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Volumn 52, Issue 24, 1996, Pages 8209-8222

Indole as a tool in synthesis. Indolenine approach to 4,5-epoxy-10-normorphinans

Author keywords

[No Author keywords available]

Indexed keywords

BETULACEAE;

EID: 0029889802     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4020(96)00378-X     Document Type: Article
Times cited : (14)

References (52)
  • 4
    • 77957027656 scopus 로고
    • Cordell, G.; Brossi, A. Eds.; Academic Press Inc.: San Diego. In addition, see
    • (a) For a review, see: Szántay, Cs.; Dörnyei, G.; Blaskó, G. The Morphine Alkaloids in The Alkaloids; Cordell, G.; Brossi, A. Eds.; Academic Press Inc.: San Diego, 1994, Vol. 45, p. 127. In addition, see:
    • (1994) The Morphine Alkaloids in The Alkaloids , vol.45 , pp. 127
    • Szántay, C.1    Dörnyei, G.2    Blaskó, G.3
  • 18
    • 0004034466 scopus 로고
    • Eur. Pat. Appl. EP 9 780, 1980
    • For closely related 10-nor analogs, see: (a) Ciganek, E. Eur. Pat. Appl. EP 9 780, 1980; Chem. Abstr. 1980, 93, 220720v.
    • (1980) Chem. Abstr. , vol.93
    • Ciganek, E.1
  • 19
    • 9744259856 scopus 로고
    • US Patent US 4 243 668, 1981
    • (b) Ciganek, E. US Patent US 4 243 668, 1981; Chem. Abstr. 1981, 95, 80924d.
    • (1981) Chem. Abstr. , vol.95
    • Ciganek, E.1
  • 21
    • 0040483283 scopus 로고
    • US Patent US 4 751 306, 1988
    • (d) Ciganek, E.; Wong, B. US Patent US 4 751 306, 1988; Chem. Abstr. 1988, 109, 128987p.
    • (1988) Chem. Abstr. , vol.109 , pp. 128987
    • Ciganek, E.1    Wong, B.2
  • 23
    • 85029994545 scopus 로고    scopus 로고
    • note
    • For homogeneity, morphine numbering was used in the whole article.
  • 24
    • 85029974593 scopus 로고    scopus 로고
    • note
    • +· 8), 154 (25), 149 (21).
  • 25
    • 0003009874 scopus 로고
    • For reviews on the intramolecular Diels-Alder reaction, see: (a) Ciganek, E. Org. Reactions, 1984, 32, 1.
    • (1984) Org. Reactions , vol.32 , pp. 1
    • Ciganek, E.1
  • 28
    • 0039298195 scopus 로고
    • Trost, B.M.; Fleming, I. Eds.; Pergamon: Oxford
    • (d) Roush, W.R. in Comprehensive Organic Synthesis; Trost, B.M.; Fleming, I. Eds.; Pergamon: Oxford, 1991, 32, 1549.
    • (1991) Comprehensive Organic Synthesis , vol.32 , pp. 1549
    • Roush, W.R.1
  • 29
    • 33845551047 scopus 로고
    • For some references for the preparation of yohimbine related compounds via decahydroisoquinoline intermediate, obtained by Diels-Alder reaction, see: (a) Martin, S.F.; Williamson, S.A.; Gist, R.P. Smith, K.M. J. Org. Chem. 1983, 48, 5170.
    • (1983) J. Org. Chem. , vol.48 , pp. 5170
    • Martin, S.F.1    Williamson, S.A.2    Gist, R.P.3    Smith, K.M.4
  • 44
    • 85029985580 scopus 로고
    • Sharkova, N.M.; Kucherova, N.F.; Portnova, S.L.; Zagorevskii, V.A. Khim. Geterotsikl. Soedin. 1968, 131; Chem. Abstr. 1968, 69, 86857u.
    • (1968) Chem. Abstr. , vol.69
  • 45
    • 85077749433 scopus 로고
    • For a review on silyl enol ethers, see: Brownbridge, P. Synthesis 1983, 85.
    • (1983) Synthesis , pp. 85
    • Brownbridge, P.1
  • 46
    • 85029991776 scopus 로고    scopus 로고
    • note
    • Heats of formation were calculated in the "Laboratoire de Chimie Théorique" (URA CNRS 510), Université de Nancy I by B. Maigret and A. Cartier using AM1 calculation method.
  • 51
    • 85029989979 scopus 로고    scopus 로고
    • note
    • 3).
  • 52
    • 85030000298 scopus 로고    scopus 로고
    • note
    • Crystallographic data were deposited at the Cambridge Crystallographic Data Centre, Lensfield Road, Cambridge, CB2, 1EW, UK.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.