STEREOSELECTIVE ROUTE TO FUNCTIONALIZED CIS-HYDRINDANES FROM TRICYCLO[5.2.1.02,6]DECAN-10-ONES - A TOTAL SYNTHESIS OF (PLUS-OR-MINUS)-CORONAFACIC ACID

Authors
MEHTA G PRAVEEN M
Citation
G. Mehta et M. Praveen, STEREOSELECTIVE ROUTE TO FUNCTIONALIZED CIS-HYDRINDANES FROM TRICYCLO[5.2.1.02,6]DECAN-10-ONES - A TOTAL SYNTHESIS OF (PLUS-OR-MINUS)-CORONAFACIC ACID, Journal of the Chemical Society, Chemical Communications, (20), 1993, pp. 1573-1575
Citations number
27
Categorie Soggetti
Chemistry
Journal title
Journal of the Chemical Society, Chemical Communications → ACNP
ISSN journal
00224936
Issue
20
Year of publication
1993
Pages
1573 - 1575
Database
ISI
SICI code
0022-4936(1993):20<1573:SRTFCF>2.0.ZU;2-W
Abstract
A flexible approach to functionalized cis-hydrindanes via Haller-Bauer type cleavage of endo-tricyclo[5.2.1.02,6]decan-10-ones is delineated and its efficacy demonstrated through a concise synthesis of (+/-)-co ronafacic acid.