Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/2638
Title: B(C6F5)3 catalysed reduction of para-quinone methides and fuchsones to access unsymmetrical diaryl- and triarylmethanes: elaboration to beclobrate
Authors: Mahesh, S.
Anand, R.V.
Keywords: Beclobrate
Triarylmethanes
para-quinone methides
B(C6F5)3
Issue Date: 2017
Publisher: Royal Society of Chemistry
Citation: Organic and Biomolecular Chemistry, 15(39), pp. 8393-8401
Abstract: A mild and efficient method for the synthesis of unsymmetrical diaryl- and triarylmethanes through a B(C6F5)3 catalyzed reduction of para-quinone methides and fuchsones respectively, using the Hantzsch ester as a reducing source has been developed. Detailed mechanistic investigations revealed that the reaction actually proceeds through a Lewis acid–base pair complex derived from B(C6F5)3 and the Hantzsch ester.
URI: https://pubs.rsc.org/en/content/articlelanding/2017/ob/c7ob02007d#!divAbstract
http://hdl.handle.net/123456789/2638
Appears in Collections:Research Articles

Files in This Item:
File Description SizeFormat 
Need to add pdf.odt7.9 kBOpenDocument TextView/Open


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