Literature DB >> 22936365

Enantioselective zinc-mediated conjugate addition of terminal alkynes to enones.

Gonzalo Blay1, Luz Cardona, José R Pedro, Amparo Sanz-Marco.   

Abstract

Zinc for conjugate alkynylation: The enantioselective conjugate addition of terminal alkynes to 2-arylidene-1,3-diketones in the presence of diethylzinc and a catalytic amount of (R)-VANOL has been developed. The reaction can be applied to different aromatic and heteroaromatic alkynes and enones, giving the expected products in good yield and with enantiomeric excesses up to 91%. The products can be enantiomerically enriched up to 99% ee by crystallization (see scheme).
Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Year:  2012        PMID: 22936365     DOI: 10.1002/chem.201201765

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


  3 in total

1.  Vaulted biaryls in catalysis: A structure-activity relationship guided tour of the immanent domain of the VANOL ligand.

Authors:  Yong Guan; Zhensheng Ding; William D Wulff
Journal:  Chemistry       Date:  2013-10-02       Impact factor: 5.236

2.  Palladium-Catalyzed Enantioselective Redox-Relay Heck Alkynylation of Alkenols To Access Propargylic Stereocenters.

Authors:  Zhi-Min Chen; Christine S Nervig; Ryan J DeLuca; Matthew S Sigman
Journal:  Angew Chem Int Ed Engl       Date:  2017-05-03       Impact factor: 15.336

3.  Asymmetric synthesis of chiral β-alkynyl carbonyl and sulfonyl derivatives via sequential palladium and copper catalysis.

Authors:  Barry M Trost; James T Masters; Benjamin R Taft; Jean-Philip Lumb
Journal:  Chem Sci       Date:  2016-06-10       Impact factor: 9.825

  3 in total

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