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Volumn 13, Issue 15, 2011, Pages 3968-3971

A tertiary amine as a hydride donor: Trichlorosilyl triflate-mediated conjugate reduction of unsaturated ketones

Author keywords

[No Author keywords available]

Indexed keywords

AMINE; KETONE; MESYLIC ACID DERIVATIVE;

EID: 79961067087     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol2014895     Document Type: Article
Times cited : (45)

References (33)
  • 5
    • 85077888556 scopus 로고
    • For imidazoline or thiazoline-promoted reductions, see
    • For imidazoline or thiazoline-promoted reductions, see: Chikashita, H.; Miyazaki, M.; Itoh, K. Synthesis 1984, 308
    • (1984) Synthesis , pp. 308
    • Chikashita, H.1    Miyazaki, M.2    Itoh, K.3
  • 11
    • 0142109794 scopus 로고
    • For lithium amide-promoted reductions, see
    • For lithium amide-promoted reductions, see: Woo, E. P.; Mak, K. T. Tetrahedron Lett. 1974, 15, 4095
    • (1974) Tetrahedron Lett. , vol.15 , pp. 4095
    • Woo, E.P.1    Mak, K.T.2
  • 18
    • 1242316320 scopus 로고    scopus 로고
    • For metal-mediated reductions with tertiary amines, see
    • For metal-mediated reductions with tertiary amines, see: Clerici, A.; Pastori, N.; Porta, O. Tetrahedron Lett. 2004, 45, 1825
    • (2004) Tetrahedron Lett. , vol.45 , pp. 1825
    • Clerici, A.1    Pastori, N.2    Porta, O.3
  • 29
    • 0002952831 scopus 로고
    • For preparation of trichlorosilyl triflate, see
    • For preparation of trichlorosilyl triflate, see: Bassindale, A. R.; Stout, T. J. Organomet. Chem. 1984, 271, C1
    • (1984) J. Organomet. Chem. , vol.271 , pp. 1
    • Bassindale, A.R.1    Stout, T.2
  • 32
    • 0001510055 scopus 로고    scopus 로고
    • For generation of iminium intermediates from tertiary amines, see
    • For generation of iminium intermediates from tertiary amines, see: Bharathi, P.; Periasamy, M. Org. Lett. 1999, 1, 857
    • (1999) Org. Lett. , vol.1 , pp. 857
    • Bharathi, P.1    Periasamy, M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.