Highly Chemoselective Copper-Catalyzed Conjugate Reduction of Stereochemically Labile alpha,beta-Unsaturated Amino Ketones
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A1 Alkuperäisartikkeli tieteellisessä aikakauslehdessä
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Date
2009
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Language
en
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7598-7601
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JOURNAL OF ORGANIC CHEMISTRY, Volume 74, issue 19
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.Description
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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