TIN-PROMOTED STEREOCONTROLLED INTRAMOLECULAR ALLYLATION OF CARBONYL-COMPOUNDS - A FACILE AND STEREOSELECTIVE METHOD FOR RING CONSTRUCTION

Authors
ZHOU JY CHEN ZG WU SH
Citation
Jy. Zhou et al., TIN-PROMOTED STEREOCONTROLLED INTRAMOLECULAR ALLYLATION OF CARBONYL-COMPOUNDS - A FACILE AND STEREOSELECTIVE METHOD FOR RING CONSTRUCTION, Journal of the Chemical Society, Chemical Communications, (24), 1994, pp. 2783-2784
Citations number
14
Categorie Soggetti
Chemistry
Journal title
Journal of the Chemical Society, Chemical Communications → ACNP
ISSN journal
00224936
Issue
24
Year of publication
1994
Pages
2783 - 2784
Database
ISI
SICI code
0022-4936(1994):24<2783:TSIAOC>2.0.ZU;2-S
Abstract
The intramolecular allylation of carbonyl compounds 1 promoted by meta llic tin proceeds in a stereocontrolled manner to give cyclic products 2 with high diastereoselectivity.