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Volumn 680, Issue 1-2, 2003, Pages 136-142

Synthesis and reaction of secondary and primary diorganozinc reagents using a boron-zinc exchange reaction. A useful method for the stereo- and regioselective formation of new carbon-carbon bonds

Author keywords

C C coupling; Diastereoselective synthesis; Hydroboration; Transmetallation; Zinc organometallics

Indexed keywords

BORON; CARBON; REAGENT; SILANE DERIVATIVE; ZINC;

EID: 0042890355     PISSN: 0022328X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-328X(03)00237-7     Document Type: Article
Times cited : (37)

References (55)
  • 22
    • 0042963532 scopus 로고    scopus 로고
    • 2BH is to replace the bulky isopinocampheyl ligand by an ethyl group or a hydrogen atom
    • 2BH is to replace the bulky isopinocampheyl ligand by an ethyl group or a hydrogen atom.
  • 24
    • 0003280270 scopus 로고
    • Conjugate addition reactions in organic synthesis
    • J. E. Baldwin, & P. D. Magnus (Eds.), Oxford: Pergamon Press
    • Perlmutter P. Conjugate addition reactions in organic synthesis, in: Baldwin J.E. Magnus P.D. (Eds.), Tetrahedron Organic Chemistry Series 9 1992 Pergamon Press Oxford
    • (1992) Tetrahedron Organic Chemistry Series , vol.9
    • Perlmutter, P.1
  • 32
    • 0001085039 scopus 로고
    • For reviews about substrate controlled diastereoselective hydroborations see
    • For reviews about substrate controlled diastereoselective hydroborations see: K. Burgess, M.J. Ohlmeyer, Chem. Rev. 91 (1991) 1179
    • (1991) Chem. Rev. , vol.91 , pp. 1179
    • Burgess, K.1    Ohlmeyer, M.J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.