Stereoconvergent preparation of chiral vinylsilanes by cuprate substitution of α-acetoxyallylsilanes. Application to the synthesis of ( S )-(+)-bishomomanicone-Reference-Cited by-同舟云学术

Stereoconvergent preparation of chiral vinylsilanes by cuprate substitution of α-acetoxyallylsilanes. Application to the synthesis of ( S )-(+)-bishomomanicone

Published:2003-09 Issue:38 Volume:59 Page:7527-7533
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Guintchin Boris,Bienz Stefan

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference26 articles.

1. Synthesis and Rearrangement of Silylated Oxy- Cope Systems

2. Chiral Acylsilanes in Organic Synthesis. Part 3. Silicon-directed stereoselective preparation andIreland ester-enolate rearrangement ofO-acyl-substituted ?-silylated allyl alcohols

3. A Novel Stereoselective Reaction Cascade Leading fromα-Silylated Allylic Alcohols to Aldol-Type Products

4. Stereoselective preparation of 2-silylated 1,3-diols and the regioselectivity of their Peterson olefination

5. Synthesis of 4(benzyloxymethyl)(tert.-butyl)methylsilyloxy-1,2,3-pentatriene via Brook rearrangement

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