A STEREOSELECTIVE SYNTHESIS OF (PLUS-OR-MINUS)-ELEMENOL VIA AN INTRAMOLECULAR SN2' ESTER ENOLATE ALKYLATION

Authors
KIM D LIM JI SHIN KJ KIM HS
Citation
D. Kim et al., A STEREOSELECTIVE SYNTHESIS OF (PLUS-OR-MINUS)-ELEMENOL VIA AN INTRAMOLECULAR SN2' ESTER ENOLATE ALKYLATION, Tetrahedron letters, 34(41), 1993, pp. 6557-6558
Citations number
16
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron letters → ACNP
ISSN journal
00404039
Volume
34
Issue
41
Year of publication
1993
Pages
6557 - 6558
Database
ISI
SICI code
0040-4039(1993)34:41<6557:ASSO(V>2.0.ZU;2-2
Abstract
The monocyclic sesquiterpene, (+/-)-elemol (1) has been synthesized in a highly stereoselective manner by an intramolecular S(N)2' ester eno late alkylation route.