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Cyclopentanes

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  • A highly diastereo- and enantioselective synthesis of multisubstituted cyclopentanes with four chiral carbons by the organocatalytic domino Michael-Henry reaction  Academic Article
  • A rab1 mutant affecting guanine-nucleotide exchange promotes disassembly of the golgi-apparatus  Academic Article
  • A synthesis of echinopine B  Academic Article
  • An inhibitor of NEDD8-activating enzyme as a new approach to treat cancer  Academic Article
  • Antibody-catalyzed reversal of chemoselectivity  Academic Article
  • Benzylidene cyclopentenediones: First irreversible inhibitors against botulinum neurotoxin A's zinc endopeptidase  Academic Article
  • Catalytic and regioselective ring expansion of arylcyclobutanones with trimethylsilyldiazomethane. Ligand-dependent entry to beta-ketosilane or enolsilane adducts  Academic Article
  • Control of four stereocenters in an organocatalytic domino double Michael reaction: Efficient synthesis of multisubstituted cyclopentanes  Academic Article
  • Core-structure-motivated design of a phosphine-catalyzed 3+2 cycloaddition reaction: Enantioselective syntheses of spirocyclopenteneoxindoles  Academic Article
  • Diastereoselective synthesis of vicinal tertiary diols  Academic Article
  • Different plant hormones regulate similar processes through largely nonoverlapping transcriptional responses  Academic Article
  • Ecological modulation of plant defense via phytochrome control of jasmonate sensitivity  Academic Article
  • Expression profile matrix of Arabidopsis transcription factor genes suggests their putative functions in response to environmental stresses  Academic Article
  • First synthesis and structural elucidation of (-)-presphaerene  Academic Article
  • Hepatitis B virus (HBV)-specific cytotoxic T-cell (CTL) response in humans: characterization of HLA class II-restricted CTLs that recognize endogenously synthesized HBV envelope antigens  Academic Article
  • Induced responses to herbivory and jasmonate in three milkweed species  Academic Article
  • Intramolecular Diels-Alder reactions of siloxacyclopentene constrained trienes  Academic Article
  • Quality-control in the endoplasmic-reticulum - folding and misfolding of vesicular stomatitis-virus g-protein in cells and in vitro  Academic Article
  • Siloxacyclopentenes as dienophile-linked directing groups in intramolecular Diels-Alder reactions  Academic Article
  • Structural basis of JAZ repression of MYC transcription factors in jasmonate signalling  Academic Article
  • Structure-kinetic relationships--an overlooked parameter in hit-to-lead optimization: a case of cyclopentylamines as chemokine receptor 2 antagonists  Academic Article
  • Substrate-assisted inhibition of ubiquitin-like protein-activating enzymes: the NEDD8 E1 inhibitor MLN4924 forms a NEDD8-AMP mimetic in situ  Academic Article
  • Synthesis and applications of Hajos-Parrish ketone isomers  Academic Article
  • Synthesis and applications of a deep, asymmetric cavitand on a solid support  Academic Article
  • Synthesis of neplanocin A and its 3'-epimer via an intramolecular Baylis-Hillman reaction  Academic Article
  • Tetrahydro anthranilic acid as a surrogate for anthranilic acid: application to the discovery of potent niacin receptor agonists  Academic Article
  • The cyclopentenone product of lipid peroxidation, 15-A(2t)-isoprostane (8-isoprostaglandin A(2)), is efficiently conjugated with glutathione by human and rat glutathione transferase A4-4  Academic Article
  • The de-guanidinylated derivative of peramivir remains a potent inhibitor of influenza neuraminidase  Academic Article
  • The vinylogous intramolecular Morita-Baylis-Hillman reaction: synthesis of functionalized cyclopentenes and cyclohexenes with trialkylphosphines as nucleophilic catalysts  Academic Article
  • Total synthesis of cochleamycin A  Academic Article
  • Total synthesis of Δ¹²-prostaglandin J₃, a highly potent and selective antileukemic agent  Academic Article
  • When structure-affinity relationships meet structure-kinetics relationships: 3-((Inden-1-yl)amino)-1-isopropyl-cyclopentane-1-carboxamides as CCR2 antagonists  Academic Article

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