Literature DB >> 26007677

A detachable ester bond enables perfect Z-alkylations of olefins for the synthesis of tri- and tetrasubstituted alkenes.

Takashi Nishikata1, Kimiaki Nakamura, Yuki Inoue, Shingo Ishikawa.   

Abstract

2-Vinyl-substituted phenol and an alpha-bromoester undergo a tandem esterification-alkylation reaction in the presence of a Cu-amine catalyst system to produce benzene-fused lactone. Z-Alkylated styrene is obtained after hydrolysis of the lactone with perfect selectivity. The simple protocol developed in this work opens a new avenue in the multi-substitution chemistry of alkenes.

Entities:  

Year:  2015        PMID: 26007677     DOI: 10.1039/c5cc03474d

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  1 in total

Review 1.  Recent developments in copper-catalyzed radical alkylations of electron-rich π-systems.

Authors:  Kirk W Shimkin; Donald A Watson
Journal:  Beilstein J Org Chem       Date:  2015-11-23       Impact factor: 2.883

  1 in total

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