Literature DB >> 17047794

Domino Heck-C-H activation reaction of unsymmetrically substituted [3]cumulene.

Takumi Furuta1, Tomohiro Asakawa, Mie Iinuma, Satoshi Fujii, Kiyoshi Tanaka, Toshiyuki Kan.   

Abstract

The Heck reaction of an unsymmetrically substituted [3]cumulene has been investigated. Although a carbonyl conjugated alkene is present, the arylpalladium species selectively inserts into the C3-4 double bond, and a subsequent C-H activation reaction with a neighboring phenyl group gives the indene derivatives with a tetrasubstituted olefin moiety.

Entities:  

Year:  2006        PMID: 17047794     DOI: 10.1039/b607684j

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


  1 in total

1.  Palladium-catalyzed synthesis of cyclopentane-fused benzocyclobutenes via tandem directed carbopalladation/C-H bond functionalization.

Authors:  Myra Beaudoin Bertrand; John P Wolfe
Journal:  Org Lett       Date:  2007-07-07       Impact factor: 6.005

  1 in total

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