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Volumn 7, Issue 16, 2009, Pages 3258-3263

Synthesis of highly substituted allylic alcohols by a regio- and stereo-defined CuCl-mediated carbometallation reaction of 3-aryl-substituted secondary propargylic alcohols with Grignard reagents

Author keywords

[No Author keywords available]

Indexed keywords

ALLYLIC ALCOHOL; ELECTROPHILES; GRIGNARD REAGENT; METAL ATOMS; METALLACYCLIC INTERMEDIATES; OPTICALLY ACTIVE; OXYGEN ATOM; PROPARGYLIC ALCOHOLS; STEREO-SELECTIVE;

EID: 68149179621     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/b903769a     Document Type: Article
Times cited : (24)

References (27)
  • 8
    • 33845215822 scopus 로고    scopus 로고
    • For an excellent review on carbometalation of alkynes, see:
    • D. Zhang J. M. Ready J. Am. Chem. Soc. 2006 128 15050
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 15050
    • Zhang, D.1    Ready, J.M.2
  • 10
    • 0000458209 scopus 로고
    • For a review on carbometallation of alkynes containing adjacent heteroatoms, see:
    • A. H. Hoveyda D. A. Evans G. C. Fu Chem. Rev. 1993 93 1307
    • (1993) Chem. Rev. , vol.93 , pp. 1307
    • Hoveyda, A.H.1    Evans, D.A.2    Fu, G.C.3
  • 11
    • 68149175354 scopus 로고    scopus 로고
    • For a review on the stereocontrolled synthesis of tetrasubstituted olefins, see:
    • G. F. Alex F. Pat Tetrahedron 2001 57 5899
    • (2001) Tetrahedron , vol.57 , pp. 5899
    • Alex, G.F.1    Pat, F.2
  • 12
    • 36849088075 scopus 로고    scopus 로고
    • For carbometallation of propargylic alcohols affording regioisomeric mixtures, see:
    • A. B. Flynn W. W. Ogilvie Chem. Rev. 2007 107 4698
    • (2007) Chem. Rev. , vol.107 , pp. 4698
    • Flynn, A.B.1    Ogilvie, W.W.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.