STEREOSELECTIVE ROUTE TO HIGHLY FUNCTIONALIZED D,1,2,3,4,4A,6,8A,9,10,10A-DECAHYDROPHENANTHRENES, A NEW ENTRY TO THE QUASSINOID AND FUSIDANE FRAMEWORKS

Authors
VILA AJ CRAVERO RM GONZALEZSIERRA M
Citation
Aj. Vila et al., STEREOSELECTIVE ROUTE TO HIGHLY FUNCTIONALIZED D,1,2,3,4,4A,6,8A,9,10,10A-DECAHYDROPHENANTHRENES, A NEW ENTRY TO THE QUASSINOID AND FUSIDANE FRAMEWORKS, Tetrahedron, 49(21), 1993, pp. 4511-4526
Citations number
39
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron → ACNP
ISSN journal
00404020
Volume
49
Issue
21
Year of publication
1993
Pages
4511 - 4526
Database
ISI
SICI code
0040-4020(1993)49:21<4511:SRTHFD>2.0.ZU;2-1
Abstract
A series of highly functionalized angularly substituted bicyclic and t ricyclic ketones were obtained regio- and stereoselectively by means o f the Birch reductive alkylation on the properly functionalized benzyl ic ketones.