A new methodology for the stereoselective synthesis of 4-substituted butenolides: Asymmetric Michael addition reaction of 2-(trimethylsilyloxy)furans to oxazolidinone enoates-Reference-Cited by-同舟云学术

A new methodology for the stereoselective synthesis of 4-substituted butenolides: Asymmetric Michael addition reaction of 2-(trimethylsilyloxy)furans to oxazolidinone enoates

Published:1997-12 Issue:50 Volume:53 Page:17015-17028
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Kitajima Hiroshi,Ito Katsuji,Katsuki Tsutomu

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference56 articles.

1. Chemistry of Butenolides

2. A tactically novel alternative to acyclic stereoselection based on the concept of a replicating chiron — 1,3- and 1,4-C-Methyl substitution

3. A highly convergent and enantiospecific synthesis of acyclic subunits of ionomycin from a single chiral progenitor

4. Methodoloy for the polyene and related antibiotics - enantiospecific synthesis of chiral structural units of amphotericin B from A common progenitor: the C14–C20 and C32–C38 segments

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