Literature DB >> 17474778

Enantioselectively organocatalytic Michael addition of ketones to alkylidene malonates.

Chun-Li Cao1, Xiu-Li Sun, Jiao-Long Zhou, Yong Tang.   

Abstract

An organocatalytic asymmetric Michael addition of ketones to alkylidene malonates has been developed. In the presence of 20 mol % of urea 1a or N-(pyrrolidin-2-ylmethyl)trifluoromethanesulfonamide 1j, the reactions of ketones with alkylidene malonates afford the desired Michael adducts in moderate to good yields with good to high enantioselectivities under mild conditions.

Entities:  

Year:  2007        PMID: 17474778     DOI: 10.1021/jo070070p

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


  2 in total

1.  Enantioselective α-Chlorination of Aldehydes with Recyclable Fluorous (S)-Pyrrolidine-Thiourea Bifunctional Organocatalyst.

Authors:  Liang Wang; Chun Cai; Dennis P Curran; Wei Zhang
Journal:  Synlett       Date:  2010-01-01       Impact factor: 2.454

2.  Lewis acid-catalyzed conjugate additions of silyloxyallenes: a selective solution to the intermolecular Rauhut-Currier problem.

Authors:  Troy E Reynolds; Michael S Binkley; Karl A Scheidt
Journal:  Org Lett       Date:  2008-05-14       Impact factor: 6.005

  2 in total

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