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Volumn 6, Issue 10, 1995, Pages 2593-2596

Catalytic asymmetric hydroboration with heterotopic P-N ligands: Trends in enantioselectivity with increased steric demand

Author keywords

[No Author keywords available]

Indexed keywords

ALKANOL; PHENOL DERIVATIVE;

EID: 0028869146     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/0957-4166(95)00340-U     Document Type: Article
Times cited : (92)

References (26)
  • 19
    • 84914091465 scopus 로고    scopus 로고
    • Valk, J-M; Claridge, T. D. W.; Brown, J. M.; Hibbs D.; Hursthouse, M. B. Tetrahedron : Asymmetry, this issue.
  • 21
    • 84914091463 scopus 로고    scopus 로고
    • Hayashi, T.; Matsumoto Y.; Ito, Y.; Tetrahedron : Asymmetry, 1991, 2, 601; in a recent paper, Togni and co-workers have achieved e.e.s up to 98.5% (albeit moderate regioselectivities) in asymmetric hydroboration of styrene with the Rh complexes of 1-diarylphosphino-2-N-pyrazolylethylferrocenes: Schneyder, A.; Hintermann, L.; Togni, A., Angew. Chem. Int. Ed., 1995, 34, 931.
  • 22
    • 84994437953 scopus 로고
    • Ligand Electronic Effects in Asymmetric Catalysis: Enhanced Enantioselectivity in the Asymmetric Hydrocyanation of Vinylarenes
    • This seems to be a sensitive steric probe; in other recent asymmetric catalyses 2-vinylnaphthalene gives comparable or superior results to styrene:
    • (1994) Journal of the American Chemical Society , vol.116 , pp. 9869-9882
    • Casalnuovo1    RajanBabu2    Ayers3    Warren4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.