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Volumn 58, Issue 25, 1993, Pages 6949-6951

Catalytic Asymmetric Synthesis of Either Enantiomer of Physostigmine. Formation of Quaternary Carbon Centers with High Enantioselection by Intramolecular Heck Reactions of (Z)-2-Butenanilides

Author keywords

[No Author keywords available]

Indexed keywords

PHYSOSTIGMINE;

EID: 0027772652     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo00077a005     Document Type: Article
Times cited : (160)

References (34)
  • 1
    • 77957022703 scopus 로고
    • For a review of alkaloids of the Calabar bean, see
    • For a review of alkaloids of the Calabar bean, see: Takano, S.; Ogasawara, K. Alkaloids 1989, 36, 225–251.
    • (1989) Alkaloids , vol.36 , pp. 225-251
    • Takano, S.1    Ogasawara, K.2
  • 2
    • 0025483995 scopus 로고
    • For recent reviews of pharmacology, see: (a)
    • For recent reviews of pharmacology, see: (a) Brossi, A. J. Med. Chem. 1990, 33, 2311.
    • (1990) J. Med. Chem. , vol.33 , pp. 2311
    • Brossi, A.1
  • 4
    • 0000353442 scopus 로고
    • For asymmetric total syntheses published since the most recent review, see: (a)
    • For asymmetric total syntheses published since the most recent review, see: (a) Takano, S.; Moriya, M.; Iwabuchi, Y.; Ogasawara K. Chem. Lett. 1990, 109.
    • (1990) Chem. Lett. , pp. 109
    • Takano, S.1    Moriya, M.2    Iwabuchi, Y.3    Ogasawara, K.4
  • 11
    • 33845281518 scopus 로고
    • For our previous studies of forming 3,3-disubstituted 2-oxindoles by intramolecular Heck reactions, see: (a)
    • For our previous studies of forming 3,3-disubstituted 2-oxindoles by intramolecular Heck reactions, see: (a) Abelman, M. M.; Oh, T.; Overman, L. E. J. Org. Chem. 1987, 52, 4130.
    • (1987) J. Org. Chem. , vol.52 , pp. 4130
    • Abelman, M.M.1    Oh, T.2    Overman, L.E.3
  • 15
    • 0001643522 scopus 로고
    • The synthesis of a racemic hexahydropyrrolo[2,3-b]indole by intramolecular Heck cyclization of a pyrrolidin-2-one aminal has been described by Hoffmann; see
    • The synthesis of a racemic hexahydropyrrolo[2,3-b]indole by intramolecular Heck cyclization of a pyrrolidin-2-one aminal has been described by Hoffmann; see: Hoffmann, H. M. R.; Schmidt, B.; Wolff, S. Tetrahedron 1989, 45, 6113.
    • (1989) Tetrahedron , vol.45 , pp. 6113
    • Hoffmann, H.M.R.1    Schmidt, B.2    Wolff, S.3
  • 16
    • 0000438986 scopus 로고
    • For previous examples of asymmetric Heck reactions, see ref 6c and: (a)
    • For previous examples of asymmetric Heck reactions, see ref 6c and: (a) Sato, Y.; Sodeoka M.; Shibasaki, M. J. Org. Chem. 1989, 54, 4738.
    • (1989) J. Org. Chem. , vol.54 , pp. 4738
    • Sato, Y.1    Sodeoka, M.2    Shibasaki, M.3
  • 28
    • 85022544005 scopus 로고
    • For a brief review of asymmetric Heck reactions, see: (m), Jpn.
    • For a brief review of asymmetric Heck reactions, see: (m) Shibasaki, M.; Sato, Y.; Kagechika, K. J. Synth. Org. Chem., Jpn. 1992, 50, 826.
    • (1992) J. Synth. Org. Chem. , vol.50 , pp. 826
    • Shibasaki, M.1    Sato, Y.2    Kagechika, K.3
  • 34
    • 49549139072 scopus 로고
    • BOP = (benzotriazol-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate
    • BOP = (benzotriazol-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate: Castro, B.; Dormoy, J. R.; Evin, G.; Selve, C. Tetrahedron Lett. 1975, 1219.
    • (1975) Tetrahedron Lett. , pp. 1219
    • Castro, B.1    Dormoy, J.R.2    Evin, G.3    Selve, C.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.