Literature DB >> 12491425

A highly enantioselective and general conjugate addition of thiols to cyclic enones with an organic catalyst.

Paul McDaid1, Yonggang Chen, Li Deng.   

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Year:  2002        PMID： 12491425     DOI： 10.1002/1521-3773(20020118)41:2<338::aid-anie338>3.0.co;2-m

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


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  5 in total

1.  Catalytic asymmetric conjugate addition of simple alkyl thiols to alpha,beta-unsaturated N-acylated oxazolidin-2-ones with bifunctional catalysts.

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3.  Enantioselective bifunctional iminophosphorane catalyzed sulfa-Michael addition of alkyl thiols to unactivated β-substituted-α,β-unsaturated esters.

Authors:  Jinchao Yang; Alistair J M Farley; Darren J Dixon
Journal:  Chem Sci       Date:  2016-09-14       Impact factor: 9.825

4.  The synthesis of chiral β-naphthyl-β-sulfanyl ketones via enantioselective sulfa-Michael reaction in the presence of a bifunctional cinchona/sulfonamide organocatalyst.

Authors:  Deniz Tözendemir; Cihangir Tanyeli
Journal:  Beilstein J Org Chem       Date:  2021-02-18       Impact factor: 2.883

5.  Highly enantioselective sulfa-Michael addition reactions using N-heterocyclic carbene as a non-covalent organocatalyst.

Authors:  Jiean Chen; Sixuan Meng; Leming Wang; Hongmei Tang; Yong Huang
Journal:  Chem Sci       Date:  2015-04-23       Impact factor: 9.825
  5 in total

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