about
Chemistry and biology of diazonamide A: first total synthesis and confirmation of the true structure.A strategy for complex dimer formation when biomimicry fails: total synthesis of ten coccinellid alkaloids.Harnessing quinone methides: total synthesis of (±)-vaticanol A.Regioselective reactions for programmable resveratrol oligomer synthesis.Total syntheses of dalesconol A and B.Syntheses of cyclotriveratrylene analogues and their long elusive triketone congeners.Synthesis and Applications of Hajos-Parrish Ketone Isomers.The Diels--Alder reaction in total synthesis.Synthetic approaches to oligomeric natural products.Isolable and Readily Handled Halophosphonium Pre-reagents for Hydro- and Deuteriohalogenation.Enantiospecific Total Synthesis of the Highly Strained (-)-Presilphiperfolan-8-ol via a Pd-Catalyzed Tandem Cyclization.A 7-Step Formal Asymmetric Total Synthesis of Strictamine via an Asymmetric Propargylation and Metal-Mediated Cyclization.Alkyldisulfanium Salts: Isolable, Electrophilic Sulfur Reagents Competent for Polyene Cyclizations.The Enantioselective Total Synthesis of Exochomine.Pyrone Diels-Alder Routes to Indolines and Hydroindolines: Syntheses of Gracilamine, Mesembrine, and Δ(7) -Mesembrenone.Structural revision and total synthesis of caraphenol B and C.Evaluation of HIV-1 inhibition by stereoisomers and analogues of the sesquiterpenoid hydroquinone peyssonol A.Simple reagents for direct halonium-induced polyene cyclizations.Et2SBrSbCl5Br: an effective reagent for direct bromonium-induced polyene cyclizations.A new method for the stereoselective synthesis of alpha- and beta-glycosylamines using the Burgess reagent.New uses for the Burgess reagent in chemical synthesis: methods for the facile and stereoselective formation of sulfamidates, glycosylamines, and sulfamides.Studies toward diazonamide A: initial synthetic forays directed toward the originally proposed structure.Studies toward diazonamide A: development of a hetero-pinacol macrocyclization cascade for the construction of the bis-macrocyclic framework of the originally proposed structure.Enantioselective total synthesis of (-)-napyradiomycin A1 via asymmetric chlorination of an isolated olefin.Tandem reactions, cascade sequences, and biomimetic strategies in total synthesis.Explorations into neolignan biosynthesis: concise total syntheses of helicterin B, helisorin, and helisterculin A from a common intermediate.Total synthesis of diverse carbogenic complexity within the resveratrol class from a common building block.A novel regio- and stereoselective synthesis of sulfamidates from 1,2-diols using Burgess and related reagents: a facile entry into beta-amino alcohols.Total synthesis of resveratrol-based natural products: a chemoselective solution.Total Syntheses of Scaparvins B, C, and D Enabled by a Key C-H Functionalization.Total Synthesis of the Caged Indole Alkaloid Arboridinine Enabled by aza-Prins and Metal-Mediated Cyclizations.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 ProfessSynthetic and theoretical investigations of myrmicarin biosynthesis.Explorations of caffeic acid derivatives: total syntheses of rufescenolide, yunnaneic acids C and D, and studies toward yunnaneic acids A and B.Mannich-type Reactions of Cyclic Nitrones: Effective Methods for the Enantioselective Synthesis of Piperidine-containing AlkaloidsSymmetrizing the unsymmetricalConcise total syntheses of palominol, dolabellatrienone, beta-araneosene, and isoedunol via an enantioselective Diels-Alder macrobicyclizationA concise, stereocontrolled total synthesis of rippertenolNatural product synthesis: making nematodes nervousA general strategy for the stereocontrolled preparation of diverse 8- and 9-membered Laurencia-type bromoethers
P50
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P50
description
hulumtues
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researcher
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wetenschapper
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հետազոտող
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name
Scott A Snyder
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Scott A Snyder
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Scott A Snyder
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Scott A Snyder
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Scott A Snyder
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type
label
Scott A Snyder
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Scott A Snyder
@en
Scott A Snyder
@es
Scott A Snyder
@nl
Scott A Snyder
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prefLabel
Scott A Snyder
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Scott A Snyder
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Scott A Snyder
@es
Scott A Snyder
@nl
Scott A Snyder
@sl
P106
P21
P31
P496
0000-0003-3594-8769