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Volumn 53, Issue 48, 1997, Pages 16423-16434

The asymmetric Baylis-Hillman reaction as a template in organic synthesis

Author keywords

[No Author keywords available]

Indexed keywords

ACRYLIC ACID; CAMPHOR; ORGANIC COMPOUND;

EID: 0030827529     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(97)01025-9     Document Type: Conference Paper
Times cited : (58)

References (61)
  • 1
    • 0003417469 scopus 로고
    • Pergamon Press, Oxford
    • For a review of recent trends in organic synthesis, see: Comprehensive Organic Synthesis, Trost, B. M., Ed.; Pergamon Press, Oxford, 1991.
    • (1991) Comprehensive Organic Synthesis
    • Trost, B.M.1
  • 5
    • 0000458209 scopus 로고
    • The use of allylic alcohols to direct reactions has recently been reviewed: Hoveyda, A. H.; Evans, D. A.; Fu, G. C. Chem. Rev. 1993, 93, 1307.
    • (1993) Chem. Rev. , vol.93 , pp. 1307
    • Hoveyda, A.H.1    Evans, D.A.2    Fu, G.C.3
  • 7
    • 0026052599 scopus 로고
    • and references cited within
    • See Isaacs, N. S. Tetrahedron 1991, 47, 8463 and references cited within.
    • (1991) Tetrahedron , vol.47 , pp. 8463
    • Isaacs, N.S.1
  • 10
  • 11
    • 26344479016 scopus 로고    scopus 로고
    • The use of tributylphosphine as a catalyst has been reported previously. See: Miyakoshi, T.; Omichi, H.; Saito, S. Nippon Kagaku Kaishi 1979, 748. See also Chem Abst. 91:123360d.
    • Chem Abst. , vol.91
  • 12
    • 0001461985 scopus 로고
    • The use of triarylphosphines does not lead to the formation of Baylis-Hillman products but rather to Wittig-derived alkenes. See: Morita, K.; Suzuki, Z.; Hirose, H. Bull. Chem. Soc. Jpn. 1968, 41, 2815.
    • (1968) Bull. Chem. Soc. Jpn. , vol.41 , pp. 2815
    • Morita, K.1    Suzuki, Z.2    Hirose, H.3
  • 24
    • 0001399971 scopus 로고
    • and references cited within
    • See Norcross, R. D.; Paterson, I. Chem. Rev. 1995, 95, 2041 and references cited within.
    • (1995) Chem. Rev. , vol.95 , pp. 2041
    • Norcross, R.D.1    Paterson, I.2
  • 25
    • 0010637233 scopus 로고
    • Morrison, J. D., Ed.; Academic: New York
    • For excellent reviews of the aldol reaction, see: a) Heathcock, C. H. in Asymmetric Synthesis; Morrison, J. D., Ed.; Academic: New York, 1984; Vol. 3, pp 112-212.
    • (1984) Asymmetric Synthesis , vol.3 , pp. 112-212
    • Heathcock, C.H.1
  • 27
    • 0000851696 scopus 로고
    • Trost B. M. and Fleming, I., Ed.; Pergamon: Oxford
    • c) Heathcock, C. H. in Comprehensive Organic Synthesis; Trost B. M. and Fleming, I., Ed.; Pergamon: Oxford, 1991; Vol. 2, pp 133-238.
    • (1991) Comprehensive Organic Synthesis , vol.2 , pp. 133-238
    • Heathcock, C.H.1
  • 39
    • 0342930262 scopus 로고    scopus 로고
    • note
    • 32 While these models help to explain the observed stereochemical outcome, they do not represent computationally minimized structures.
  • 44
    • 0029113710 scopus 로고
    • Lafontaine, J. A.; Leahy, J. W. Tetrahedron Lett. 1995, 36, 6029. Provencal, D. P.; Gardelli, C. Lafontaine, J. A.; Leahy, J. W. Tetrahedron Lett. 1995, 36, 6033.
    • (1995) Tetrahedron Lett. , vol.36 , pp. 6029
    • Lafontaine, J.A.1    Leahy, J.W.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.