Access to -2,5-disubstituted iodovinyltetrahydrofurans via the cyclization of γ-silyloxyallenes using n-iodosuccinimide
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference14 articles.
1. Stereoselectivity in the syntheses of substituted 2-(2-tetrahydrofuranyl)acrylates via intramolecular oxymercurations or oxypalladations of allenes
2. Stereoselective syntheses of the nonactate esters via intramolecular oxymercurations of allenes
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4. Synthesis of the C1′–C11′ portion of pamamycin-607 via a stereoselective oxymercuration of a gamma—silyloxyallene and a stereospecific magnesium—methanol reduction
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3. ChemInform Abstract: Access to cis-2,5-Disubstituted Iodovinyltetrahydrofurans via the Cyclization of γ-Silyloxyallenes Using N-Iodosuccinimide.;ChemInform;2010-08-21
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