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Volumn 39, Issue 43, 1998, Pages 7947-7950

Efficient and practical method for synthesizing optically active γ- trityloxymethyl-α-alkylidene-γ butyrolactones using ti(II)-mediated intramolecular nucleophilic acyl substitution reaction

Author keywords

Coupling reactions; Epoxides; Lactones; Titanium and compounds

Indexed keywords

GAMMA BUTYROLACTONE DERIVATIVE; TITANIUM; TRITYL DERIVATIVE;

EID: 0032558633     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(98)01769-9     Document Type: Article
Times cited : (14)

References (20)
  • 1
    • 0018114921 scopus 로고
    • [1] For synthesis of a variety of chiral compounds and natural products using γalkoxymethyl-α-alkylidene-γ-butyrolactone intermediates, see: a) Tomioka K, Mizuguchi H, Koga K. Tetrahedron Lett. 1978;4687-4690.
    • (1978) Tetrahedron Lett. , pp. 4687-4690
    • Tomioka, K.1    Mizuguchi, H.2    Koga, K.3
  • 11
    • 0000523862 scopus 로고
    • [2] Taniguchi M, Koga K, Yamada S. Tetrahedron 1974;30:3547-3552. Takano S, Goto E, Hirama M, Ogasawara K. Heterocycles 1981;16:381-385. Takano S, Goto E, Hirama M, Ogasawara K. Heterocycles 1981;16:951-954.
    • (1974) Tetrahedron , vol.30 , pp. 3547-3552
    • Taniguchi, M.1    Koga, K.2    Yamada, S.3
  • 12
    • 0000492501 scopus 로고
    • [2] Taniguchi M, Koga K, Yamada S. Tetrahedron 1974;30:3547-3552. Takano S, Goto E, Hirama M, Ogasawara K. Heterocycles 1981;16:381-385. Takano S, Goto E, Hirama M, Ogasawara K. Heterocycles 1981;16:951-954.
    • (1981) Heterocycles , vol.16 , pp. 381-385
    • Takano, S.1    Goto, E.2    Hirama, M.3    Ogasawara, K.4
  • 13
    • 0010243984 scopus 로고
    • [2] Taniguchi M, Koga K, Yamada S. Tetrahedron 1974;30:3547-3552. Takano S, Goto E, Hirama M, Ogasawara K. Heterocycles 1981;16:381-385. Takano S, Goto E, Hirama M, Ogasawara K. Heterocycles 1981;16:951-954.
    • (1981) Heterocycles , vol.16 , pp. 951-954
    • Takano, S.1    Goto, E.2    Hirama, M.3    Ogasawara, K.4
  • 14
    • 0029100697 scopus 로고
    • [3] Kasatkin A, Okamoto S, Sato F. Tetrahedron Lett. 1995;36:6075-6078. Okamoto S, Kasatkin A, Zubaidha PK, Sato F. J. Am. Chem. Soc. 1996;118:2208-2216. Okamoto S, Iwakubo M, Kobayashi K, Sato F. J. Am. Chem. Soc. 1997;11:6984-6990.
    • (1995) Tetrahedron Lett. , vol.36 , pp. 6075-6078
    • Kasatkin, A.1    Okamoto, S.2    Sato, F.3
  • 15
    • 0029984653 scopus 로고    scopus 로고
    • [3] Kasatkin A, Okamoto S, Sato F. Tetrahedron Lett. 1995;36:6075-6078. Okamoto S, Kasatkin A, Zubaidha PK, Sato F. J. Am. Chem. Soc. 1996;118:2208-2216. Okamoto S, Iwakubo M, Kobayashi K, Sato F. J. Am. Chem. Soc. 1997;11:6984-6990.
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 2208-2216
    • Okamoto, S.1    Kasatkin, A.2    Zubaidha, P.K.3    Sato, F.4
  • 16
    • 0030797504 scopus 로고    scopus 로고
    • [3] Kasatkin A, Okamoto S, Sato F. Tetrahedron Lett. 1995;36:6075-6078. Okamoto S, Kasatkin A, Zubaidha PK, Sato F. J. Am. Chem. Soc. 1996;118:2208-2216. Okamoto S, Iwakubo M, Kobayashi K, Sato F. J. Am. Chem. Soc. 1997;11:6984-6990.
    • (1997) J. Am. Chem. Soc. , vol.11 , pp. 6984-6990
    • Okamoto, S.1    Iwakubo, M.2    Kobayashi, K.3    Sato, F.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.