RADICAL CYCLIZATION METHODOLOGY TO LIGNANS - SYNTHESIS OF (+ -)-ENTEROLACTONE/

Authors
SRIKRISHNA A VENKATESWARLU S DANIELDOSS S SATTIGERI JA
Citation
A. Srikrishna et al., RADICAL CYCLIZATION METHODOLOGY TO LIGNANS - SYNTHESIS OF (+ -)-ENTEROLACTONE/, Indian journal of chemistry. Sect. B: organic chemistry, including medical chemistry, 34(8), 1995, pp. 679-681
Citations number
37
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Indian journal of chemistry. Sect. B: organic chemistry, including medical chemistry → ACNP
ISSN journal
03764699
Volume
34
Issue
8
Year of publication
1995
Pages
679 - 681
Database
ISI
SICI code
0376-4699(1995)34:8<679:RCMTL->2.0.ZU;2-B
Abstract
Synthesis of enterolactone, the first lignan of human origin, starting from 3-methoxycinnamyl alcohol employing a 5-exo-trig radical cyclisa tion reaction of mixed bromoacetal as the key step is described.