Regioselective ring cleavage of chiral β-trichloromethyl-β-propiolactone with organoaluminum compounds for the synthesis of optically active intermediates-Reference-Cited by-同舟云学术

Regioselective ring cleavage of chiral β-trichloromethyl-β-propiolactone with organoaluminum compounds for the synthesis of optically active intermediates

Published:1998-12 Issue:52 Volume:39 Page:9735-9738
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Fujisawa Tamotsu,Ito Takatoshi,Nishiura Shin,Shimizu Makoto

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference25 articles.

1. β-Methyl-β-propiolactone;Fujisawa;Encyclopedia of Reagents for Organic Syntheses,1995

2. A novel synthetic method for optically active terpenes by the ring-opening reaction of (R)-(+)-β-methyl-β-propiolactone

3. A stereocontrolled total synthesis of optically active (R,R)-phytol

4. A SIMPLE STEREOSELECTIVE SYNTHESIS OF (lR,3R,5S)-1,3-DIMETHYL-2,9-DIOXABICYCLO[3,3,1]NONANE USING REGIOSELECTIVE RING-OPENING OF (R)-β-METHYL-β-PROPIOLACTONE

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