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Volumn , Issue 5, 1999, Pages 535-544

Enantioselective carbometallation of unactivated olefins

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[No Author keywords available]

Indexed keywords


EID: 33746549884     PISSN: 0300922X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (62)

References (87)
  • 19
    • 33746497067 scopus 로고    scopus 로고
    • Reaction of racemic allylic alcohol, and 10 mol% of racemic complex 2 affords the product with little selectivity.
    • Reaction of racemic allylic alcohol, and 10 mol% of racemic complex 2 affords the product with little selectivity.
  • 28
    • 0030598055 scopus 로고    scopus 로고
    • 1996,52, 10025.
    • For a mechanistic discussion on the stereochemical outcome of benzylic organolithium derivatives, see: C. M. Lichtenfeld, and H. Ahlbrecht, Tetrahedron, 1996,52, 10025.
    • Tetrahedron
    • Ahlbrecht, H.1
  • 29
    • 33746532040 scopus 로고    scopus 로고
    • The reaction was perfomed on a 50 mmol scale of cinnamyl alcohol in the presence of 5% sparteine. However, in this case a slightly lower yield is obtained due to the telomerization of ULi on cinnamyl alcoholate leading to a dimer.
    • The reaction was perfomed on a 50 mmol scale of cinnamyl alcohol in the presence of 5% sparteine. However, in this case a slightly lower yield is obtained due to the telomerization of ULi on cinnamyl alcoholate leading to a dimer.
  • 40
    • 0029742482 scopus 로고    scopus 로고
    • 1996,35, 1657, and references cited therein.
    • For a highlight see C. Bolm, F. Bienewald, and A. Seger, Angew. Client., Int. Ed. Engt., 1996,35, 1657, and references cited therein.
    • Angew. Client., Int. Ed. Engt.
    • Seger, A.1
  • 41
    • 0029063782 scopus 로고    scopus 로고
    • 1995, 36, 3695
    • The formation of cyclopropane by 1,3-elimination between an organo-geHi-bismetallic, and a methoxymethyl ether has already been described: (a) I. Marek, D. Beruhen, and J. F. Normant, Tetrahedron Lett., 1995, 36, 3695;
    • Tetrahedron Lett.
    • Marek, I.1    Beruhen, D.2    Normant, J.F.3
  • 44
    • 0010597031 scopus 로고    scopus 로고
    • 1995,1197, and references cited therein
    • For some representative formations of chiral cyclopropanes, see (a) A. B. Charette, and J. F. Marcoux, Synlett, 1995,1197, and references cited therein;
    • Synlett
    • Charette, A.B.1    Marcoux, J.F.2
  • 53
    • 33746580971 scopus 로고    scopus 로고
    • 1992, 33, 6527; (b) A. Krief, M. Höbe, W. Dumont, E. Badaoui, E. Guittet, and G. Evrard, Tetrahedron Lett., 1992, 33, 3381.
    • (a) A. Krief, and M. Höbe, Tetrahedron Lett., 1992, 33, 6527; (b) A. Krief, M. Höbe, W. Dumont, E. Badaoui, E. Guittet, and G. Evrard, Tetrahedron Lett., 1992, 33, 3381.
    • Tetrahedron Lett.
    • Krief, A.1    Höbe, M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.