A facile oxy-cope rearrangement route to functionalized bicyclo[5.3.1]undecane ring system present in taxol and vinigrol diterpenoids

Mehta, Goverdhan ; Subba Reddy, K. (1996) A facile oxy-cope rearrangement route to functionalized bicyclo[5.3.1]undecane ring system present in taxol and vinigrol diterpenoids Synlett, 1996 (7). pp. 625-627. ISSN 0936-5214

Full text not available from this repository.

Official URL: https://www.thieme-connect.com/ejournals/abstract/...

Related URL: http://dx.doi.org/10.1055/s-1996-5557

Abstract

An oxy-Cope rearrangement based protocol to bicyclo[5.3.1]undecane ring system from a readily and abundantly available bicyclo[4.4.0]decane precursor is described. Several interesting transformations leading to the formation of tricyclo[6.2.1.04,11]undecane system among others are also reported.

Item Type:Article
Source:Copyright of this article belongs to Thieme Medical Publishers Inc.
Keywords:Taxol and Vinigrol Diterpenoids; [3,3]Sigmatropic Rearrangement; Carbonyl-enereaction; Carbonyl-olefin Transannular Cyclization; Functional Group Switching
ID Code:29146
Deposited On:18 Dec 2010 05:33
Last Modified:18 Dec 2010 05:33

Repository Staff Only: item control page