Diels-alder reactions enhanced diastereofacial selectivity in 5.0 M LiClO4-Et2O approach to the construction of the isoindolone nucleus of cytochalasans
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference5 articles.
1. Dramatic rate accelerations of Diels-Alder reactions in 5 M lithium perchlorate-diethyl ether: the cantharidin problem reexamined
2. Cytochalasan synthesis: macrocycle formation via intramolecular Diels-Alder reactions
3. Synthesis of (3S,4S)-4-amino-3-hydroxy-6-methylheptanoic acid derivatives. Analysis of diastereomeric purity
4. Conversion of allyl alcohols to 1,3-dienes by sequential sulfenate sulfoxide [2,3]-sigmatropic rearrangement and syn-elimination
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3. From Bifunctional to Trifunctional (Tricomponent Nucleophile–Transition Metal–Lewis Acid) Catalysis: The Catalytic, Enantioselective α-Fluorination of Acid Chlorides;Journal of the American Chemical Society;2011-04-22
4. ChemInform Abstract: Diels-Alder Reactions. Enhanced Diastereofacial Selectivity in 5.0 M LiClO4-Et2O Approach to the Construction of the Isoindolone Nucleus of Cytochalasans.;ChemInform;2010-08-19
5. Molecular Basis of Cytochalasan Biosynthesis in Fungi: Gene Cluster Analysis and Evidence for the Involvement of a PKS-NRPS Hybrid Synthase by RNA Silencing;Journal of the American Chemical Society;2007-07-18
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