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:	Department of Chemistry
Series:	JOURNAL OF ORGANIC CHEMISTRY, Volume 74, issue 19
ISSN:	0022-3263 1520-6904
DOI-number:	10.1021/jo9017588
» 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 . https://doi.org/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