Scott A. Snyder - Publications

Affiliations: 
Chemistry University of Chicago, Chicago, IL 
Area:
total synthesis of natural products
Website:
http://snyder-group.uchicago.edu/

80 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2019 Yi H, Hu P, Snyder SA. Development and Elucidation of a Pd-based Cyclization/Oxygenation Sequence for Natural Product Synthesis. Angewandte Chemie (International Ed. in English). PMID 31742828 DOI: 10.1002/anie.201913730  0.32
2019 Hu P, Chi HM, DeBacker KC, Gong X, Keim JH, Hsu IT, Snyder SA. Quaternary-centre-guided synthesis of complex polycyclic terpenes. Nature. PMID 31022719 DOI: 10.1038/s41586-019-1179-2  0.32
2019 Zhang YA, Yaw N, Snyder SA. A General Synthetic Approach for the Laurencia Family of Natural Products Empowered by a Potentially Biomimetic Ring Expansion. Journal of the American Chemical Society. PMID 30998347 DOI: 10.1021/jacs.9b01088  1
2018 Gan P, Pitzen J, Qu P, Snyder SA. Total Synthesis of the Caged Indole Alkaloid Arboridinine Enabled by aza-Prins and Metal-Mediated Cyclizations. Journal of the American Chemical Society. PMID 29309137 DOI: 10.1021/jacs.7b07724  0.72
2017 Ye Q, Qu P, Snyder SA. Total Syntheses of Scaparvins B, C, and D Enabled by a Key C-H Functionalization. Journal of the American Chemical Society. 139: 18428-18431. PMID 29227651 DOI: 10.1021/jacs.7b06185  0.72
2017 Hu P, Snyder SA. Enantiospecific Total Synthesis of the Highly Strained (-)-Presilphiperfolan-8-ol via a Pd-Catalyzed Tandem Cyclization. Journal of the American Chemical Society. PMID 28355073 DOI: 10.1021/jacs.7b01454  0.32
2016 Shen M, Kretschmer M, Brill ZG, Snyder SA. Strategies for the Total Synthesis of Diverse Bromo-Chamigrenes. Organic Letters. PMID 27660885 DOI: 10.1021/acs.orglett.6b02478  1
2016 Gao AX, Hamada T, Snyder SA. The Enantioselective Total Synthesis of Exochomine. Angewandte Chemie (International Ed. in English). PMID 27443416 DOI: 10.1002/anie.201604744  1
2016 Gan P, Smith MW, Braffman NR, Snyder SA. Pyrone Diels-Alder Routes to Indolines and Hydroindolines: Syntheses of Gracilamine, Mesembrine, and Δ(7) -Mesembrenone. Angewandte Chemie (International Ed. in English). PMID 26865400 DOI: 10.1002/anie.201510520  1
2015 Eagan JM, Hori M, Wu J, Kanyiva KS, Snyder SA. Synthesis and Applications of Hajos-Parrish Ketone Isomers. Angewandte Chemie (International Ed. in English). 54: 7842-6. PMID 25974879 DOI: 10.1002/anie.201500925  1
2015 Quideau S, Snyder SA. Chemistry in the vine and wine sciences Tetrahedron. DOI: 10.1016/j.tet.2015.02.086  1
2015 Quideau S, Snyder SA. Professors Stéphane Quideau and Scott A. Snyder Tetrahedron. DOI: 10.1016/j.tet.2015.02.085  1
2014 Wright NE, ElSohly AM, Snyder SA. Syntheses of cyclotriveratrylene analogues and their long elusive triketone congeners. Organic Letters. 16: 3644-7. PMID 24987807 DOI: 10.1021/ol501284s  1
2014 Sherwood TC, Trotta AH, Snyder SA. A strategy for complex dimer formation when biomimicry fails: total synthesis of ten coccinellid alkaloids. Journal of the American Chemical Society. 136: 9743-53. PMID 24959981 DOI: 10.1021/ja5045852  1
2014 Snyder SA, Berova N. Asymmetric alkene halogenation. Chirality. 26: 327. PMID 24946765 DOI: 10.1002/chir.22345  0.52
2014 Jepsen TH, Thomas SB, Lin Y, Stathakis CI, de Miguel I, Snyder SA. Harnessing quinone methides: total synthesis of (±)-vaticanol A. Angewandte Chemie (International Ed. in English). 53: 6747-51. PMID 24841889 DOI: 10.1002/anie.201402858  1
2014 Wright NE, Snyder SA. 9-Membered carbocycle formation: development of distinct Friedel-Crafts cyclizations and application to a scalable total synthesis of (±)-caraphenol A. Angewandte Chemie (International Ed. in English). 53: 3409-13. PMID 24677499 DOI: 10.1002/anie.201311299  1
2014 Griffith DR, Botta L, St Denis TG, Snyder SA. Explorations of caffeic acid derivatives: total syntheses of rufescenolide, yunnaneic acids C and D, and studies toward yunnaneic acids A and B. The Journal of Organic Chemistry. 79: 88-105. PMID 24328186 DOI: 10.1021/jo4023167  1
2014 Levinson AM, Milner PJ, Snyder SA. Studies in selective 6-membered bromoether formation via bromonium and thiiranium-induced cyclizations Tetrahedron Letters. DOI: 10.1016/j.tetlet.2015.02.065  1
2014 Snyder SA, Levinson AM. Polyene Cyclizations Comprehensive Organic Synthesis: Second Edition. 3: 268-292. DOI: 10.1016/B978-0-08-097742-3.00309-8  1
2013 Smith MW, Snyder SA. A concise total synthesis of (+)-scholarisine A empowered by a unique C-H arylation. Journal of the American Chemical Society. 135: 12964-7. PMID 23964983 DOI: 10.1021/ja406546k  1
2013 ElSohly AM, Wespe DA, Poore TJ, Snyder SA. An efficient approach to the securinega alkaloids empowered by cooperative N-heterocyclic carbene/Lewis acid catalysis. Angewandte Chemie (International Ed. in English). 52: 5789-94. PMID 23610056 DOI: 10.1002/anie.201301849  1
2013 Treitler DS, Li Z, Krystal M, Meanwell NA, Snyder SA. Evaluation of HIV-1 inhibition by stereoisomers and analogues of the sesquiterpenoid hydroquinone peyssonol A. Bioorganic & Medicinal Chemistry Letters. 23: 2192-6. PMID 23434230 DOI: 10.1016/j.bmcl.2013.01.098  1
2013 Brucks AP, Treitler DS, Liu SA, Snyder SA. Explorations into the potential of chiral sulfonium reagents to effect asymmetric halonium additions to isolated alkenes Synthesis (Germany). 45: 1886-1898. DOI: 10.1055/s-0033-1338865  1
2013 Snyder SA, Brucks AP. Asymmetric Halonium Addition to Olefins Asymmetric Synthesis Ii: More Methods and Applications. 147-155. DOI: 10.1002/9783527652235.ch20  1
2012 Snyder SA, Brucks AP, Treitler DS, 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. 134: 17714-21. PMID 23057834 DOI: 10.1021/ja3076988  1
2012 Snyder SA, Thomas SB, Mayer AC, Breazzano SP. Total syntheses of hopeanol and hopeahainol A empowered by a chiral Brønsted acid induced pinacol rearrangement. Angewandte Chemie (International Ed. in English). 51: 4080-4. PMID 22431237 DOI: 10.1002/anie.201107730  1
2012 Snyder SA, Treitler DS. Synthesis of Et2SBr•SbCl5Br and its use in biomimetic brominative polyene cyclizations Organic Syntheses. 88: 54-69. DOI: 10.15227/orgsyn.088.0054  1
2012 Xu LM, Liang YF, Ye QD, Yang Z, Foley M, Snyder SA, Ma DW. Diversity-Oriented Syntheses of Natural Products and Natural Product-Like Compounds Organic Chemistry - Breakthroughs and Perspectives. 1-31. DOI: 10.1002/9783527664801.ch1  1
2012 Snyder SA. Strategies for the Controlled Synthesis of Oligomeric Polyphenols Recent Advances in Polyphenol Research, Volume 3. 3: 311-351. DOI: 10.1002/9781118299753.ch13  1
2011 Snyder SA, Brill ZG. Structural revision and total synthesis of caraphenol B and C. Organic Letters. 13: 5524-7. PMID 21942557 DOI: 10.1021/ol2022406  1
2011 Snyder SA, Treitler DS, Brucks AP, Sattler W. A general strategy for the stereocontrolled preparation of diverse 8- and 9-membered Laurencia-type bromoethers. Journal of the American Chemical Society. 133: 15898-901. PMID 21919540 DOI: 10.1021/ja2069449  1
2011 Snyder SA, Wright NE, Pflueger JJ, Breazzano SP. Total syntheses of heimiol A, hopeahainol D, and constrained analogues. Angewandte Chemie (International Ed. in English). 50: 8629-33. PMID 21793142 DOI: 10.1002/anie.201103575  1
2011 Snyder SA, Gollner A, Chiriac MI. Regioselective reactions for programmable resveratrol oligomer synthesis. Nature. 474: 461-6. PMID 21697944 DOI: 10.1038/nature10197  1
2011 Snyder SA. Natural product synthesis: making nematodes nervous. Nature Chemistry. 3: 422-3. PMID 21602850 DOI: 10.1038/nchem.1059  1
2011 Snyder SA, Wespe DA, von Hof JM. A concise, stereocontrolled total synthesis of rippertenol. Journal of the American Chemical Society. 133: 8850-3. PMID 21574654 DOI: 10.1021/ja202859f  1
2011 Snyder SA, ElSohly AM, Kontes F. Synthetic approaches to oligomeric natural products. Natural Product Reports. 28: 897-924. PMID 21412558 DOI: 10.1039/c1np00001b  1
2011 Snyder SA, Kontes F, ElSohly AM. Mechanistic investigations of the cyclocondensation step of the knorr pyrrole synthesis Heterocycles. 84: 265-274. DOI: 10.3987/COM-11-S(P)5  1
2011 Snyder SA, Kontes F. Synthetic studies of biomimetic Diels-Alder processes toward the helicterin family of natural products Israel Journal of Chemistry. 51: 378-390. DOI: 10.1002/ijch.201100004  1
2011 Snyder SA. Synthetic Approaches to the Resveratrol-Based Family of Oligomeric Natural Products Biomimetic Organic Synthesis. 2: 695-721. DOI: 10.1002/9783527634606.ch19  1
2011 Snyder SA, Treitler DS, Brucks AP. Halonium-induced cyclization reactions Aldrichimica Acta. 44: 27-42.  1
2010 Snyder SA, Elsohly AM, Kontes F. Synthetic and theoretical investigations of myrmicarin biosynthesis. Angewandte Chemie (International Ed. in English). 49: 9693-8. PMID 21069649 DOI: 10.1002/anie.201005825  1
2010 Snyder SA, Treitler DS, Brucks AP. Simple reagents for direct halonium-induced polyene cyclizations. Journal of the American Chemical Society. 132: 14303-14. PMID 20858010 DOI: 10.1021/ja106813s  1
2010 Snyder SA, Sherwood TC, Ross AG. Total syntheses of dalesconol A and B. Angewandte Chemie (International Ed. in English). 49: 5146-50. PMID 20572237 DOI: 10.1002/anie.201002264  1
2010 Snyder SA. Organic chemistry: Symmetrizing the unsymmetrical. Nature. 465: 560-1. PMID 20520702 DOI: 10.1038/465560a  1
2010 Welsch ME, Snyder SA, Stockwell BR. Privileged scaffolds for library design and drug discovery. Current Opinion in Chemical Biology. 14: 347-61. PMID 20303320 DOI: 10.1016/j.cbpa.2010.02.018  1
2010 Snyder SA, Treitler DS, Schall A. A two-step mimic for direct, asymmetric bromonium- and chloronium-induced polyene cyclizations Tetrahedron. 66: 4796-4804. DOI: 10.1016/j.tet.2010.03.037  1
2009 Snyder SA, Treitler DS. Et2SBrSbCl5Br: an effective reagent for direct bromonium-induced polyene cyclizations. Angewandte Chemie (International Ed. in English). 48: 7899-903. PMID 19757473 DOI: 10.1002/anie.200903834  1
2009 Pors K, Goldberg FW, Leamon CP, Rigby AC, Snyder SA, Falconer RA. The changing landscape of cancer drug discovery: a challenge to the medicinal chemist of tomorrow. Drug Discovery Today. 14: 1045-50. PMID 19638319 DOI: 10.1016/j.drudis.2009.07.004  1
2009 Snyder SA, Tang ZY, Gupta R. Enantioselective total synthesis of (-)-napyradiomycin A1 via asymmetric chlorination of an isolated olefin. Journal of the American Chemical Society. 131: 5744-5. PMID 19338329 DOI: 10.1021/ja9014716  1
2009 Snyder SA, 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. 131: 1745-52. PMID 19191699 DOI: 10.1021/ja806865u  1
2009 Snyder SA, Breazzano SP, Ross AG, Lin Y, Zografos AL. Total synthesis of diverse carbogenic complexity within the resveratrol class from a common building block. Journal of the American Chemical Society. 131: 1753-65. PMID 19143488 DOI: 10.1021/ja806183r  1
2009 Park N, Vanderford BJ, Snyder SA, Sarp S, Kim SD, Cho J. Effective controls of micropollutants included in wastewater effluent using constructed wetlands under anoxic condition Ecological Engineering. 35: 418-423. DOI: 10.1016/j.ecoleng.2008.10.004  0.52
2007 Snyder SA, Zografos AL, Lin Y. Total synthesis of resveratrol-based natural products: a chemoselective solution. Angewandte Chemie (International Ed. in English). 46: 8186-91. PMID 17890663 DOI: 10.1002/anie.200703333  1
2006 Snyder SA, Corey EJ. Concise total syntheses of palominol, dolabellatrienone, beta-araneosene, and isoedunol via an enantioselective Diels-Alder macrobicyclization. Journal of the American Chemical Society. 128: 740-2. PMID 16417362 DOI: 10.1021/ja0576379  1
2006 Snyder SA, Corey EJ. Regioselective aldol condensations of a cholestanone-derived dialdehyde: New twists on a classic reaction Tetrahedron Letters. 47: 2083-2086. DOI: 10.1016/j.tetlet.2006.01.136  1
2006 Snyder SA. From abyssomicin to zaragozic acid: Chemical synthesis and drug innovation Angewandte Chemie - International Edition. 45: 4714. DOI: 10.1002/anie.200602427  1
2005 Nicolaou KC, Snyder SA. Chasing molecules that were never there: misassigned natural products and the role of chemical synthesis in modern structure elucidation. Angewandte Chemie (International Ed. in English). 44: 1012-44. PMID 15688428 DOI: 10.1002/anie.200460864  1
2004 Nicolaou KC, Snyder SA, Longbottom DA, Nalbandian AZ, Huang X. New uses for the Burgess reagent in chemical synthesis: methods for the facile and stereoselective formation of sulfamidates, glycosylamines, and sulfamides. Chemistry (Weinheim An Der Bergstrasse, Germany). 10: 5581-606. PMID 15470695 DOI: 10.1002/chem.200400503  1
2004 Nicolaou KC, Hao J, Reddy MV, Rao PB, Rassias G, Snyder SA, Huang X, Chen DY, Brenzovich WE, Giuseppone N, O'Brate A, Giannakakou P. Chemistry and biology of diazonamide A: second total synthesis and biological investigations. Journal of the American Chemical Society. 126: 12897-906. PMID 15469287 DOI: 10.1021/ja040093a  1
2004 Nicolaou KC, Chen DY, Huang X, Ling T, Bella M, Snyder SA. Chemistry and biology of diazonamide A: first total synthesis and confirmation of the true structure. Journal of the American Chemical Society. 126: 12888-96. PMID 15469286 DOI: 10.1021/ja040092i  1
2004 Nicolaou KC, Snyder SA, Giuseppone N, Huang X, Bella M, Reddy MV, Rao PB, Koumbis AE, O'Brate A, Giannakakou P. 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. 126: 10174-82. PMID 15303893 DOI: 10.1021/ja040091q  1
2004 Nicolaou KC, Snyder SA, Huang X, Simonsen KB, Koumbis AE, Bigot A. Studies toward diazonamide A: initial synthetic forays directed toward the originally proposed structure. Journal of the American Chemical Society. 126: 10162-73. PMID 15303892 DOI: 10.1021/ja040090y  1
2004 Nicolaou KC, Snyder SA. The essence of total synthesis. Proceedings of the National Academy of Sciences of the United States of America. 101: 11929-36. PMID 15302925 DOI: 10.1073/pnas.0403799101  1
2004 Nicolaou KC, Snyder SA, Nalbandian AZ, Longbottom DA. A new method for the stereoselective synthesis of alpha- and beta-glycosylamines using the Burgess reagent. Journal of the American Chemical Society. 126: 6234-5. PMID 15149212 DOI: 10.1021/ja049293c  1
2003 Nicolaou KC, Bheema Rao P, Hao J, Reddy MV, Rassias G, Huang X, Chen DY, Snyder SA. The second total synthesis of diazonamide A. Angewandte Chemie (International Ed. in English). 42: 1753-8. PMID 12707898 DOI: 10.1002/anie.200351112  1
2003 Nicolaou KC, Montagnon T, Snyder SA. Tandem reactions, cascade sequences, and biomimetic strategies in total synthesis. Chemical Communications (Cambridge, England). 551-64. PMID 12669826  1
2003 Nicolaou KC, Snyder SA. Cascade reactions in total synthesis: Recent advances Actualite Chimique. 83-88.  1
2002 Nicolaou KC, Snyder SA, Montagnon T, Vassilikogiannakis G. The Diels--Alder reaction in total synthesis. Angewandte Chemie (International Ed. in English). 41: 1668-98. PMID 19750686 DOI: 10.1002/1521-3773(20020517)41:10<1668::AID-ANIE1668>3.0.CO;2-Z  1
2002 Nicolaou KC, Huang X, Snyder SA, Bheema Rao P, Bella M, Reddy MV. A novel regio- and stereoselective synthesis of sulfamidates from 1,2-diols using Burgess and related reagents: a facile entry into beta-amino alcohols. Angewandte Chemie (International Ed. in English). 41: 834-8. PMID 12491352 DOI: 10.1002/1521-3773(20020301)41:5<834::AID-ANIE834>3.0.CO;2-V  1
2002 Nicolaou KC, Longbottom DA, Snyder SA, Nalbanadian AZ, Huang X. A new method for the synthesis of nonsymmetrical sulfamides using burgess-type reagents. Angewandte Chemie (International Ed. in English). 41: 3866-70. PMID 12386873 DOI: 10.1002/1521-3773(20021018)41:20<3866::AID-ANIE3866>3.0.CO;2-T  1
2002 Nicolaou KC, Bella M, Chen DY, Huang X, Ling T, Snyder SA. Total synthesis of diazonamide A. Angewandte Chemie (International Ed. in English). 41: 3495-9. PMID 12298077 DOI: 10.1002/1521-3773(20020916)41:18<3495::AID-ANIE3495>3.0.CO;2-7  1
2001 Nicolaou KC, Huang X, Giuseppone N, Bheema Rao P, Bella M, Reddy MV, Snyder SA. Construction of the Complete Aromatic Core of Diazonamide A by a Novel Hetero Pinacol Macrocyclization Cascade Reaction We thank Drs. D. H. Huang and G. Suizdak for NMR spectroscopic and mass spectrometric assistance, respectively. Financial support for this work was provided by The Skaggs Institute for Chemical Biology, the National Institutes of Health (USA), American Biosciences, a predoctoral fellowship from the National Science Foundation (S.A.S.), a postdoctoral fellowship from the Association pour la Recherche sur le Cancer (N.G.), and grants from Abbott, Amgen, Array Biopharma, Boehringer-Ingelheim, Glaxo, Hoffmann-LaRoche, DuPont, Merck, Novartis, Pfizer, and Schering Plough. Angewandte Chemie (International Ed. in English). 40: 4705-4709. PMID 12404390 DOI: 10.1002/1521-3773(20011217)40:24<4705::AID-ANIE4705>3.0.CO;2-D  1
2000 Snyder EM, Snyder SA, Giesy JP, Blonde SA, Hurlburt GK, Summer CL, Mitchell RR, Bush DM. SCRAM: A scoring and ranking system for persistent, bioaccumulative, and toxic substances for the North American Great Lakes. Part II: Bioaccumulation potential and persistence. Environmental Science and Pollution Research International. 7: 116-21. PMID 19009433 DOI: 10.1065/espr199910.010  0.52
2000 Nicolaou KC, Snyder SA, Simonsen KB, Koumbis AE. Model Studies towards Diazonamide A: Synthesis of the Heterocyclic Core We thank Dr. D. H. Huang, Dr. G. Suizdak, and Dr. R. Chadha for NMR spectroscopic, mass spectrometric, and X-ray crystallographic assistance, respectively. We also thank Professor R. H. Grubbs for a generous gift of catalyst 30. Financial support for this work was provided by The Skaggs Institute for Chemical Biology, the National Institutes of Health (USA), a predoctoral fellowship from the National Science Foundation (S.A.S.), postdoctoral fellowships from the Alfred Benzons Foundation and the Danish Natural Science Research Council (K.B.S.), and grants from Abbott, Amgen, ArrayBiopharma, Boehringer-Ingelheim, GlaxoWellcome, Hoffmann-LaRoche, DuPont, Merck, Novartis, Pfizer, and Schering Plough. Angewandte Chemie (International Ed. in English). 39: 3473-3478. PMID 11091394 DOI: 10.1002/1521-3773(20001002)39:19<3473::AID-ANIE3473>3.0.CO;2-E  1
2000 Nicolaou KC, Koumbis AE, Snyder SA, Simonsen KB. Novel Reactions Initiated by Titanocene Methylidenes: Deoxygenation of Sulfoxides, N-Oxides, and Selenoxides We thank Drs. D. H. Huang and G. Suizdak for NMR spectroscopic and mass spectroscopic assistance, respectively. Financial support for this work was provided by The Skaggs Institute for Chemical Biology, the National Institutes of Health (USA), fellowships from the National Science Foundation (S.A.S.) and the Alfred Benzons Foundation (K.B.S.), and grants from Abbott, Amgen, Boehringer-Ingelheim, GlaxoWellcome, Hoffmann-LaRoche, DuPont, Merck, Novartis, Pfizer, and Schering Plough. Angewandte Chemie (International Ed. in English). 39: 2529-2533. PMID 10941126 DOI: 10.1002/1521-3773(20000717)39:14<2529::AID-ANIE2529>3.0.CO;2-E  1
2000 Nicolaou KC, Snyder SA, Bigot A, Pfefferkorn JA. Solution and Solid-Phase Synthesis of Functionalized 3-Arylbenzofurans by a Novel Cyclofragmentation - Release Pathway Financial support for this work was provided by The Skaggs Institute for Chemical Biology, the National Institutes of Health (USA), doctoral fellowships from the National Science Foundation (S.A.S.) and the Department of Defense (J.A.P.), and grants from Abbott, Amgen, Boehringer - Ingelheim, Glaxo, Hoffmann - La Roche, DuPont, Merck, Novartis, Pfizer, and Schering Plough. Angewandte Chemie (International Ed. in English). 39: 1093-1096. PMID 10760931 DOI: 10.1002/(SICI)1521-3773(20000317)39:6<1093::AID-ANIE1093>3.0.CO;2-S  1
2000 Markgraf JH, Sangani PK, Manalansan RJ, Snyder SA, Thummel RP. Strained heterocyclic systems. Part 21. The Menschutkin reaction Journal of Chemical Research - Part S. 561-563.  1
2000 Snyder SA, Vosburg DA, Jarvis MG, Markgraf JH. Intramolecular hetero Diels-Alder routes to γ-carboline alkaloids Tetrahedron. 56: 5329-5335.  1
1998 Markgraf JH, Snyder SA, Vosburg DA. A concise route to isocanthin-6-one Tetrahedron Letters. 39: 1111-1112. DOI: 10.1016/S0040-4039(97)10794-8  1
Show low-probability matches.