DSpace logo

Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/3311
Title: Garratt-Braverman Cyclization: a Powerful Tool for C-C Bond Format
Authors: Addy, Partha Sarathi
Keywords: Chemistry
Garratt–Braverman Cyclization
Issue Date: Aug-2012
Publisher: Thieme
Abstract: Development of new strategies for C–C bond formation remains in the forefront of organic synthesis. The base-mediated rearrangement of bis-propargyl sulfones via bis-allenes generated in situ, now known as the Garratt–Braverman cyclization (GBC), leads to the formation of two new C–C bonds. The reaction has recently drawn attention from organic chemists due to the wide scope as well as interesting mechanism. This report aims to give an account of the developments in this area with particular emphasis on synthetic applications.
URI: https://www.thieme-connect.de/products/ejournals/abstract/10.1055/s-0032-1317321
http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3311
Appears in Collections:Department of Chemistry

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.