ePrints@IIScePrints@IISc Home | About | Browse | Latest Additions | Advanced Search | Contact | Help

An efficient ring-closing metathesis reaction of geminally disubstituted olefins using first generation Grubbs’ catalyst: enantiospecific synthesis of pacifigorgianes

Srikrishna, A and Dethe, Dattatraya H (2003) An efficient ring-closing metathesis reaction of geminally disubstituted olefins using first generation Grubbs’ catalyst: enantiospecific synthesis of pacifigorgianes. In: Tetrahedron Letters, 44 (42). pp. 7817-7820.

[img] PDF
An_efficient_ring.pdf
Restricted to Registered users only

Download (274Kb) | Request a copy

Abstract

An efficient ring closing metathesis reaction with first generation Grubbs’ catalyst $[PhCH=RuCl_2(PCy_3)_2]$ involving geminally disubstituted olefins has been discovered. It has been extended to the enantiospecific synthesis of pacifigorgiane sesquiterpenes.

Item Type: Journal Article
Additional Information: The Copyright belongs to Elsevier.
Department/Centre: Division of Chemical Sciences > Organic Chemistry
Date Deposited: 17 May 2006
Last Modified: 19 Sep 2010 04:26
URI: http://eprints.iisc.ernet.in/id/eprint/6714

Actions (login required)

View Item View Item