Literature DB >> 11672226

A Three-Step Procedure for Asymmetric Catalytic Reductive Amidation of Ketones.

Mark J. Burk1, Guy Casy, Nicholas B. Johnson.   

Abstract

Entities:  

Year:  1998        PMID: 11672226     DOI: 10.1021/jo9809332

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


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  4 in total

1.  An expedient reductive method for conversion of ketoximes to the corresponding carbonyl compounds.

Authors:  Max M Majireck; Jason A Witek; Steven M Weinreb
Journal:  Tetrahedron Lett       Date:  2010-07-01       Impact factor: 2.415

2.  Efficient synthesis of chiral beta-arylisopropylamines by using catalytic asymmetric hydrogenation.

Authors:  Jian Chen; Weicheng Zhang; Huiling Geng; Wei Li; Guohua Hou; Aiwen Lei; Xumu Zhang
Journal:  Angew Chem Int Ed Engl       Date:  2009       Impact factor: 15.336

3.  Catalytic asymmetric synthesis using feedstocks: an enantioselective route to 2-arylpropionic acids and 1-arylethyl amines via hydrovinylation of vinyl arenes.

Authors:  Craig R Smith; T V RajanBabu
Journal:  J Org Chem       Date:  2009-04-17       Impact factor: 4.354

4.  Computational study of the mechanism and selectivity of ruthenium-catalyzed hydroamidations of terminal alkynes.

Authors:  Bholanath Maity; Lukas J Gooßen; Debasis Koley
Journal:  Chem Sci       Date:  2015-02-18       Impact factor: 9.825

  4 in total

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