Asymmetrized trils (hydroxymethyl)methane as a highly stereodivergent chiral building block: preparation of all four stereoisomers of protected 2-hydroxymethyl-1,3-butanediol-Reference-Cited by-同舟云学术

Asymmetrized trils (hydroxymethyl)methane as a highly stereodivergent chiral building block: preparation of all four stereoisomers of protected 2-hydroxymethyl-1,3-butanediol

Published:1990-01 Issue:44 Volume:31 Page:6421-6424
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Guanti Giuseppe,Banfi Luca,Narisano Enrica

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference17 articles.

1. Double Asymmetric Synthesis and a New Strategy for Stereochemical Control in Organic Synthesis

2. Enzymes as selective reagents in organic synthesis: Enantioselective preparation of “asymmetrized tris (hydroxymethyl)methane”

3. Guanti G., Banff L., and Narisano E., Tetrahedron: Asymmetry, in press.

4. Enantiodivergent syntheses of (+)- and (-)-nonactic acid and the total synthesis of nonactin

5. A short, stereodivergent synthesis of the racemic erythro and threo diastereomers of 6-acetoxy-5-hexadecanolide, a mosquito oviposition attractant pheromone

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