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Snyder, Scott
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Snyder, Scott

Associate Professor Adjunct
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Positions

  • 2015 - Professor of Chemistry, The University of Chicago
  • 2015 - Associate Professor Adjunct, Chemistry , Scripps Research
  • 2013 - 2015 Associate Professor, with tenure, Chemistry , Scripps Research
  • 2011 - 2013 Associate Professor, without tenure, Columbia University
  • 2006 - 2011 Assistant Professor, Columbia University
  • 2004 - 2006 NIH Postdoctoral Fellow with Dr. E. J. Corey, Harvard University

Research Areas research areas

  • natural products (UMLS)

Contact

  • ssnyder@scripps.edu

Websites

  • Doctoral Dissertation
  • Publications
  • Teaching
  • Background
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  • Identity
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Publications

recent publications
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  • Publications without PubMed PMIDs

  • academic article

    • Ozog, S., Timberlake, N. D., Hermann, K., Garijo, O., Haworth, K. G., Shi, G., Glinkerman, C. M., Schefter, L. E., D'Souza, S., Simpson, E., Sghia-Hughes, G., Carillo, R. R., et al. Resveratrol trimer enhances gene delivery to hematopoietic stem cells by reducing antiviral restriction at endosomes Blood  2019 134:1298-1311  DOI:10.1182/blood.2019000040  PMID:31416800
    • Hu, P., Chi, H. M., DeBacker, K. C., Gong, X., Keim, J. H., Hsu, I. T., Snyder, S. A. Quaternary-centre-guided synthesis of complex polycyclic terpenes Nature  2019 569:703-707  DOI:10.1038/s41586-019-1179-2  PMID:31022719
    • Zhang, Y. A., Yaw, N., Snyder, S. A. General synthetic approach for the Laurencia family of natural products empowered by a potentially biomimetic ring expansion Journal of the American Chemical Society  2019 141:7776-7788  DOI:10.1021/jacs.9b01088  PMID:30998347
    • Zhou, Z., Gao, A. X., Snyder, S. A. Total synthesis of (+)-arborisidine Journal of the American Chemical Society  2019 141:7715-7720  DOI:10.1021/jacs.9b03248  PMID:31017434
    • Yang, M., Yin, F., Fujino, H., Snyder, S. A. The total synthesis of chalcitrin Journal of the American Chemical Society  2019 141:4515-4520  DOI:10.1021/jacs.8b12612  PMID:30813728
    • Lisnyak, V. G., Lynch-Colameta, T., Snyder, S. A. Mannich-type reactions of cyclic nitrones: effective methods for the enantioselective synthesis of piperidine-containing alkaloids Angewandte Chemie-International Edition  2018 57:15162-15166  DOI:10.1002/anie.201809799  PMID:30276949
    • Cole, C. J. F., Chi, H. M., DeBacker, K. C., Snyder, S. A. Synthesis of enhanced, isolable disulfanium salts and their application to thiiranium-promoted polyene cyclizations Synthesis-Stuttgart  2018 50:4351-4358  DOI:10.1055/s-0037-1609754
    • Gan, P., Pitzen, J., Qu, P., Snyder, S. A. Total synthesis of the caged indole alkaloid arboridinine enabled by aza-Prins and metal-mediated cyclizations Journal of the American Chemical Society  2018 140:919-925  DOI:10.1021/jacs.7b07724  PMID:29309137
    • Ye, Q., Qu, P., Snyder, S. A. Total syntheses of scaparvins B, C, and D enabled by a Key C-H functionalization Journal of the American Chemical Society  2017 139:18428-18431  DOI:10.1021/jacs.7b06185  PMID:29227651
    • Schevenels, F. T., Shen, M., Snyder, S. A. Isolable and readily handled halophosphonium pre-reagents for hydro- and deuteriohalogenation Journal of the American Chemical Society  2017 139:6329-6337  DOI:10.1021/jacs.6b12653  PMID:28462991
    • Hu, P., Snyder, S. A. Enantiospecific total synthesis of the highly strained (-)-presilphiperfolan-8-ol via a Pd-catalyzed tandem cyclization Journal of the American Chemical Society  2017 139:5007-5010  DOI:10.1021/jacs.7b01454  PMID:28355073
    • Snyder, S. A., Porco, J. A. Advancing science through synthetic chemistry and chemical biology: special issue in honor of the 2016 Wolf prize laureates in chemistry, Professors Kyriacos C. Nicolaou and Stuart L. Schreiber Israel Journal of Chemistry  2017 57:173-173  DOI:10.1002/ijch.201700010
    • Smith, M. W., Zhou, Z., Gao, A. X., Shimbayashi, T., Snyder, S. A. A 7-step formal asymmetric total synthesis of strictamine via an asymmetric propargylation and metal-mediated cyclization Organic Letters  2017 19:1004-1007  DOI:10.1021/acs.orglett.6b03839  PMID:28253628
    • Schevenels, F. T., Shen, M., Snyder, S. A. Alkyldisulfanium salts: isolable, electrophilic sulfur reagents competent for polyene cyclizations Organic Letters  2017 19:2-5  DOI:10.1021/acs.orglett.6b02059  PMID:27973855
    • Snyder, S. A. Strategies and tactics for the synthesis of complex alkaloids Chimia  2017 71:802-809  DOI:10.2533/chimia.2017.802  PMID:29289241
    • Shen, M., Kretschmer, M., Brill, Z. G., Snyder, S. A. Strategies for the total synthesis of diverse bromo-chamigrenes Organic Letters  2016 18:5018-5021  DOI:10.1021/acs.orglett.6b02478  PMID:27660885
    • Gao, A. X., Hamada, T., Snyder, S. A. The enantioselective total synthesis of exochomine Angewandte Chemie-International Edition  2016 55:10301-10306  DOI:10.1002/anie.201604744  PMID:27443416
    • Gan, P., Smith, M. W., Braffman, N. R., Snyder, S. A. Pyrone Diels-Alder routes to indolines and hydroindolines: syntheses of gracilamine, mesembrine, and Δ(7) -mesembrenone Angewandte Chemie-International Edition  2016 55:3625-3630  DOI:10.1002/anie.201510520  PMID:26865400
    • Eagan, J. M., Hori, M., Wu, J., Kanyiva, K. S., Snyder, S. A. Synthesis and applications of Hajos-Parrish ketone isomers Angewandte Chemie-International Edition  2015 54:7842-7846  DOI:10.1002/anie.201500925  PMID:25974879  PMCID:PMC4737474
    • Levinson, A. M., Milner, P. J., Snyder, S. A. Studies in selective 6-membered bromoether formation via bromonium and thiiranium-induced cyclizations Tetrahedron Letters  2015 56:3553-3556  DOI:10.1016/j.tetlet.2015.02.065
    • Quideau, S., Snyder, S. A. Chemistry in the vine and wine sciences Preface Tetrahedron  2015 71:2969-2970  DOI:10.1016/j.tet.2015.02.086
    • Wright, N. E., ElSohly, A. M., Snyder, S. A. Syntheses of cyclotriveratrylene analogues and their long elusive triketone congeners Organic Letters  2014 16:3644-3647  DOI:10.1021/ol501284s  PMID:24987807  PMCID:PMC4334237
    • Sherwood, T. C., Trotta, A. H., Snyder, S. A. A strategy for complex dimer formation when biomimicry fails: total synthesis of ten coccinellid alkaloids Journal of the American Chemical Society  2014 136:9743-9753  DOI:10.1021/ja5045852  PMID:24959981  PMCID:PMC4105056
    • Snyder, S. A., Berova, N. Asymmetric alkene halogenation Chirality  2014 26:327-327  DOI:10.1002/chir.22345  PMID:24946765
    • Jepsen, T. H., Thomas, S. B., Lin, Y., Stathakis, C. I., de Miguel, I., Snyder, S. A. Harnessing quinone methides: total synthesis of (+/-)-vaticanol A Angewandte Chemie-International Edition  2014 53:6747-6751  DOI:10.1002/anie.201402858  PMID:24841889  PMCID:PMC4106016
    • Wright, N. E., Snyder, S. A. 9-membered carbocycle formation: development of distinct Friedel-Crafts cyclizations and application to a scalable total synthesis of ( +/-)- caraphenol A Angewandte Chemie-International Edition  2014 53:3409-3413  DOI:10.1002/anie.201311299  PMID:24677499  PMCID:PMC4106019
    • Griffith, D. R., Botta, L., St Denis, T. G., Snyder, S. A. Explorations of caffeic acid derivatives: total syntheses of rufescenolide, yunnaneic acids C and D, and studies toward yunnaneic acids A and B Journal of Organic Chemistry  2014 79:88-105  DOI:10.1021/jo4023167  PMID:24328186
    • Brucks, A. P., Treitler, D. S., Liu, S. A., Snyder, S. A. Explorations into the potential of chiral sulfonium reagents to effect asymmetric halonium additions to isolated alkenes Synthesis-Stuttgart  2013 45:1886-1898  DOI:10.1055/s-0033-1338865
    • Treitler, D. S., Li, Z. F., Krystal, M., Meanwell, N. A., Snyder, S. A. Evaluation of HIV-1 inhibition by stereoisomers and analogues of the sesquiterpenoid hydroquinone peyssonol A Bioorganic & Medicinal Chemistry Letters  2013 23:2192-2196  DOI:10.1016/j.bmcl.2013.01.098  PMID:23434230
    • ElSohly, A. M., Wespe, D. A., Poore, T. J., Snyder, S. A. An efficient approach to the securinega alkaloids empowered by cooperative N-heterocyclic carbene/Lewis acid catalysis Angewandte Chemie - International Edition  2013 52:5789-5794  DOI:10.1002/anie.201301849  PMID:23610056
    • Snyder, S. A., Brucks, A. P., Treitler, D. S., Moga, I. Concise synthetic approaches for the Laurencia family: formal total syntheses of (±)-laurefucin and (±)-E- and (±)-Z-pinnatifidenyne Journal of the American Chemical Society  2012 134:17714-17721  DOI:10.1021/ja3076988  PMID:23057834
    • Snyder, S. A., Kontes, F., ElSohly, A. M. Mechanistic investigations of the cyclocondensation step of the Knorr pyrrole synthesis Heterocycles  2012 84:265-274  DOI:10.3987/com-11-s(p)5
    • Snyder, S. A., Thomas, S. B., Mayer, A. C., Breazzano, S. P. Total syntheses of hopeanol and hopeahainol A empowered by a chiral Brønsted acid induced pinacol rearrangement Angewandte Chemie-International Edition  2012 51:4080-4084  DOI:10.1002/anie.201107730  PMID:22431237  PMCID:PMC3744884
    • Snyder, S. A., Brill, Z. G. Structural revision and total synthesis of caraphenol B and C Organic Letters  2011 13:5524-5527  DOI:10.1021/ol2022406  PMID:21942557  PMCID:PMC3224822
    • Snyder, S. A., Treitler, D. S., Brucks, A. P., Sattler, W. A general strategy for the stereocontrolled preparation of diverse 8- and 9-membered Laurencia-type bromoethers Journal of the American Chemical Society  2011 133:15898-15901  DOI:10.1021/ja2069449  PMID:21919540
    • Snyder, S. A., Gollner, A., Chiriac, M. I. Regioselective reactions for programmable resveratrol oligomer synthesis Nature  2011 474:461-466  DOI:10.1038/nature10197  PMID:21697944  PMCID:PMC3179663
    • Snyder, S. A., Wespe, D. A., von Hof, J. M. A concise, stereocontrolled total synthesis of rippertenol Journal of the American Chemical Society  2011 133:8850-8853  DOI:10.1021/ja202859f  PMID:21574654
    • Snyder, S. A. Natural product synthesis: Making nematodes nervous Nature Chemistry  2011 3:422-423  DOI:10.1038/nchem.1059  PMID:21602850
    • Snyder, S. A., Kontes, F. Synthetic studies of biomimetic Diels-Alder processes toward the helicterin family of natural products Israel Journal of Chemistry  2011 51:378-390  DOI:10.1002/ijch.201100004
    • Snyder, S. A., Treitler, D. S., Satoh, N., Fukuyama, T. Synthesis of Et2SBr•SbCI5Br and its use in biomimetic brominative polyene cyclizations Organic Syntheses  2011 88:54-69  DOI:10.1002/0471264229.os088.06
    • Snyder, S. A., ElSohly, A. M., Kontes, F. Synthetic approaches to oligomeric natural products Natural Product Reports  2011 28:897-924  DOI:10.1039/c1np00001b  PMID:21412558
    • Snyder, S. A., Wright, N. E., Pflueger, J. J., Breazzano, S. P. Total syntheses of heimiol A, hopeahainol D, and constrained analogues Angewandte Chemie-International Edition  2011 50:8629-8633  DOI:10.1002/anie.201103575  PMID:21793142  PMCID:PMC3263399
    • Snyder, S. A., Treitler, D. S., Brucks, A. P. Simple reagents for direct halonium-induced polyene cyclizations Journal of the American Chemical Society  2010 132:14303-14314  DOI:10.1021/ja106813s  PMID:20858010
    • Snyder, S. A., Treitler, D. S., Schall, A. A two-step mimic for direct, asymmetric bromonium- and chloronium-induced polyene cyclizations Tetrahedron  2010 66:4796-4804  DOI:10.1016/j.tet.2010.03.037
    • Snyder, S. A. Organic chemistry: Symmetrizing the unsymmetrical Nature  2010 465:560-561  DOI:10.1038/465560a  PMID:20520702
    • Welsch, M. E., Snyder, S. A., Stockwell, B. R. Privileged scaffolds for library design and drug discovery Current Opinion in Chemical Biology  2010 14:347-361  DOI:10.1016/j.cbpa.2010.02.018  PMID:20303320  PMCID:PMC2908274
    • Snyder, S. A., ElSohly, A. M., Kontes, F. Synthetic and theoretical investigations of myrmicarin biosynthesis Angewandte Chemie-International Edition  2010 49:9693-9698  DOI:10.1002/anie.201005825  PMID:21069649
    • Snyder, S. A., Sherwood, T. C., Ross, A. G. Total syntheses of dalesconol A and B Angewandte Chemie-International Edition  2010 49:5146-5150  DOI:10.1002/anie.201002264  PMID:20572237  PMCID:PMC3075011
    • Pors, K., Goldberg, F. W., Leamon, C. P., Rigby, A. C., Snyder, S. A., Falconer, R. A. The changing landscape of cancer drug discovery: a challenge to the medicinal chemist of tomorrow Drug Discovery Today  2009 14:1045-1050  DOI:10.1016/j.drudis.2009.07.004  PMID:19638319
    • Snyder, S. A., Tang, Z. Y., Gupta, R. Enantioselective total synthesis of (-)-napyradiomycin A1 via asymmetric chlorination of an isolated olefin Journal of the American Chemical Society  2009 131:5744-5745  DOI:10.1021/ja9014716  PMID:19338329
    • Snyder, S. A., Kontes, F. Explorations into neolignan biosynthesis: concise total syntheses of helicterin B, helisorin, and helisterculin A from a common intermediate Journal of the American Chemical Society  2009 131:1745-1752  DOI:10.1021/ja806865u  PMID:19191699
    • Snyder, S. A.*, Breazzano, S. P.*, Ross, A. G., Lin, Y., Zografos, A. L. Total synthesis of diverse carbogenic complexity within the resveratrol class from a common building block Journal of the American Chemical Society  2009 131:1753-1765  DOI:10.1021/ja806183r  PMID:19143488 (* = equal contribution)
    • Snyder, S. A., Treitler, D. S. Et2SBrSbCl5Br: an effective reagent for direct bromonium-induced polyene cyclizations Angewandte Chemie-International Edition  2009 48:7899-7903  DOI:10.1002/anie.200903834  PMID:19757473
    • Snyder, S. A., Zografos, A. L., Lin, Y. Total synthesis of resveratrol-based natural products: A chemoselective solution Angewandte Chemie-International Edition  2007 46:8186-8191  DOI:10.1002/anie.200703333  PMID:17890663
    • Snyder, S. A., Corey, E. J. Regioselective aldol condensations of a cholestanone-derived dialdehyde: new twists on a classic reaction Tetrahedron Letters  2006 47:2083-2086  DOI:10.1016/j.tetlet.2006.01.136
    • Snyder, S. A., Corey, E. J. Concise total syntheses of palominol, dolabellatrienone, beta-araneosene, and isoedunol via an enantioselective Diels-Alder macrobicyclization Journal of the American Chemical Society  2006 128:740-742  DOI:10.1021/ja0576379  PMID:16417362
    • Snyder, S. A. From abyssomicin to zaragozic acid: Chemical synthesis and drug innovation Angewandte Chemie-International Edition  2006 45:4714-4714  DOI:10.1002/anie.200602427
    • degree-related publication Nicolaou, K. C.*, Snyder, S. A.* Chasing molecules that were never there: Misassigned natural products and the role of chemical synthesis in modern structure elucidation Angewandte Chemie-International Edition  2005 44:1012-1044  DOI:10.1002/anie.200460864  PMID:15688428 (* = equal contribution)
    • degree-related publication Nicolaou, K. C.*, Snyder, S. A.*, Longbottom, D. A., Nalbandian, A. Z., Huang, X. H. New uses for the burgess reagent in chemical synthesis: Methods for the facile and stereoselective formation of sulfamidates, glycosylamines, and sulfamides Chemistry-a European Journal  2004 10:5581-5606  DOI:10.1002/chem.200400503  PMID:15470695 (* = equal contribution)
    • degree-related publication Nicolaou, K. C.*, Snyder, S. A.*, Huang, X. H., Simonsen, K. B., Koumbis, A. E., Bigot, A. Studies toward diazonamide A: Initial synthetic forays directed toward the originally proposed structure Journal of the American Chemical Society  2004 126:10162-10173  DOI:10.1021/ja040090y  PMID:15303892 (* = equal contribution)
    • degree-related publication Nicolaou, K. C.*, Snyder, S. A.* The essence of total synthesis Proceedings of the National Academy of Sciences of the United States of America  2004 101:11929-11936  DOI:10.1073/pnas.0403799101  PMID:15302925  PMCID:PMC514411 (* = equal contribution)
    • degree-related publication Nicolaou, K. C.*, Snyder, S. A.*, Nalbandian, A. Z., Longbottom, D. A. A new method for the stereoselective synthesis of α- and β-glycosylamines using the burgess reagent Journal of the American Chemical Society  2004 126:6234-6235  DOI:10.1021/ja049293c  PMID:15149212 (* = equal contribution)
    • degree-related publication Nicolaou, K. C., Chen, D. Y. K., Huang, X. H., Ling, T. T., Bella, M., Snyder, S. A. Chemistry and biology of diazonamide A: First total synthesis and confirmation of the true structure Journal of the American Chemical Society  2004 126:12888-12896  DOI:10.1021/ja040092i  PMID:15469286
    • degree-related publication Nicolaou, K. C., Hao, J. L., Reddy, M. V., Rao, P. B., Rassias, G., Snyder, S. A., Huang, X. H., Chen, D. Y. K., Brenzovich, W. E., Giuseppone, N., Giannakakou, P., O'Brate, A. Chemistry and biology of diazonamide A: Second total synthesis and biological investigations Journal of the American Chemical Society  2004 126:12897-12906  DOI:10.1021/ja040093a  PMID:15469287
    • degree-related publication Nicolaou, K. C.*, Snyder, S. A.*, Giuseppone, N., Huang, X. H., Bella, M., Reddy, M. V., Rao, P. B., Koumbis, A. E., Giannakakou, P., O'Brate, A. Studies toward diazonamide A: Development of a hetero-pinacol macrocyclization cascade for the construction of the bis-macrocyclic framework of the originally proposed structure Journal of the American Chemical Society  2004 126:10174-10182  DOI:10.1021/ja040091q  PMID:15303893 (* = equal contribution)
    • degree-related publication Nicolaou, K. C.*, Snyder, S. A.* Cascade reactions in total synthesis. Recent advances Actualite Chimique  2003 83-88 (* = equal contribution)
    • degree-related publication Nicolaou, K. C., Montagnon, T., Snyder, S. A. Tandem reactions, cascade sequences, and biomimetic strategies in total synthesis Chemical Communications  2003 551-564  DOI:10.1039/b209440c
    • degree-related publication Nicolaou, K. C., Rao, P. B., Hao, J. L., Reddy, M. V., Rassias, G., Huang, X. H., Chen, D. Y. K., Snyder, S. A. The second total synthesis of diazonamide A Angewandte Chemie-International Edition  2003 42:1753-1758  DOI:10.1002/anie.200351112  PMID:12707898
    • degree-related publication Nicolaou, K. C., Longbottom, D. A., Snyder, S. A., Nalbanadian, A. Z., Huang, X. H. A new method for the synthesis of nonsymmetrical sulfamides using burgess-type reagents Angewandte Chemie-International Edition  2002 41:3866-3870  DOI:10.1002/1521-3773(20021018)41:20<3866::aid-anie3866>3.0.co;2-t  PMID:12386873
    • degree-related publication Nicolaou, K. C., Huang, X. H., Snyder, S. A., Rao, P. B., Bella, M., Reddy, M. V. A novel regio- and stereoselective synthesis of sulfamidates from 1,2-diols using burgess and related reagents: A facile entry into β-amino alcohols Angewandte Chemie-International Edition  2002 41:834-838  DOI:10.1002/1521-3773(20020301)41:5<834::aid-anie834>3.0.co;2-v  PMID:12491352
    • degree-related publication Nicolaou, K. C.*, Snyder, S. A.*, Montagnon, T., Vassilikogiannakis, G. The Diels-Alder reaction in total synthesis Angewandte Chemie-International Edition  2002 41:1668-1698  DOI:10.1002/1521-3773(20020517)41:10<1668::aid-anie1668>3.0.co;2-z  PMID:19750686 (* = equal contribution)
    • degree-related publication Nicolaou, K. C., Bella, M., Chen, D. Y. K., Huang, X. H., Ling, T. T., Snyder, S. A. Total synthesis of diazonamide A Angewandte Chemie-International Edition  2002 41:3495-3499  DOI:10.1002/1521-3773(20020916)41:18<3495::aid-anie3495>3.0.co;2-7  PMID:12298077
    • degree-related publication Nicolaou, K. C., Huang, X., Giuseppone, N., Rao, P. B., Bella, M., Reddy, M. V., Snyder, S. A. Construction of the complete aromatic core of diazonamide a by a novel hetero pinacol macrocyclization cascade reaction Angewandte Chemie-International Edition  2001 40:4705-4709  DOI:10.1002/1521-3773(20011217)40:24<4705::aid-anie4705>3.0.co;2-d  PMID:12404390
    • Markgraf, J. H., Sangani, P. K., Manalansan, R. J., Snyder, S. A., Thummel, R. P. Strained heterocyclic systems. Part 21. The Menschutkin reaction Journal of Chemical Research-S  2000 2000:561-563  DOI:10.3184/030823400103166184
    • Snyder, S. A., Vosburg, D. A., Jarvis, M. G., Markgraf, J. H. Intramolecular hetero Diels-Alder routes to γ-carboline alkaloids Tetrahedron  2000 56:5329-5335  DOI:10.1016/s0040-4020(00)00468-3
    • degree-related publication Nicolaou, K. C.*, Snyder, S. A.*, Simonsen, K. B., Koumbis, A. E. Model studies towards diazonamide A: Synthesis of the heterocyclic core Angewandte Chemie-International Edition  2000 39:3473-3478  DOI:10.1002/1521-3773(20001002)39:19<3473::aid-anie3473>3.0.co;2-e  PMID:11091394 (* = equal contribution)
    • degree-related publication Nicolaou, K. C., Koumbis, A. E., Snyder, S. A., Simonsen, K. B. Novel reactions initiated by titanocene methylidenes: Deoxygenation of sulfoxides, n-oxides, and selenoxides Angewandte Chemie-International Edition  2000 39:2529-2533  DOI:10.1002/1521-3773(20000717)39:14<2529::aid-anie2529>3.0.co;2-e  PMID:10941126
    • degree-related publication Nicolaou, K. C.*, Snyder, S. A.*, Bigot, A., Pfefferkorn, J. A. Solution and solid-phase synthesis of functionalized 3-arylbenzofurans by a novel cyclofragmentation-release pathway Angewandte Chemie-International Edition  2000 39:1093-1096  DOI:10.1002/(sici)1521-3773(20000317)39:6<1093::aid-anie1093>3.3.co;2-j  PMID:10760931 (* = equal contribution)
    • Markgraf, J. H., Snyder, S. A., Vosburg, D. A. A concise route to isocanthin-6-one Tetrahedron Letters  1998 39:1111-1112  DOI:10.1016/s0040-4039(97)10794-8
    • Cao, F. L., Eckert, R., Elfgang, C., Nitsche, J. M., Snyder, S. A., Hulser, D. F., Willecke, K., Nicholson, B. J. A quantitative analysis of connexin-specific permeability differences of gap junctions expressed in HeLa transfectants and Xenopus oocytes Journal of Cell Science  1998 111:31-43  PMID:9394010
  • book

    • Solomons, T. W. Graham, Fryhle, Craig B., Snyder, S. A. Organic chemistry 2016
    • degree-related publication Nicolaou, K. C.*, Snyder, Scott A.* Classics in total synthesis II : more targets, strategies, methods Weinheim: Wiley-VCH. 2003 (* = equal contribution)
  • chapter

    • Gao, A. X., Thomas, S. B., Snyder, S. A. Pinacol and semipinacol rearrangements in total synthesis Molecular Rearrangements in Organic Synthesis. 1-34. 2015  DOI:10.1002/9781118939901.ch1

featured in

  • Scripps Research Institute Appoints Columbia University Scientist to Chemistry Department  News Release
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Teaching

advisees

  • graduate advising relationship

    • Gan, Pei, Ph.D.  candidate, 2013 - 2017
    • Gao, Alison, Ph.D.  candidate, 2012 - 2017
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Background

education and training

  • Ph.D. in Chemistry, Scripps Research 1999 - 2004
  • B.A. in Chemistry, Williams College , with highest honors in Chemistry, Summa Cum Laude, valedictorian. Advisor: Dr. J. H. Markgraf 1995 - 1999

advisee of

  • graduate advising relationship

    • Nicolaou, K.C., Ph.D.  candidacy, 2000 - 2004
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Contact

full name

  • Scott A. Snyder

geographic location

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