydrofuran derived cross-linkers.  40:6329-6332. 1999
  • The osmium-catalyzed aminohydroxylation of baylis-hillman olefins.  40:5151-5154. 1999
  • Studies of fragment assembly aldol reactions of chiral aldehydes and chiral methyl ketones: stereoselective synthesis of the C(13)-C(25) segment of scytophycin C.  40:4955-4959. 1999
  • Stereochemically divergent pathways for the allylation and crotylation reactions of anti- and syn-beta-hydroxy-alpha-methyl aldehydes with allyl- and crotyltrifluorosilanes.  40:4643-4647. 1999
  • Comparison of amine additives most effective in the new methyltrioxorhenium-catalyzed epoxidation process.  40:3991-3994. 1999
  • A pseudopeptide platform with side chains addressable for combinatorial applications.  40:3511-3514. 1999
  • A triphenylene scaffold with c-3v-symmetry and nanoscale dimensions.  40:3515-3518. 1999
  • Towards the synthesis of spongistatin 1: diastereoselective synthesis of the C(36)-C(45) subunit.  40:3351-3354. 1999
  • Solid-phase synthesis of potential aspartic acid protease inhibitors containing a hydroxyethylamine isostere.  40:2729-2732. 1999
  • Preferential hydrogenolysis of nap esters provides a new orthogonal protecting group strategy for carboxylic acids.  40:1803-1806. 1999
  • A short enantioselective synthesis of 1-deoxy-l-xylulose by antibody catalysis.  40:1437-1440. 1999
  • An improved synthesis of the (E,Z)-dienoate precursor of (+)-damavaricin D via a vinylogous Horner-Wadsworth-Emmons reaction.  40:1269-1272. 1999
  • Synthesis of fluorinated olefins via the palladium catalyzed cross-coupling reaction of 1-fluorovinyl halides with organoboranes.  40:827-830. 1999
  • A convenient oxidative deprotection of tetrahydropyranyl ethers with iron(iii) nitrate and clay under microwave irradiation in solvent free conditions.  40:561-562. 1999
  • Palladium-catalyzed coupling of functionalized bromoarenes to a polystyrene-bound aryl tributylstannane.  40:415-418. 1999
  • Synthesis of dendrimers containing 2,5-anhydro-D-mannitol as a chiral, tetrafunctional central core with C-2 symmetry.  39:9161-9164. 1998
  • An efficient synthesis of tetrasubstituted imidazoles from N-(2-oxo)-amides.  39:8939-8942. 1998
  • Expanding on the purification methodology of polyethylene glycol (PEG) bound molecules: The synthesis of 3,5-pyrazolidinediones.  39:8433-8436. 1998
  • A convenient one-pot synthesis of 4-amino-3-arylpyrazoles from alpha-phthaloylaminoacetophenones.  39:8229-8232. 1998
  • Catalytic aminohydroxylation using adenine-derivatives as the nitrogen source.  39:7669-7672. 1998
  • Solid-phase combinatorial synthesis of 4-hydroxyquinolin-2(1H)-ones.  39:6399-6402. 1998
  • Natural products analogs as scaffolds for supramolecular and combinatorial chemistry.  39:5709-5712. 1998
  • Total synthesis of naturally occurring prostaglandin F2 alpha on a non-cross-linked polystyrene support.  39:3943-3946. 1998
  • N-chloro-n-sodio-2-trimethylsilyl ethyl carbamate: A new nitrogen source for the catalytic asymmetric aminohydroxylation.  39:3667-3670. 1998
  • Reversal of regioselection in the asymmetric aminohydroxylation of cinnamates.  39:2507-2510. 1998
  • Synthesis of CC-1065 and duocarmycin analogs via intramolecular aryl radical cyclization of a tethered vinyl chloride.  39:2227-2230. 1998
  • Unexpected 1,3-oxazolidine formation in the attempted oxidation of N-aryl-N-methyl substituted beta-amino alcohols using pyridinium dichromate.  39:2269-2272. 1998
  • Solid-phase C-acylation of active methylene compounds.  39:2195-2198. 1998
  • Bifunctional initiators for free radical polymerization of non-crosslinked block copolymers.  39:1513-1516. 1998
  • A concise route to isocanthin-6-one.  39:1111-1112. 1998
  • A simple and efficient method for the preparation of pyridine-n-oxides ii.  39:761-764. 1998
  • An intramolecular Diels-Alder approach to the spirotetronic acid subunits of the quartromicins.  38:8781-8784. 1997
  • Second generation synthesis of the quartromicin spirotetronic acid subunits via a Claisen rearrangement intramolecular aldol sequence.  38:8785-8788. 1997
  • Synthesis and photophysics of a novel porphyrin-c-60 hybrid.  38:8133-8136. 1997
  • The effect of lithium bromide and lithium chloride on the reactivity of SmI2 in THF.  38:8157-8158. 1997
  • Synthesis of diverse ethoxyformacetal oligomers. Toward libraries of metal-coordinating unnatural biopolymers.  38:7825-7828. 1997
  • Palladium/copper (I) halide-cocatalyzed stereospecific coupling of 1-fluorovinylstannanes with aryl iodides and acyl chlorides.  38:7677-7680. 1997
  • One-pot synthesis of 1-allyl- and 1-allenyl-6-O-acetyl-2,3,4-tri-O-benzyl-α-D-glycosides from methyl tetra-O-benzyl-α-D-glycosides.  38:5419-5422. 1997
  • Syntheses of alkylated malonates on a traceless linker derived soluble polymer support.  38:5437-5440. 1997
  • Preparation and inverse electron demand diels-alder reactions of 3-methoxy-6-methylthio-1,2,4,5-tetrazine.  38:3805-3808. 1997
  • Synthetic studies on maduropeptin chromophore .2. Synthesis of the madurosamine aryl amide and the c1'-c9' fragments.  38:3671-3674. 1997
  • Synthesis of a versatile purification handle for use with Boc chemistry solid phase peptide synthesis.  38:3361-3364. 1997
  • Sialic acid aldolase-catalyzed condensation of pyruvate and N-substituted mannosamine: A useful method for the synthesis of N-substituted sialic acids.  38:2649-2652. 1997
  • A soluble polymer-bound approach to the sharpless catalytic asymmetric dihydroxylation (AD) reaction: Preparation and application of a (DHQD)(2)PHAL-PEG-OMe ligand.  38:1527-1530. 1997
  • Combinatorial synthesis of 2,9-substituted purines.  38:1161-1164. 1997
  • Soluble polymer synthesis: An improved traceless linker methodology for aliphatic C-H bond formation.  38:977-980. 1997
  • Diastereofacially selective enolate Claisen rearrangements of 4-7-eta 4-(1-acyloxy-2,4,6-octatrienyl) tricarbonyliron complexes.  38:351-354. 1997
  • Synthetic studies on maduropeptin chromophore .1. Construction of the aryl ether and attempted synthesis of the 7.3.0 bicyclic system.  38:3667-3670. 1997
  • Synthesis of the melanoma-associated ganglioside 9-O-acetyl GD3 through regioselective enzymatic acetylation of GD3 using subtilisin.  37:9271-9274. 1996
  • C-fucopeptides as selectin antagonists: Attachment of lipid moieties enhances the activity.  37:9033-9036. 1996
  • C-mannose derivatives as potent mimics of sialyl lewis x.  37:9037-9040. 1996
  • Diastereoselective synthesis of the cis-octahydronaphthalene nucleus of superstolides A and B.  37:8989-8992. 1996
  • Long-range asymmetric induction by conjugate addition to alkenylcyclohexadienyliron complexes.  37:9009-9012. 1996
  • Diastereoselective synthesis of the trans-anti-cis-decahydro-as-indacene ring system via the transannular Diels-Alder reaction of a functionalized (E,E,E)-cyclododeca-1,6,8-triene.  37:8065-8068. 1996
  • A linker that allows efficient formation of aliphatic C-H bonds on polymeric supports.  37:6491-6494. 1996
  • Enzymatic resolution of amines and amino alcohols using pent-4-enoyl derivatives.  37:6287-6290. 1996
  • Metal catalyzed diazo transfer for the synthesis of azides from amines.  37:6029-6032. 1996
  • The solid phase synthesis of N-alkylcarbamate oligomers.  37:5653-5656. 1996
  • Design and synthesis of a cocaine-diamide hapten for vaccine development.  37:5479-5482. 1996
  • Synthesis of sialyl Lewis X mimetics: Use of O-α-fucosyl-(1R, 2R)-2-aminocyclohexanol as core structure.  37:5427-5430. 1996
  • Synthesis of a cyclic urea as a nonnatural biopolymer scaffold.  37:5309-5312. 1996
  • The solid phase synthesis of oligoureas.  37:5305-5308. 1996
  • Synthesis of glycosyl chlorides with acid-labile protecting groups.  37:4903-4906. 1996
  • A practical route to enantiopure 1,2-aminoalcohols.  37:3219-3222. 1996
  • Kinetic and thermodynamic control of l-threonine aldolase catalyzed reaction and its application to the synthesis of mycestericin d.  37:2791-2794. 1996
  • An asymmetric synthesis of (+)-isonitramine by 'triple allylic strain-controlled' intramolecular S(N)2' alkylation.  37:1433-1434. 1996
  • Modular approach to annonaceous acetogenins. Total synthesis of asimicin and bullatacin.  36:9257-9260. 1995
  • Synthesis of vicinal diamines from cyclic sulfates.  36:9241-9244. 1995
  • Synthesis and solid state structure of an unsymmetrical triurea.  36:8535-8538. 1995
  • Synthesis and inhibition analysis of 5-membered homoazasugars from d-arabinofuranose via an sn2 reaction of the chloromethylsulfonate.  36:8247-8250. 1995
  • Synthesis of a cyclitol via a tandem enzymatic aldol - intramolecular horner-wadsworth-emmons reaction.  36:7057-7060. 1995
  • Asymmetric dihydroxylation affords enantiomerically pure c-12 building-blocks from trans,trans,cis-1,5,9-cyclododecatriene.  36:6603-6606. 1995
  • An efficient chemoenzymatic synthesis of alpha-amino-beta-hydroxy-gamma-butyrolactone.  36:5063-5064. 1995
  • L-threonine aldolase in organic-synthesis - preparation of novel beta-hydroxy-alpha-amino acids.  36:4081-4084. 1995
  • Diastereoselective aldol reactions of chiral aldehydes and chiral methyl ketones: dependence of stereoselectivity on the metal enolate, the aldehyde 2,3-stereochemistry, and the aldehyde β-alkoxy protecting group.  36:3443-3446. 1995
  • Synthesis of the C(3)-C(15) segment of rutamycin B via a C(8)-C(9) fragment assembly aldol reaction: metal dependence of the aldehyde and enolate diastereofacial selectivities.  36:3447-3450. 1995
  • Enzymatic resolution of a key stereochemical intermediate for the synthesis of (-)-taxol.  36:3291-3294. 1995
  • A short, efficient chiral synthesis of a novel cholinergic channel activator, ABT-418 (S)-3-methyl-5-(1-methyl-2-pyrrolidinyl)isoxazole, from (S)-pyroglutamic acid.  36:2563-2566. 1995
  • Barrelene derivatives: potential modules for assembly.  36:1813-1816. 1995
  • Carbonucleotoids and carbopeptoids - new carbohydrate oligomers.  36:1775-1778. 1995
  • Diastereoselective synthesis of N-benzoyl mycalamine, the fully elaborated trioxadecalin nucleus of mycalamide. A. Control of the key N-acyl aminal stereocenter via carbamate acylation.  36:1581-1584. 1995
  • Preparation of a neoglycolipid carrying the oligosaccharide component of saponin from albizzia julibrissin.  36:1509-1510. 1995
  • Asymmetric synthesis of two-residue modules designed for mimicry of beta strands.  36:691-694. 1995
  • Diisopropyl tartrate-modified (E)-γ-[(menthofuryl)dimethylsilyl]-allyl boronate, an improved chiral reagent for the anti α-hydroxyallylation of aldehydes. Application to the enantioselective synthesis of (−)-swainsonine.  36:501-504. 1995
  • Cyclobutylcarbinyl radical cleavage in the bicyclo[3.2.0]heptanone ring-system.  36:459-460. 1995
  • A novel case of cationic rearrangement involving a phenonium ion.  35:8295-8298. 1994
  • Photochemical analog of the bergman cycloaromatization reaction.  35:8089-8092. 1994
  • Synthesis of iminothiasugar as a potential transition-state analog inhibitor of glycosyltransfer reactions.  35:8243-8246. 1994
  • Comparing 2 models for the selectivity in the asymmetric dihydroxylation reaction (ad).  35:7315-7318. 1994
  • Highly stereoselective 1,4-addition reactions of alkylidene malonate substituted η4-(1,3-butadienyl)iron(tricarbonyl) complexes.  35:7351-7354. 1994
  • Highly stereoselective substitution reactions of functionalized η4-[3(E),5(E)-heptadien-2-ol]iron tricarbonyl complexes.  35:7347-7350. 1994
  • New synthetic receptors derived from porphyrins.  35:6823-6826. 1994
  • Synthesis of alpha,alpha-dialkylated amino acids with adenine or thymine residues a new mild and facile hydrolysis of hydantoins.  35:6635-6638. 1994
  • Diastereoselectivity in cyclopropanation and epoxidation reactions of chiral (E)-crotylsilanes: asymmetric synthesis of substituted tetrahydrofurans.  35:6453-6456. 1994
  • An efficient synthesis of enantiomerically pure trans-2-phenylcyclohexanol.  35:5611-5612. 1994
  • Synthesis and rotational properties of a series of polyaromatic clefts.  35:5359-5362. 1994
  • A facile synthesis of 1-thiopentofuranoside.  35:5257-5260. 1994
  • Asymmetric dihydroxylation of olefins containing sulfur - chemoselective oxidation of c-c double-bonds in the presence of sulfides, 1,3-dithianes, and disulfides.  35:5129-5132. 1994
  • A stereochemically general synthesis of methyl 2,4,6-trideoxy-4-methylthio-α-D-ribo-pyranoside, the thio sugar of esperamicin A(1).  35:4931-4934. 1994
  • Asymmetric synthesis of the hydroxylamino sugar of calicheamicin.  35:4935-4938. 1994
  • Synthesis and stereochemical assignments for goniobutenolide-a and goniobutenolide-b.  35:4685-4688. 1994
  • An enantioselective approach to the synthesis of manzamine-a.  35:4279-4282. 1994
  • Microchemical structural determination of a peptoid covalently bound to a polymeric bead by matrix-assisted laser-desorption ionization time-of-flight mass-spectrometry.  35:4283-4286. 1994
  • Catalysis of carbamate hydrolysis by an antibody.  35:3873-3876. 1994
  • Asymmetric dihydroxylation of primary allylic halides and a concise synthesis of (-)-diepoxybutane.  35:3469-3472. 1994
  • Divergent mechanisms for the dealkoxycarbonylation of a 2-(3-azetidinyl)malonate by chloride and cyanide.  35:3441-3444. 1994
  • Synthesis of a guanidino-sugar as a glycosyl cation mimic.  35:3481-3484. 1994
  • A new 5+1 route to arenes - application to the facile synthesis of d-4-symmetrical chiral porphyrins.  35:2465-2468. 1994
  • Study of the regioselectivity and enantioselectivity of the reactions of osmium-tetroxide with allylic alcohols and allylic sulfonamides.  35:2495-2498. 1994
  • Formation of the oxatricyclo[3.2.1.0(3,6)]octane ring-system via an intramolecular bromoetherification.  35:2221-2222. 1994
  • Molecular recognition of adenine: role of geometry, electronic effects and rotational restrictions.  35:1035-1038. 1994
  • Conformationally constrained amino-acids - synthesis of novel 3,4-cyclized tryptophans.  35:939-940. 1994
  • The asymmetric dihydroxylation of cis-allylic and homoallylic alcohols.  35:843-846. 1994
  • Comparison of ligands proposed for the asymmetric dihydroxylation.  35:543-546. 1994
  • Chemoenzymatic synthesis of homoazasugars.  35:359-362. 1994
  • An expedient synthesis of isopropyl anisoles and veratroles.  35:4509-4510. 1994
  • Concerning the diastereofacial selectivity of aldol reactions of chiral methyl ketone enolates: evidence for remote chelation in the bafilomycin aldol reaction.  34:8387-8390. 1993
  • Asymmetric dihydroxylation of tertiary allylic alcohols.  34:8225-8228. 1993
  • Bis(tri-n-butylstannyl)benzopinacolate - preparation and use as a mediator of intermolecular free-radical reactions.  34:7819-7822. 1993
  • Facile esterification of sulfonic acids and carboxylic acids with triethylorthoacetate.  34:7355-7358. 1993
  • Modified cinchona alkaloid ligands - improved selectivities in the osmium-tetroxide catalyzed asymmetric dihydroxylation (ad) of terminal olefins.  34:7375-7378. 1993
  • Multipoint recognition of carboxylates by neutral hosts in nonpolar solvents.  34:6837-6840. 1993
  • Synthesis of naphthyl A–B disaccharides corresponding to olivomycin A and mithramycin.  34:6829-6832. 1993
  • Asymmetric dihydroxylation (ad)/cyclization of n-diboc allylic and homoallylic amines - selective differentiation of the hydroxyl-groups.  34:5545-5548. 1993
  • Double diastereoselection in asymmetric dihydroxylation.  34:5575-5578. 1993
  • Lithium bis(2-adamantyl)amide - structure and reactivity of an extremely hindered lithium dialkylamide.  34:5213-5216. 1993
  • Synthesis and transannular diels-alder reactions of (E,E,E)-cyclotetradeca-2,8,10-trienones.  34:4427-4430. 1993
  • A new multienzyme system for a one-pot synthesis of sialyl oligosaccharides - combined use of beta-galactosidase and alpha(2,6)-sialyltransferase coupled with regeneration insitu of cmp-sialic acid.  34:3091-3094. 1993
  • Synthesis of optically-active secondary allylic alcohols from allylsilanes via successive asymmetric dihydroxylation (ad) and peterson olefination reactions.  34:2509-2512. 1993
  • Asymmetric dihydroxylation of aryl allyl ethers.  34:2267-2270. 1993
  • Asymmetric dihydroxylation (ad) of n,n-dialkyl and n-methoxy-n-methyl alpha,beta-unsaturated and beta,gamma-unsaturated amides.  34:2079-2082. 1993
  • Asymmetric-synthesis of gamma-hydroxy alpha,beta-unsaturated amides via an ad-elimination process - synthesis of (+)-coriolic acid.  34:2083-2086. 1993
  • Studies on the synthesis of bleomycin-A(2) - observations on a diastereoselective imine addition-reaction for C2-acetamido side-chain introduction.  34:1567-1570. 1993
  • Towards the synthesis of streptovaricin D: synthesis of fully elaborated aromatic precursors and coupling with ansa chain fragments.  34:1553-1556. 1993
  • Papain-catalyzed synthesis of peptide isosteres.  34:1247-1250. 1993
  • A simple route to enantiomerically enriched oxazolidin-2-ones.  34:951-952. 1993
  • Samarium diiodide hexamethylphosphoramide promoted dimerization of benzaldehydes.  34:335-338. 1993
  • Chemoenzymatic synthesis of 5-membered azasugars as inhibitors of fucosidase and fucosyl-transferase - an issue regarding the stereochemistry discrimination at transition-states.  34:403-406. 1993
  • Toward the synthesis of mycalamides A, B and onnamide A: a highly stereoselective synthesis of the trioxadecalin ring system.  34:5421-5424. 1993
  • A general-approach to gamma-lactones via osmium-catalyzed asymmetric dihydroxylation - synthesis of (-)-muricatacin and (+)-muricatacin.  33:6407-6410. 1992
  • Synthesis of all 4 isomers of disparlure using osmium-catalyzed asymmetric dihydroxylation.  33:6411-6414. 1992
  • Enantioselective synthesis of the top half of tetronolide.  33:6227-6230. 1992
  • Enantioselective synthesis of the top half of chlorothricolide.  33:4691-4694. 1992
  • A facile enzymatic-synthesis of gal-beta-1,3glucal - a key intermediate for the synthesis of le(a) and sialyl le(a).  33:4253-4256. 1992
  • Asymmetric dihydroxylation of squalene.  33:4273-4274. 1992
  • Asymmetric dihydroxylation of enynes.  33:3833-3836. 1992
  • Stereoselective synthesis of the C(13)-C(25) segment of bafilomycin A(1).  33:3587-3590. 1992
  • Asymmetric dihydroxylation of acrolein acetals - synthesis of stable equivalents of enantiopure glyceraldehyde and glycidaldehyde.  33:2095-2098. 1992
  • A new strategy for directed protein cleavage.  33:895-898. 1992
  • Studies on the synthesis of rubrolone: 4π participation of O-alkyl α,β-unsaturated oximes in intramolecular [4 + 2] cycloaddition reactions.  32:7643-7646. 1991
  • Asymmetric allylborations of 3-decynal dicobalt hexacarbonyl: cobalt induced reversal of enantioselectivity and applications to highly diastereoselective intramolecular Pauson-Khand reactions.  32:6285-6288. 1991
  • A ligand structure-enantioselectivity relationship for the osmium-catalyzed asymmetric dihydroxylation of olefins.  32:5761-5764. 1991
  • The synthesis of dibenzofuran based diacids and amino acids designed to nucleate parallel and antiparallel β-sheet formation.  32:5725-5728. 1991
  • Facile synthesis of enantiopure trans-2,3-diphenyl-1,4-diazabicyclo 2.2.2 octane.  32:4853-4854. 1991
  • Synthesis of novel disaccharides based on glycosyltransferases - beta-1,4galactosyltransferase.  32:4867-4870. 1991
  • On the timing of hydrolysis reoxidation in the osmium-catalyzed asymmetric dihydroxylation of olefins using potassium ferricyanide as the reoxidant.  32:3965-3968. 1991
  • C-phosphorylation of enolates - an alternate route to complex carbonyl-activated phosphonates.  32:2581-2584. 1991
  • Catalytic osmylation of conjugated dienes - a one-pot stereoselective synthesis of polyols.  32:1003-1006. 1991
  • Stereospecific conversion of chiral 1,2-cyclic sulfates to chiral imidazolines.  32:999-1002. 1991
  • Asymmetric cyclopropanation of alkenes catalyzed by a chiral wall porphyrin.  32:2445-2448. 1991
  • A short route to beta-lactams - use of cyclic sulfites from syn-2,3-dihydroxy esters.  31:4317-4320. 1990
  • Asymmetric allylborations of diene aldehyde Fe(CO)3 derivatives: efficient kinetic resolution of racemic complexes and the highly enantiotopic group and face selective allylboration of a meso substrate.  31:4707-4710. 1990
  • Catalysis of Diels-Alder reactions by metalloporphyrins.  31:6303-6306. 1990
  • Diisopropyl tartrate (E)-γ-(dimethylphenylsilyl)allylboronate, a chiral allylic alcohol β-carbanion equivalent for the enantioselective synthesis of 2-butene-1,4-diols from aldehydes.  31:7567-7570. 1990
  • Diisopropyl tartrate modified (E)-γ-[(cyclohexyloxy)dimethylsilyl-allylboronate, a chiral reagent for the stereoselective synthesis of anti 1,2-diols via the formal α-hydroxyallylation of aldehydes.  31:7563-7566. 1990
  • Heterogeneous catalytic asymmetric dihydroxylation - use of a polymer-bound alkaloid.  31:3003-3006. 1990
  • Ligand-based improvement of enantioselectivity in the catalytic asymmetric dihydroxylation of dialkyl substituted olefins.  31:3817-3820. 1990
  • Lipase-catalyzed irreversible transesterification using enol esters - xad-8 immobilized lipoprotein lipase-catalyzed resolution of secondary alcohols.  31:6403-6406. 1990
  • Preclusion of the 2nd cycle in the osmium-catalyzed asymmetric dihydroxylation of olefins leads to a superior process.  31:2999-3002. 1990
  • Remote functional groups enhance binding through preorganization.  31:5121-5124. 1990
  • Resolution of a CBI precursor and incorporation into the synthesis of (+)-CBI, (+)-CBI-CDPI1, (+)-CBI-CDPI2 - enhanced functional analogs of (+)-CC-1065 - a critical-appraisal of a proposed relationship between electrophile reactivity, DNA-binding properties, and cytotoxic potency.  31:793-796. 1990
  • Stereoselective synthesis of (Z,E)-2-bromo-1,3-dienes via the palladium (O) catalyzed cross coupling reactions of 1,1-dibromoolefins and vinylboronic acids.  31:6509-6512. 1990
  • Cyclic sulfates containing acid-sensitive groups and chemoselective hydrolysis of sulfate esters.  30:655-658. 1989
  • Diastereoselective synthesis of the top half of kijanolide.  30:7309-7312. 1989
  • Documenting the scope of the catalytic asymmetric dihydroxylation.  30:2041-2044. 1989
  • Lipase-catalyzed irreversible trans-esterification using enol esters - resolution of cyanohydrins and syntheses of ethyl (r)-2-hydroxy-4-phenylbutyrate and (s)-propranolol.  30:1917-1920. 1989
  • One pot synthesis of homochiral aziridines and aminoalcohols from homochiral 1,2-cyclic sulfates.  30:2623-2626. 1989
  • Stereoselective synthesis of contiguously substituted butyrolactones based on the cyclic allylsulfonium ylide rearrangement.  30:1575-1578. 1989
  • Studies on the total synthesis of fredericamycin-a - development of an intermolecular alkyne-chromium carbene complex cyclization approach to the abcde ring-system.  30:2037-2040. 1989
  • Synthesis and Diels-Alder reactions of 2-alkyl-5-methylene-1,3-dioxolan-4-ones and 2-alkyl-3-acyl-5-methylene-1,3-oxazolidin-4-ones: highly exo and diastereoface selective chiral ketene equivalents.  30:7305-7308. 1989
  • Synthesis and stereochemical assignment of the c1-c10 fragment of nystatin a1.  30:1217-1220. 1989
  • Synthesis of isodityrosine.  30:2053-2056. 1989
  • The asymmetric allylboration reaction: dependence of rate and enantioselectivity on the chiral auxiliary.  30:6457-6460. 1989
  • Total synthesis of OF4949-III and OF4949-IV - unusual effects of remote substituents on the rate of macrocyclization reactions.  30:5061-5064. 1989
  • A combined chemical and enzymatic procedure for the synthesis of 1-deoxynojirimycin and 1-deoxymannojirimycin.  29:4645-4648. 1988
  • A highly stereoselective synthesis of the octahydronaphthalene subunit of kijanolide and tetronolide.  29:3541-3544. 1988
  • Enantioselective synthesis using diisopropyl tartrate modified (E)- and (Z)-crotylboronates: reactions with achiral aldehydes.  29:5579-5582. 1988
  • One-pot tripeptide syntheses from 3 single amino-acid derivatives catalyzed by papain.  29:2907-2910. 1988
  • Synthesis of a c3-symmetric phospha 2.2.2 cyclophane.  29:5101-5104. 1988
  • Asymmetric epoxidation models - an alkyl hydroperoxide dependent change in mechanism.  28:2825-2828. 1987
  • Effect of dienophile activating group on the stereoselectivity of the intramolecular Diels-Alder reaction.  28:2447-2450. 1987
  • Further observations on the Lewis acid-catalyzed benzylic hydroperoxide rearrangement - use of a boron-trifluoride hydrogen-peroxide preformed, aged reagent.  28:1027-1030. 1987
  • Studies on the synthesis of nargenicin A(1). An example of anintramolecular Diels-Alder reaction that proceeds with a boat-likeconformation of the connecting chain.  28:931-934. 1987
  • Thermal cycloadditions of dimethyl acetylenedicarboxylate with cyclic enolethers - an entry into medium size oxocyclic systems.  28:1501-1502. 1987
  • Tohoku university series on steroids .35. Withametelin, a hexacyclic withanolide of datura-metel.  28:2025-2028. 1987
  • Total synthesis of prodigiosin.  28:2499-2502. 1987
  • Use of nonproteases in peptide-synthesis.  28:1629-1632. 1987
  • Diels-Alder cycloadditions of rigid dienophiles: a probe for allylic axial substituent control of the pi-facial selectivity in the Diels-Alder reaction.  27:683-686. 1986
  • Enzymatic aldol reaction isomerization as a route to unusual sugars.  27:1261-1264. 1986
  • Studies on the total synthesis of sesbanimide: highly diastereoselective synthesis of the AB ring system.  27:3353-3356. 1986
  • Total synthesis of 20-hydroxy-leukotrienes-b4 and 20-carboxy-leukotrienes-b4.  27:1881-1882. 1986
  • Total synthesis of the AB disaccharide unit of olivomycin A.  27:3349-3352. 1986
  • Enantioselective synthesis of the bottom half of chlorothricolide.  26:4327-4330. 1985
  • Reactions on solid supports .2. A convenient method for synthesis of pyrromethanes using a montmorillonite clay as catalyst.  26:793-796. 1985
  • Regioselective openings of 2,3-epoxy acids with organocuprates.  26:4683-4686. 1985
  • Stereochemistry of the reactions of pinacol allylboronate with two α,β-dialkoxyaldehydes.  26:3427-3430. 1985
  • The asymmetric epoxidation of tert-butyl substituted allylic alcohols.  26:2543-2546. 1985
  • Trichothecene metabolism studies. 2. Structure of 3α-​(1'β-​D-​glucopyranosiduronyl)​-​8α-​isovaleryloxyscirpen-​3,​4β,​15-​triol 15-​acetate produced from T-​2 toxin in vitro.  26:5231-5234. 1985
  • Zinc chloride-mediated conjugate reduction with silicon hydrides and palladium(0) catalyst.  26:1353-1356. 1985
  • Effective, thermal one-carbon + 2-carbon cycloaddition of cyclopropenone ketals with electron deficient olefins - cyclopropane formation.  25:5611-5614. 1984
  • Horner-Wadsworth-Emmons reaction: use of lithium chloride and an amine for base-sensitive compounds.  25:2183-2186. 1984
  • Palladium (0) mediated beta-carboline synthesis - preparation of the CDE ring-system of lavendamycin.  25:3175-3178. 1984
  • Reactions of 2,3-epoxyhalides - synthesis of optically-active allylic alcohols and homoallylic epoxides.  25:2069-2072. 1984
  • Reactions of hydroxyl-groups with "tosylchloride-dimethylaminopyridine system - direct synthesis of chlorides from hydroxycompounds.  25:2295-2296. 1984
  • Thermal, 3-carbon + 2-atom cycloaddition of cyclopropenone ketals with carbon-heteroatom double-bonds - butenolide, furan, and gamma-keto ester preparation.  25:5615-5618. 1984
  • 1,2,4-triazine preparation via thermal cycloaddition of dimethyl 1,2,4,5-tetrazine-3,6-dicarboxylate with aryl thioimidates.  24:4511-4514. 1983
  • A new synthesis of lysergic acid.  24:859-860. 1983
  • Inverse electron demand Diels-Alder reactions of 3-carbomethoxy-2-pyrones - controlled introduction of oxygenated aromatics - benzene, phenol, catechol, resorcinol, pyrogallol annulation.  24:4939-4942. 1983
  • Regioselectivity of the reactions of trialkylaluminum reagents with 2,3-epoxyalcohols: application to the synthesis of α-chiral aldehydes.  24:1377-1380. 1983
  • Stereochemistry of vinyl cuprate additions to carbohydrate-derived enones and α,β-unsaturated esters.  24:2231-2234. 1983
  • Studies on the synthesis of olivin: diastereoselective synthesis of a functionalized D-fucose derivative.  24:2227-2230. 1983
  • Synthesis of trichoverrol B.  24:3693-3696. 1983
  • An informal synthesis of +/- lysergine.  23:279-280. 1982
  • Enantioselective and stereoselective syntheses of the dihydroxyoctadienoic acid fragments of the roridins and trichoverrins.  23:3773-3776. 1982
  • Inverse electron demand diels-alder reaction of 3-carbomethoxy-2-pyrones with 1,1-dimethoxyethylene - a simple and mild method of aryl annulation.  23:4551-4554. 1982
  • Methodology for the synthesis of the acyclic portions of verrucarins A and J.  23:2331-2334. 1982
  • Organo tin nucleophiles .3. Palladium catalyzed reductive cleavage of allylic heterosubstituents with tin hydride.  23:241-244. 1982
  • Organo tin nucleophiles .4. Palladium catalyzed conjugate reduction with tin hydride.  23:477-480. 1982
  • Regiospecific total synthesis of juncusol.  23:4555-4558. 1982
  • Studies on the total synthesis of antibiotic X-14547A: the pentaene approach.  23:4879-4882. 1982
  • Synthetic analgesics - preparation of racemic 6,7-benzomorphans.  23:4559-4562. 1982
  • A mild method for the synthesis of 2-ketopyrroles from carboxylic-acids.  22:4647-4650. 1981
  • Allylstannanes as electrofugal partners in allylic alkylation.  21:2595-2598. 1980
  • Enolstannanes as electrofugal groups in allylic alkylation.  21:2591-2594. 1980
  • Intramolecular epoxidation with the H2O2/ortho ester system.  21:2491-2492. 1980
  • Large rate enhancements through preferential binding to transition states.  21:2379-2380. 1980
  • Stereoselective syntheses of substituted methyl (Z,E,E)-deca-2,7.9-trienoates and substituted methyl (Z,E,E)-undeca-2,8,10-trienoates.  21:1023-1026. 1980
  • A new class of epoxidation reagents.  1001-1002. 1979
  • New epoxidation reagents derived from alumina and silicon.  4337-4338. 1979
  • Stereoselective epoxidation of acyclic allylic alcohols - correction of our previous work.  4733-4736. 1979
  • Synthesis of 16-membered ring macrolide antibiotics .1. Stereoselective construction of the right-wing of the carbomycins and leucomycins from d-glucose.  2327-2330. 1979
  • Application of benzothiazoles to carbon-carbon bond formation in organic-synthesis.  9-12. 1978
  • Benzothiazoles as carbonyl equivalents.  5-8. 1978
  • Carbonyl participation in addition of p-chlorophenylselenenyl bromide to (e)-4-hexenal - new route to 2,6-dideoxylgycosides.  5075-5078. 1978
  • Concerning the stereochemistry of 9-methyl-Δ1-3-octalone.  17-18. 1978
  • Mutual resolution of (+)-ephedrine and z-dl-amino acid-induced by seeding chiral salt.  3813-3816. 1978
  • New and unusually flexible scheme for annulation to form fused cyclohexenone units.  4597-4600. 1978
  • New annulation processes for fused and spiro rings based on chemistry of benzothiazoles.  13-16. 1978
  • New rearrangement of n-arylhydroxamic acids catalyzed by seleninic acids and phenylselenenyl chloride.  2239-2242. 1978
  • Oxidative cationic cyclization reactions effected by pyridinium chlorochromate.  2461-2464. 1978
  • A synthetic approach to the mitosenes.  3027-3028. 1977
  • The three-phase test: the Conant-Swan reaction.  3021-3022. 1977
  • Use of phsecl in synthesis of cyclic ethers.  1257-1260. 1977
  • Vicinal acetoxychlorination of olefins by chromyl chloride in acetyl-chloride.  3523-3526. 1977
  • Ruthenium catalyzed oxidation of alcohols to aldehydes and ketones by amine-n-oxides.  2503-2506. 1976
  • Simple, stereocontrolled total synthesis of a biologically-active analog of prostaglandin endoperoxides (pgh2, pgg2).  737-740. 1976
  • Reactions of olefins with permanganate, ruthenium tetroxide, and osmium tetroxide - dependence of rate on degree of substitution.  3045-3046. 1975
  • Superoxide ion as a synthetically useful oxygen nucleophile.  3183-3186. 1975
  • Polymer-bound tosyl azide.  1391-1392. 1974
  • Short synthetic route to prostaglandins utilizing position-selective epoxide opening by vinyl gilman reagent.  2439-2440. 1974
  • Reactions of selenoxides - thermal syn-elimination and h2o-18 exchange.  1979-1982. 1973
  • Diastereomeric monocyclic diallenes. The stereochemistry of formation of racemic and meso-3,4,9,10-cyclodecatetraene-1,7-dione.  13:3425-3428. 1972
  • Mechanism of decomposition of sulfonium betaines to epoxides.  13:3313-3316. 1972
  • On the absolute configuration of toxol at c-3. Vicinal h-h coupling constants in 2-alkyl-3-hydroxydihydrobenzofurans.  13:2873-2876. 1972
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Identity

International Standard Serial Number (ISSN)

  • 0040-4039

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