Literature DB >> 16888823

Highly efficient asymmetric michael addition of aldehydes to nitroalkenes catalyzed by a simple trans-4-hydroxyprolylamide.

Claudio Palomo1, Silvia Vera, Antonia Mielgo, Enrique Gómez-Bengoa.   

Abstract

Entities:  

Year:  2006        PMID： 16888823     DOI： 10.1002/anie.200602207

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN： 1433-7851            Impact factor:   15.336


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  3 in total

1.  Synthesis of Prolinal Dithioacetals as Catalysts for the Highly Stereoselective Michael Addition of Ketones and Aldehydes to beta-Nitrostyrenes.

Authors:  Tanmay Mandal; Cong-Gui Zhao
Journal:  Tetrahedron Lett       Date:  2007       Impact factor: 2.415

2.  Construction of highly enantioenriched spirocyclopentaneoxindoles containing four consecutive stereocenters via thiourea-catalyzed asymmetric Michael-Henry cascade reactions.

Authors:  Yonglei Du; Jian Li; Kerong Chen; Chenglin Wu; Yu Zhou; Hong Liu
Journal:  Beilstein J Org Chem       Date:  2017-07-07       Impact factor: 2.883

3.  Formal β-C-H Arylation of Aldehydes and Ketones by Cooperative Nickel and Photoredox Catalysis.

Authors:  Kun Liu; Armido Studer
Journal:  Angew Chem Int Ed Engl       Date:  2022-06-23       Impact factor: 16.823
  3 in total

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