Literature DB >> 12688755

Geometrically selective synthesis of functionalized beta,beta-disubstituted vinylic sulfoxides by Cu-catalyzed conjugate addition of organozinc reagents to 1-alkynyl sulfoxides.

Naoyoshi Maezaki1, Hiroaki Sawamoto, Ryoko Yoshigami, Tomoko Suzuki, Tetsuaki Tanaka.   

Abstract

[reaction: see text] A new synthetic method of chiral beta,beta-disubstituted vinylic sulfoxides bearing various functionalities has been developed by employing Cu-catalyzed conjugate addition of an organozinc reagent to chiral 1-alkynyl sulfoxide. Since the reaction proceeds with very high syn-selectivity, both geometric beta,beta-disubstituted vinylic sulfoxides were stereoselectively synthesized by changing the combination of 1-alkynyl sulfoxide and the organozinc reagent.

Entities:  

Year:  2003        PMID: 12688755     DOI: 10.1021/ol034289b

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  2 in total

1.  Recent advances in carbocupration of α-heterosubstituted alkynes.

Authors:  Ahmad Basheer; Ilan Marek
Journal:  Beilstein J Org Chem       Date:  2010-07-15       Impact factor: 2.883

2.  Recent advances in transition-metal-catalyzed intermolecular carbomagnesiation and carbozincation.

Authors:  Kei Murakami; Hideki Yorimitsu
Journal:  Beilstein J Org Chem       Date:  2013-02-11       Impact factor: 2.883

  2 in total

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