Highly Chemoselective Copper-Catalyzed Conjugate Reduction of Stereochemically Labile alpha,beta-Unsaturated Amino Ketones

Altmetrics



Title:	Highly Chemoselective Copper-Catalyzed Conjugate Reduction of Stereochemically Labile alpha,beta-Unsaturated Amino Ketones
Author(s):	Pelss, Andrejs ; Kumpulainen, Esa T.T. ; Koskinen, Ari M.P.
Date:	2009
Language:	en
Pages:	7598-7601
Department:	School services, CHEM Department of Chemistry Department of Chemistry and Materials Science Organic Chemistry
Series:	JOURNAL OF ORGANIC CHEMISTRY, Volume 74, issue 19
ISSN:	0022-3263 1520-6904
DOI-number:	10.1021/jo9017588
Subject:	116 Chemical sciences
Keywords:	116 Chemical sciences
» Show full item record
This publication is imported from Aalto University Research information portal: https://research.aalto.fi > View this publication in Research information portal > View/Open full text file from Research information portal
Citation: Pelss , A , Kumpulainen , E T T & Koskinen , A M P 2009 , ' Highly Chemoselective Copper-Catalyzed Conjugate Reduction of Stereochemically Labile alpha,beta-Unsaturated Amino Ketones ' JOURNAL OF ORGANIC CHEMISTRY , vol 74 , no. 19 , pp. 7598-7601 . DOI: 10.1021/jo9017588
Abstract: Highly chemoselective conjugate reduction of chiral R,β-unsaturated amino ketones has been developed by using triisopropyl phosphite ligated copper hydride complex. The highlights of the method are wide substrate compatibility and exceptional chemoselectivity.

Permanent link to this item: http://urn.fi/URN:NBN:fi:aalto-201609234353 Email this Export to RefWorks QR Code Print BibTex Tweet