Total syntheses of amphidinolides B1, B4, G1, H1 and structure revision of amphidinolide H2.
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Catalytic enantioselective synthesis of chiral organic compounds of ultra-high purity of >99% eeTotal Synthesis, Stereochemical Revision, and Biological Reassessment of Mandelalide A: Chemical Mimicry of Intrafamily Relationships.Efficient synthesis of the C(7)-C(20) subunit of amphidinolides C and FToward an enantioselective synthesis of (-)-zampanolide: preparation of the C9-C20 regionStructure-Reactivity Relationships in Lithiated Evans Enolates: Influence of Aggregation and Solvation on the Stereochemistry and Mechanism of Aldol AdditionsEvans Enolates: Solution Structures of Lithiated Oxazolidinone-Derived Enolates.Amphidinolide B: total synthesis, structural investigation, and biological evaluation.Exploiting hidden symmetry in natural products: total syntheses of amphidinolides C and F.Survey of marine natural product structure revisions: a synergy of spectroscopy and chemical synthesis.Natural product analogues: towards a blueprint for analogue-focused synthesis.Molecular editing and assessment of the cytotoxic properties of iejimalide and progeny.Gram-scale synthesis of iejimalide B.Preparation, modification, and evaluation of cruentaren A and analogues.Total synthesis of the protected aglycon of fidaxomicin (tiacumicin B, lipiarmycin A3).Total synthesis, proof of absolute configuration, and biosynthetic origin of stylopsal, the first isolated sex pheromone of strepsiptera.Two Enabling Strategies for the Stereoselective Conversion of Internal Alkynes into Trisubstituted Alkenes.Gold Catalysis for Heterocyclic Chemistry: A Representative Case Study on Pyrone Natural Products.Total Synthesis of (6R,10R,13R,14R,16R,17R,19S,20R,21R,24S, 25S,28S,30S,32R,33R,34R,36S,37S,39R)-Azaspiracid-3 Reveals Non-Identity with the Natural Product.Stereochemical Definition of the Natural Product (6R,10R,13R, 14R,16R,17R,19S,20S,21R,24S,25S,28S,30S,32R,33R,34R,36S,37S,39R)-Azaspiracid-3 by Total Synthesis and Comparative Analyses.Concise total syntheses of amphidinolides C and F.Stereospecific Synthesis of Fluoroalkenes by Silver-Mediated Fluorination of Functionalized Alkenylstannanes.Concise Synthesis of a Pateamine A Analogue with In Vivo Anticancer Activity Based on an Iron-Catalyzed Pyrone Ring Opening/Cross-Coupling.Total Synthesis of Amphidinolide FChemoenzymatic One-Pot Synthesis of γ-Butyrolactones
P2860
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P2860
Total syntheses of amphidinolides B1, B4, G1, H1 and structure revision of amphidinolide H2.
description
2009 nî lūn-bûn
@nan
2009 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Total syntheses of amphidinoli ...... revision of amphidinolide H2.
@ast
Total syntheses of amphidinoli ...... revision of amphidinolide H2.
@en
type
label
Total syntheses of amphidinoli ...... revision of amphidinolide H2.
@ast
Total syntheses of amphidinoli ...... revision of amphidinolide H2.
@en
prefLabel
Total syntheses of amphidinoli ...... revision of amphidinolide H2.
@ast
Total syntheses of amphidinoli ...... revision of amphidinolide H2.
@en
P2093
P356
P1476
Total syntheses of amphidinoli ...... revision of amphidinolide H2.
@en
P2093
Daniel Laurich
Florent Beaufils
François-Hugues Porée
Jaques-Alexis Funel
Laure C Bouchez
Louis Morency
Minoru Tamiya
Ryan Gilmour
Vilnis Liepins
P304
P356
10.1002/CHEM.200802067
P407
P577
2009-01-01T00:00:00Z