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Scott A. Snyder - Publications

Affiliations: 
2006-2013 Chemistry Columbia University, New York, NY 
 2013-2015 Chemistry Scripps Research Institute 
 2015- Chemistry University of Chicago, Chicago, IL 
Area:
total synthesis of natural products
Website:
http://snyder-group.uchicago.edu/
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118 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
2021 Norton J, Shi S, Salahi F, Vibbert HB, Rahman M, Snyder SA. Generation of α-Boryl Radicals By H• Transfer and their Use in Cycloisomerizations. Angewandte Chemie (International Ed. in English). PMID 34405506 DOI: 10.1002/anie.202107665  0.773
2021 Qu P, Snyder SA. Concise and Stereoselective Total Syntheses of Annotinolides C, D, and E. Journal of the American Chemical Society. PMID 34338524 DOI: 10.1021/jacs.1c05942  0.305
2021 Gu Y, Norton JR, Salahi F, Lisnyak VG, Zhou Z, Snyder SA. Highly Selective Hydrogenation of C═C Bonds Catalyzed by a Rhodium Hydride. Journal of the American Chemical Society. 143: 9657-9663. PMID 34142805 DOI: 10.1021/jacs.1c04683  0.77
2021 Lynch-Colameta T, Greta S, Snyder SA. Synthesis of aza-quaternary centers Pictet-Spengler reactions of ketonitrones. Chemical Science. 12: 6181-6187. PMID 33996016 DOI: 10.1039/d1sc00882j  0.388
2021 Lisnyak VG, Sherwood TC, Snyder SA. The Development of Reaction Cascades to Synthesize Dimeric Coccinellid Alkaloids. Accounts of Chemical Research. PMID 33646762 DOI: 10.1021/acs.accounts.0c00806  0.394
2021 Zhang YA, Milkovits A, Agarawal V, Taylor CA, Snyder SA. Total Synthesis of the Meroterpenoid Manginoid A as Fueled by a Challenging Pinacol Coupling and Bicycle-forming Etherification. Angewandte Chemie (International Ed. in English). PMID 33644941 DOI: 10.1002/anie.202016178  0.387
2020 Taylor CA, Zhang YA, Snyder SA. The enantioselective total synthesis of laurendecumallene B. Chemical Science. 11: 3036-3041. PMID 34122807 DOI: 10.1039/c9sc06116a  0.325
2020 Chi HM, Cole CJF, Hu P, Taylor CA, Snyder SA. Total syntheses of spiroviolene and spirograterpene A: a structural reassignment with biosynthetic implications. Chemical Science. 11: 10939-10944. PMID 34094343 DOI: 10.1039/d0sc04686h  0.754
2020 Lisnyak VG, Snyder SA. A Concise, Enantiospecific Total Synthesis of Chilocorine C Fueled by a Reductive Cyclization/Mannich Reaction Cascade. Journal of the American Chemical Society. PMID 32551575 DOI: 10.1021/Jacs.0C04914  0.456
2020 Peng C, Arya P, Zhou Z, Snyder SA. A Concise Total Synthesis of (+)-Waihoensene Guided by Quaternary Center Analysis. Angewandte Chemie (International Ed. in English). PMID 32330370 DOI: 10.1002/Anie.202004177  0.455
2020 Chi HM, Cole CJF, Hu P, Taylor CA, Snyder SA. Total syntheses of spiroviolene and spirograterpene A: a structural reassignment with biosynthetic implications Chemical Science. 11: 10939-10944. DOI: 10.1039/D0SC04686H  0.742
2020 Taylor CA, Zhang Y, Snyder SA. The enantioselective total synthesis of laurendecumallene B Chemical Science. 11: 3036-3041. DOI: 10.1039/C9Sc06116A  0.431
2020 Cole CJF, Fuentes L, Snyder SA. Asymmetric pyrone Diels–Alder reactions enabled by dienamine catalysis Chemical Science. 11: 2175-2180. DOI: 10.1039/C9Sc05738B  0.357
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  0.326
2019 Ozog S, Timberlake ND, Hermann K, Garijo O, Haworth KG, Shi G, Glinkerman CM, Schefter LE, D'Souza S, Simpson E, Sghia-Hughes G, Carillo RR, Boger DL, Kiem HP, Slukvin I, ... ... Snyder SA, et al. Resveratrol trimer enhances gene delivery to hematopoietic stem cells by reducing antiviral restriction at endosomes. Blood. PMID 31416800 DOI: 10.1182/Blood.2019000040  0.385
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  0.776
2019 Zhou Z, Gao AX, Snyder SA. The Total Synthesis of (+)-Arborisidine. Journal of the American Chemical Society. PMID 31017434 DOI: 10.1021/Jacs.9B03248  0.468
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  0.443
2019 Yang M, Yin F, Fujino H, Snyder SA. The Total Synthesis of Chalcitrin. Journal of the American Chemical Society. PMID 30813728 DOI: 10.1021/Jacs.8B12612  0.458
2019 Eagan JM, Kanyiva KS, Hori M, Snyder SA. Total synthesis, reactivity, and structural clarification of lindenatriene Tetrahedron. 75: 3145-3153. DOI: 10.1016/J.Tet.2019.04.051  0.786
2018 Lisnyak VG, Lynch-Colameta T, Snyder SA. Mannich-type Reactions of Cyclic Nitrones: Effective Methods for the Enantioselective Synthesis of Piperidine-containing Alkaloids. Angewandte Chemie (International Ed. in English). PMID 30276949 DOI: 10.1002/Anie.201809799  0.465
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  0.448
2018 Snyder S, Cole C, Chi H, DeBacker K. Synthesis of Enhanced, Isolable Disulfanium Salts and their Application to Thiiranium-Promoted Polyene Cyclizations Synthesis. 50: 4351-4358. DOI: 10.1055/S-0037-1609754  0.793
2017 Snyder SA. Strategies and Tactics for the Synthesis of Complex Alkaloids. Chimia. 71: 802-809. PMID 29289241 DOI: 10.2533/Chimia.2017.802  0.475
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  0.348
2017 Schevenels FT, Shen M, Snyder SA. Isolable and Readily Handled Halophosphonium Pre-reagents for Hydro- and Deuteriohalogenation. Journal of the American Chemical Society. PMID 28462991 DOI: 10.1021/Jacs.6B12653  0.352
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  0.348
2017 Smith MW, Zhou Z, Gao AX, Shimbayashi T, Snyder SA. A 7-Step Formal Asymmetric Total Synthesis of Strictamine via an Asymmetric Propargylation and Metal-Mediated Cyclization. Organic Letters. 19: 1004-1007. PMID 28253628 DOI: 10.1021/Acs.Orglett.6B03839  0.465
2016 Schevenels FT, Shen M, Snyder SA. Alkyldisulfanium Salts: Isolable, Electrophilic Sulfur Reagents Competent for Polyene Cyclizations. Organic Letters. PMID 27973855 DOI: 10.1021/Acs.Orglett.6B02059  0.391
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  0.418
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  0.452
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  0.456
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  0.826
2015 Jepsen TH, Thomas SB, Lin Y, Stathakis CI, de Miguel I, Snyder SA. ChemInform Abstract: Harnessing Quinone Methides: Total Synthesis of (.+-.)-Vaticanol A. Cheminform. 46. DOI: 10.1002/chin.201501215  0.772
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  0.761
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  0.457
2014 Snyder SA, Berova N. Asymmetric alkene halogenation. Chirality. 26: 327. PMID 24946765 DOI: 10.1002/Chir.22345  0.379
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  0.771
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  0.481
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  0.629
2014 Carreira EM, Krautwald S, Wright NE, Snyder SA. Total Synthesis of Caraphenol A Synfacts. 10: 448-448. DOI: 10.1055/S-0033-1341099  0.451
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  0.402
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  0.356
2014 Snyder SA. Design and Strategy in Organic Synthesis. From the Chiron Approach to Catalysis. By Stephen Hanessian, Simon Giroux and Bradley Merner. Angewandte Chemie International Edition. 53: 3547-3547. DOI: 10.1002/Anie.201310098  0.338
2014 Snyder SA. Design and Strategy in Organic Synthesis. From the Chiron Approach to Catalysis. Herausgegeben von Stephen Hanessian, Simon Giroux und Bradley Merner. Angewandte Chemie. 126: 3617-3617. DOI: 10.1002/Ange.201310098  0.339
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  0.462
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  0.748
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  0.752
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  0.79
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  0.775
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  0.465
2012 Yu J, Meijer EW, Booker SJ, Mapp AK, Jamison TF, Aube J, Wasielewski MR, Schuster DI, Snyder SA, Tang Y, Chang CJ, Glorius F, Feringa B. Arthur C. Cope Scholar Awards and Eli Lilly Award Angewandte Chemie. 51: 8693-8694. DOI: 10.1002/Anie.201204828  0.437
2012 Snyder SA, Treitler DS. Synthesis of Et2SBr•SbCl5Br and its use in biomimetic brominative polyene cyclizations Organic Syntheses. 88: 54-69. DOI: 10.1002/0471264229.Os088.06  0.808
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  0.372
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  0.786
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  0.328
2011 Snyder SA, Gollner A, Chiriac MI. Regioselective reactions for programmable resveratrol oligomer synthesis. Nature. 474: 461-6. PMID 21697944 DOI: 10.1038/Nature10197  0.418
2011 Snyder SA. Natural product synthesis: making nematodes nervous. Nature Chemistry. 3: 422-3. PMID 21602850 DOI: 10.1038/Nchem.1059  0.378
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  0.803
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  0.772
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  0.801
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  0.792
2011 Snyder SA. Heterocycles in Natural Product Synthesis. Edited by Krishna C. Majumdar and Shital K. Chattopadhyay. Angewandte Chemie International Edition. 51: 1307-1307. DOI: 10.1002/Anie.201107991  0.349
2011 Snyder SA. Heterocycles in Natural Product Synthesis. Herausgegeben von Krishna C. Majumdar und Shital K. Chattopadhyay. Angewandte Chemie. 124: 1333-1333. DOI: 10.1002/Ange.201107991  0.35
2011 Snyder SA, Treitler DS, Brucks AP. Halonium-induced cyclization reactions Aldrichimica Acta. 44: 27-42.  0.754
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  0.756
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  0.818
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  0.428
2010 Snyder SA. Organic chemistry: Symmetrizing the unsymmetrical. Nature. 465: 560-1. PMID 20520702 DOI: 10.1038/465560A  0.315
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  0.344
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  0.814
2010 Nicolaou KC, Snyder SA, Montagnon T, Vassilikogiannakis G. ChemInform Abstract: The Diels-Alder Reaction in Total Synthesis Cheminform. 33: no-no. DOI: 10.1002/chin.200236259  0.568
2010 Nicolaou KC, Huang X, Snyder SA, Rao PB, Bella M, Reddy MV. ChemInform Abstract: A Novel Regio- and Stereoselective Synthesis of Sulfamidates from 1,2-Diols Using Burgess and Related Reagents: A Facile Entry into β-Amino Alcohols. Cheminform. 33: no-no. DOI: 10.1002/chin.200231088  0.482
2010 Nicolaou KC, Huang X, Giuseppone N, Rao PB, Bella M, Reddy MV, Snyder SA. ChemInform Abstract: Construction of the Complete Aromatic Core of Diazonamide A by a Novel Hetero Pinacol Macrocyclization Cascade Reaction. Cheminform. 33: no-no. DOI: 10.1002/chin.200218158  0.698
2010 Nicolaou KC, Snyder SA, Bigot A, Pfefferkorn JA. ChemInform Abstract: Solution and Solid-Phase Synthesis of Functionalized 3-Arylbenzofurans by a Novel Cyclofragmentation-Release Pathway. Cheminform. 31: no-no. DOI: 10.1002/chin.200021111  0.465
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  0.759
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  0.362
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  0.815
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  0.809
2009 Snyder SA. Book review: Classics in Stereoselective Synthesis Chirality. 22: 542-542. DOI: 10.1002/Chir.20762  0.386
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  0.795
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  0.647
2006 Corey E, Snyder S. Synthesis of Palominol and Dolabellatrienone Synfacts. 2006: 0531-0531. DOI: 10.1055/S-2006-934485  0.629
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  0.617
2006 Snyder SA. From abyssomicin to zaragozic acid: Chemical synthesis and drug innovation Angewandte Chemie - International Edition. 45: 4714. DOI: 10.1002/Anie.200602427  0.322
2006 Snyder SA. Von Abyssomicin zu Saragossasäure: chemische Synthese und Wirkstoff-Innovation Angewandte Chemie. 118: 4830-4830. DOI: 10.1002/Ange.200602427  0.322
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  0.603
2005 Nicolaou KC, Snyder SA. Die Jagd auf Moleküle, die nie existiert haben: Falsch zugeordnete Naturstoffstrukturen und die Rolle der chemischen Synthese in der modernen Strukturaufklärung Angewandte Chemie. 117: 2086-2086. DOI: 10.1002/Ange.200590046  0.478
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  0.605
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  0.754
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  0.725
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  0.776
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  0.598
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  0.583
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  0.558
2004 Nicolaou KC, Hao J, Reddy MV, Bheema Rao P, Rassias G, Snyder SA, Huang X, Chen DY, Brenzovich WE, Giuseppone N, Giannakakou P, O'Brate A. Chemistry and Biology of Diazonamide A:  Second Total Synthesis and Biological Investigations [J. Am. Chem. Soc.2004,126, 12897−12906]. Journal of the American Chemical Society. 126: 15316-15316. DOI: 10.1021/Ja0408247  0.722
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 [J. Am. Chem. Soc.2004,126, 12888−12896]. Journal of the American Chemical Society. 126: 15316-15316. DOI: 10.1021/Ja040823E  0.58
2004 Nicolaou KC, Snyder SA, Giuseppone N, Huang X, Bella M, Reddy MV, Bheema Rao P, Koumbis AE, 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 [J. Am. Chem. Soc.2004,126, 10174−10182]. Journal of the American Chemical Society. 126: 15316-15316. DOI: 10.1021/Ja040822M  0.753
2004 Nicolaou KC, Snyder SA, Nalbandian AZ, Longbottom DA. A New Method for the Stereoselective Synthesis of α- and β-Glycosylamines Using the Burgess Reagent. Cheminform. 35. DOI: 10.1002/chin.200439173  0.472
2004 Nicolaou KC, Mitchell HJ, Snyder SA. Synthesis of Complex Carbohydrates: Everninomicin 13,384-1 Cheminform. 35. DOI: 10.1002/chin.200430258  0.606
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  0.619
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 DOI: 10.1039/B209440C  0.633
2003 Nicolaou KC, Snyder SA. Cascade reactions in total synthesis: Recent advances Actualite Chimique. 83-88.  0.317
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  0.627
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  0.664
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  0.558
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  0.73
2002 Corey EJ, Nicolaou KC, Snyder SA, Montagnon T, Vassilikogiannakis G. Cover Picture: Angew. Chem. Int. Ed. 10/2002 Angewandte Chemie International Edition. 41: 1629-1629. DOI: 10.1002/1521-3773(20020517)41:10<1629::Aid-Anie1629>3.0.Co;2-0  0.667
2002 Nicolaou KC, Snyder SA, Montagnon T, Vassilikogiannakis GE. Die Diels-Alder-Reaktion in der Totalsynthese Angewandte Chemie. 114: 1742-1773. DOI: 10.1002/1521-3757(20020517)114:10<1742::Aid-Ange1742>3.0.Co;2-Y  0.484
2002 Corey EJ, Nicolaou KC, Snyder SA, Montagnon T, Vassilikogiannakis GE. Titelbild: Angew. Chem. 10/2002 Angewandte Chemie. 114: 1703-1703. DOI: 10.1002/1521-3757(20020517)114:10<1703::Aid-Ange1703>3.0.Co;2-#  0.602
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  0.737
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  0.446
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  0.505
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  0.684
2000 Snyder SA, Vosburg DA, Jarvis MG, Markgraf JH. Intramolecular hetero Diels-Alder routes to γ-carboline alkaloids Tetrahedron. 56: 5329-5335. DOI: 10.1016/S0040-4020(00)00468-3  0.445
2000 Nicolaou KC, Koumbis AE, Snyder SA, Simonsen KB. ChemInform Abstract: Novel Reactions Initiated by Titanocene Methylidenes: Deoxygenation of Sulfoxides, N-Oxides, and Selenoxides. Cheminform. 31: no-no. DOI: 10.1002/chin.200043063  0.467
2000 Nicolaou K, Snyder S, Simonsen K, Koumbis A. Model Studies towards Diazonamide A: Synthesis of the Heterocyclic Core Angewandte Chemie. 112: 3615-3620. DOI: 10.1002/1521-3757(20001002)112:19<3615::Aid-Ange3615>3.0.Co;2-K  0.581
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  0.434
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