Transition Metal Catalyzed Alkylation at sp^3-, sp^2-, and sp-Carbons

    • KAMBE Nobuaki
    • Department of Applied Chemistry, Faculty of Engineering, Osaka University
    • TERAO Jun
    • Department of Energy and Hydrocarbon Chemistry, Graduate School of Engineering, Kyoto University
    • IWASAKI Takanori
    • Department of Applied Chemistry, Faculty of Engineering, Osaka University

Abstract

Transition metal catalyzed alkylation reactions resulting in cross-coupling and multicomponent-coupling are described. These reactions proceed efficiently under mild conditions using a combination of transition metal catalysts and alkyl (pseudo)halides in the presence of Grignard reagents and represent the practical routes to the alkylation of sp3-, sp2-, and sp-carbons. Anionic transition metal complexes play important roles as active catalytic species for SN2 and electron transfer processes in reactions with alkyl halides. The carbometalation of C-C unsaturated bonds with alkylmetal species is also a promising tool for the introduction of alkyl groups.

Journal

Journal of Synthetic Organic Chemistry, Japan  

Journal of Synthetic Organic Chemistry, Japan 69(11), 1271-1281, 2011-11-01 

The Society of Synthetic Organic Chemistry, Japan

References:  72

You must have a user ID to see the references.If you already have a user ID, please click "Login" to access the info.New users can click "Sign Up" to register for an user ID.

Codes

  • NII Article ID (NAID) :
    10029928151
  • NII NACSIS-CAT ID (NCID) :
    AN0024521X
  • Text Lang :
    ENG
  • Article Type :
    ART
  • ISSN :
    00379980
  • NDL Article ID :
    023324950
  • NDL Source Classification :
    ZP11(科学技術--化学・化学工業--有機化学・有機化学工業)
  • NDL Call No. :
    Z17-256
  • Databases :
    CJP  NDL  J-STAGE 

Share