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Volumn 56, Issue 12, 2000, Pages 1733-1737

An easy deoxygenation of conjugated epoxides

Author keywords

Deoxygenation; Isomerisation; Oxiranes

Indexed keywords

CALCIFEDIOL; CHOLESTANE DERIVATIVE; EPOXIDE;

EID: 0034677829     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(99)01083-2     Document Type: Article
Times cited : (28)

References (28)
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    • 0000533091 scopus 로고
    • See for example: Rajan Babu, T. V.; Nugent, W. A.; Beattie, M. S. J. Am. Chem. Soc. 1990, 112, 6408-6409. Gable, K. P.; Zhuravlev, F. A.; Yokochi, A. F. T. J. Chem. Soc., Chem Commun. 1998, 799-800. Wong, H. N. C.; Fok, C. C. M.; Wong, T. Heterocycles 1987, 26, 1345-1382. Martin, M. G.; Ganem, B. Tetrahedron Lett. 1984, 24, 251-254. Mandal, A. K.; Mahajan, S. W. Tetrahedron 1988, 44, 2293-2300.
    • (1990) J. Am. Chem. Soc. , vol.112 , pp. 6408-6409
    • Rajan Babu, T.V.1    Nugent, W.A.2    Beattie, M.S.3
  • 2
    • 0342765378 scopus 로고    scopus 로고
    • See for example: Rajan Babu, T. V.; Nugent, W. A.; Beattie, M. S. J. Am. Chem. Soc. 1990, 112, 6408-6409. Gable, K. P.; Zhuravlev, F. A.; Yokochi, A. F. T. J. Chem. Soc., Chem Commun. 1998, 799-800. Wong, H. N. C.; Fok, C. C. M.; Wong, T. Heterocycles 1987, 26, 1345-1382. Martin, M. G.; Ganem, B. Tetrahedron Lett. 1984, 24, 251-254. Mandal, A. K.; Mahajan, S. W. Tetrahedron 1988, 44, 2293-2300.
    • (1998) J. Chem. Soc., Chem Commun. , pp. 799-800
    • Gable, K.P.1    Zhuravlev, F.A.2    Yokochi, A.F.T.3
  • 3
    • 0001580966 scopus 로고
    • See for example: Rajan Babu, T. V.; Nugent, W. A.; Beattie, M. S. J. Am. Chem. Soc. 1990, 112, 6408-6409. Gable, K. P.; Zhuravlev, F. A.; Yokochi, A. F. T. J. Chem. Soc., Chem Commun. 1998, 799-800. Wong, H. N. C.; Fok, C. C. M.; Wong, T. Heterocycles 1987, 26, 1345-1382. Martin, M. G.; Ganem, B. Tetrahedron Lett. 1984, 24, 251-254. Mandal, A. K.; Mahajan, S. W. Tetrahedron 1988, 44, 2293-2300.
    • (1987) Heterocycles , vol.26 , pp. 1345-1382
    • Wong, H.N.C.1    Fok, C.C.M.2    Wong, T.3
  • 4
    • 0000022001 scopus 로고
    • See for example: Rajan Babu, T. V.; Nugent, W. A.; Beattie, M. S. J. Am. Chem. Soc. 1990, 112, 6408-6409. Gable, K. P.; Zhuravlev, F. A.; Yokochi, A. F. T. J. Chem. Soc., Chem Commun. 1998, 799-800. Wong, H. N. C.; Fok, C. C. M.; Wong, T. Heterocycles 1987, 26, 1345-1382. Martin, M. G.; Ganem, B. Tetrahedron Lett. 1984, 24, 251-254. Mandal, A. K.; Mahajan, S. W. Tetrahedron 1988, 44, 2293-2300.
    • (1984) Tetrahedron Lett. , vol.24 , pp. 251-254
    • Martin, M.G.1    Ganem, B.2
  • 5
    • 0000800856 scopus 로고
    • See for example: Rajan Babu, T. V.; Nugent, W. A.; Beattie, M. S. J. Am. Chem. Soc. 1990, 112, 6408-6409. Gable, K. P.; Zhuravlev, F. A.; Yokochi, A. F. T. J. Chem. Soc., Chem Commun. 1998, 799-800. Wong, H. N. C.; Fok, C. C. M.; Wong, T. Heterocycles 1987, 26, 1345-1382. Martin, M. G.; Ganem, B. Tetrahedron Lett. 1984, 24, 251-254. Mandal, A. K.; Mahajan, S. W. Tetrahedron 1988, 44, 2293-2300.
    • (1988) Tetrahedron , vol.44 , pp. 2293-2300
    • Mandal, A.K.1    Mahajan, S.W.2
  • 7
  • 11
    • 0033529974 scopus 로고    scopus 로고
    • The same selectivity was found with other halogens during a process in which 2-haloenones were prepared from α,β unsaturated ketones: Use of NaI or LiI lead to similar results meaning an absence of counter ion effects.
    • The same selectivity was found with other halogens during a process in which 2-haloenones were prepared from α,β unsaturated ketones: Righi, G.; Bovicelli, P.; Sperandio, A. Tetrahedron. Lett. 1999, 40, 5889. Use of NaI or LiI lead to similar results meaning an absence of counter ion effects.
    • (1999) Tetrahedron. Lett. , vol.40 , pp. 5889
    • Righi, G.1    Bovicelli, P.2    Sperandio, A.3
  • 15
    • 0343199968 scopus 로고    scopus 로고
    • Characterised comparing 22 with an authentic sample from Sigma company.
    • Characterised comparing 22 with an authentic sample from Sigma company.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.