The ring contraction of δ-lactones with leaving group α-substituents: a strategy for the synthesis of 2,5-disubstituted highly functionalised homochiral tetrahydrofurans-Reference-Cited by-同舟云学术

The ring contraction of δ-lactones with leaving group α-substituents: a strategy for the synthesis of 2,5-disubstituted highly functionalised homochiral tetrahydrofurans

Published:1992 Issue:21 Volume: Page:1605-1607
ISSN:0022-4936
Container-title:J. Chem. Soc., Chem. Commun.
language:en
Short-container-title:J. Chem. Soc., Chem. Commun.

Author:

Choi Sik-Man S.,Myerscough Paul M.,Fairbanks Antony J.,Skead Ben M.,Bichard Claire J. F.,Mantell Simon J.,Son Jong Chan,Fleet George W. J.,Saunders John,Brown David

Publisher

Royal Society of Chemistry (RSC)

Subject

Molecular Medicine

Link

http://pubs.rsc.org/en/content/articlepdf/1992/C3/C39920001605

Reference14 articles.

1. A reductive aldol strategy for the synthesis of very highly substituted cyclopentanes from sugar lactones

2. Synthesis of, and lack of inhibition of a rhamnosidase by, both enantiomers of deoxyrhamnojirimycin and rhamnolactam: β-mannosidase inhibition by δ-lactams

3. Alexines from heptonolactones

4. (+)-Muscarine from L-rhamnose

5. 3R-Hydroxymuscarine from L-rhamnose without protection

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