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Volumn 52, Issue 4, 1996, Pages 1389-1398

A Michael initiated - condensation - elimination sequence for the stereoselective synthesis of maleate derivatives

Author keywords

[No Author keywords available]

Indexed keywords

MALEIC ACID DERIVATIVE;

EID: 0030068386     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4020(95)00965-5     Document Type: Article
Times cited : (8)

References (30)
  • 1
    • 0001538227 scopus 로고
    • 2 carbon centres
    • Trost, B.M. Ed.; Pergamon: Oxford
    • 2 Carbon Centres. In Comprehensive Organic Synthesis, Trost, B.M. Ed.; Pergamon: Oxford, Vol. 3, 1991, pp 435;
    • (1991) Comprehensive Organic Synthesis , vol.3 , pp. 435
    • Tamoa, K.1
  • 2
    • 0000891348 scopus 로고
    • 2 carbon centres
    • Trost, B.M. Ed.; Pergamon: Oxford
    • 2 Carbon Centres. In Comprehensive Organic Synthesis, Trost, B.M. Ed.; Pergamon: Oxford, Vol. 3, 1991, pp 481 and
    • (1991) Comprehensive Organic Synthesis , vol.3 , pp. 481
    • Knight, D.W.1
  • 3
    • 0000509322 scopus 로고
    • 2 and sp carbon centres
    • Trost, B.M. Ed.; Pergamon: Oxford
    • 2 and sp Carbon Centres. In Comprehensive Organic Synthesis, Trost, B.M. Ed.; Pergamon: Oxford. Vol. 3, 1991, pp 521.
    • (1991) Comprehensive Organic Synthesis , vol.3 , pp. 521
    • Sonogashira, K.1
  • 4
    • 0001522634 scopus 로고
    • Carbometallation of alkenes and alkynes
    • Trost, B.M. Ed.; Pergamon: Oxford
    • For a recent overview see Knochel, P. Carbometallation of Alkenes and Alkynes. In Comprehensive Organic Synthesis, Trost, B.M. Ed.; Pergamon: Oxford, Vol. 4, 1991, pp 865.
    • (1991) Comprehensive Organic Synthesis , vol.4 , pp. 865
    • Knochel, P.1
  • 7
    • 0343066545 scopus 로고
    • Organometallics in synthesis: Main group elements
    • Pattenden, G. Ed., RSC: Cambridge, Ch. 6ii, and previous articles in that series
    • c. Wills, M. Organometallics in Synthesis: Main Group Elements. In General and Synthetic Methods, Pattenden, G. Ed., RSC: Cambridge, 1994, Vol. 16, Ch. 6ii, pp320 and previous articles in that series.
    • (1994) General and Synthetic Methods , vol.16 , pp. 320
    • Wills, M.1
  • 12
    • 85031218722 scopus 로고    scopus 로고
    • Ger. Pat., 2155133
    • A similar sequence operates in the Baylis-Hillman reaction a. Baylis, A.B.; Hillman, M.E. Ger. Pat., 2155133; Chem. Abs., 1972, 77, 34174q. For some recent examples see
    • Baylis, A.B.1    Hillman, M.E.2
  • 13
    • 4243830773 scopus 로고
    • A similar sequence operates in the Baylis-Hillman reaction a. Baylis, A.B.; Hillman, M.E. Ger. Pat., 2155133; Chem. Abs., 1972, 77, 34174q. For some recent examples see
    • (1972) Chem. Abs. , vol.77
  • 22
    • 0027422282 scopus 로고
    • For other anion mediated cascade sequences developed within our group see a. Harrowven, D.C. Tetrahedron, 1993, 49, 9039;
    • (1993) Tetrahedron , vol.49 , pp. 9039
    • Harrowven, D.C.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.