Literature DB >> 26991132

A General and Selective Rhodium-Catalyzed Reduction of Amides, N-Acyl Amino Esters, and Dipeptides Using Phenylsilane.

Shoubhik Das1, Yuehui Li1, Liang-Qiu Lu1, Kathrin Junge1, Matthias Beller2.   

Abstract

This article describes a selective reduction of functionalized amides, including N-acyl amino esters and dipeptides, to the corresponding amines using simple [Rh(acac)(cod)]. The catalyst shows excellent chemoselectivity in the presence of different sensitive functional moieties.
© 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  amides; esters; hydrosilylation; peptides; rhodium

Mesh:

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Year:  2016        PMID: 26991132     DOI: 10.1002/chem.201600535

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  2 in total

1.  Site Selective Amide Reduction of Cyclosporine A Enables Diverse Derivation of an Important Cyclic Peptide.

Authors:  Michael T Peruzzi; Fabrice Gallou; Stephen J Lee; Michel R Gagné
Journal:  Org Lett       Date:  2019-04-17       Impact factor: 6.005

2.  A high-performance liquid chromatography-electronic circular dichroism online method for assessing the absolute enantiomeric excess and conversion ratio of asymmetric reactions.

Authors:  Xiang Zhang; Mingchao Wang; Li Li; Dali Yin
Journal:  Sci Rep       Date:  2017-03-02       Impact factor: 4.379

  2 in total

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