Elaboration of S-(-)-α-pinene into functionalized bicyclo[4.2.1]nonane framework of mediterraneols

Mehta, Goverdhan ; Acharyulu, P. V. R. ; Reddy, K. Subba ; Umarye, Jayant D. (1997) Elaboration of S-(-)-α-pinene into functionalized bicyclo[4.2.1]nonane framework of mediterraneols Synlett, 1997 (10). pp. 1161-1162. 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-1997-985

Abstract

A two-carbon ring expansion of (-)- α -pinene 1 to bicyclo[5.1.1]nonane system (+)-12 and 1,2-cationic rearrangement provides an entry into a functionalized bicyclo[4.2.1]nonane derivative, representing the carbocyclic skeleton, present in the novel marine diterpenes, mediterraneols.

Item Type:Article
Source:Copyright of this article belongs to Thieme Medical Publishers Inc.
Keywords:"push-pull" Cyclopropane Fragmentation; Two-carbon Ring Expansion; Bicyclo[4.2. 1.]nonane; Marine Natural Products
ID Code:29157
Deposited On:18 Dec 2010 05:32
Last Modified:18 Dec 2010 05:32

Repository Staff Only: item control page