A METHODOLOGY FOR SPIROCYCLOPENTANNULATION - STEREOSELECTIVE TOTAL SYNTHESIS OF (+ -)-TOCHUINYL ACETATE AND (+/-)-DIHYDROTOCHUINYL ACETATE/

Authors
SRIKRISHNA A REDDY TJ KUMAR PP VIJAYKUMAR D
Citation
A. Srikrishna et al., A METHODOLOGY FOR SPIROCYCLOPENTANNULATION - STEREOSELECTIVE TOTAL SYNTHESIS OF (+ -)-TOCHUINYL ACETATE AND (+/-)-DIHYDROTOCHUINYL ACETATE/, Synlett, (1), 1996, pp. 67
Citations number
13
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Synlett → ACNP
ISSN journal
09365214
Issue
1
Year of publication
1996
Database
ISI
SICI code
0936-5214(1996):1<67:AMFS-S>2.0.ZU;2-H
Abstract
A methodology based on Claisen rearrangement and Wacker oxidation for the spirocyclopentannulation of ketones, and its application to a high ly stereoselective first total synthesis of dihydrotochuinyl acetate ( (8) under bar) is described.