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Volumn 36, Issue 26, 1995, Pages 4689-4692

Exo- and endo-6-hydroxy- and 6,7-epoxytropanes; Total synthesis of scopine, pseudoscopine, and nor-derivatives

Author keywords

[No Author keywords available]

Indexed keywords

PSEUDOSCOPINE; SCOPINE; TROPANE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0029000802     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4039(95)00836-2     Document Type: Article
Times cited : (14)

References (21)
  • 8
    • 85005550758 scopus 로고
    • Synthetic Studies on the 1-Hydroxy Nortropane System,-Part III:1Total Enantioselective Synthesis of (-)-Calystegine B2
    • (1992) Synlett , pp. 969
    • Boyer1    Lallemand2
  • 13
    • 37049049244 scopus 로고
    • 698. The stereochemistry of the tropane alkaloids. Part XII. The total synthesis of scopolamine
    • Epoxidation of 6,7-dehydrotropine (which is not readily available) was reported in this work but we and others have established that this methodology gives low conversions.
    • (1959) Journal of the Chemical Society (Resumed) , pp. 3461
    • Dobó1    Fodor2    Janzsó3    Koczor4    Tóth5    Vincze6
  • 14
    • 84872140994 scopus 로고
    • Exo-epoxidation of bicyclic alkenes proceeds more efficiently when the nitrogen bears an alkoxycarbonyl group:, University of Leicester, and ref. 6 above
    • (1991) Ph.D. thesis
    • Howarth1
  • 15
    • 84913981423 scopus 로고    scopus 로고
    • Hemmings, D.; Malpass, J.R. work in progress.
  • 16
    • 84913981422 scopus 로고    scopus 로고
    • Justice, D.E.; Malpass, J.R. Tetrahedron Letters, accompanying paper.
  • 20
    • 84913981421 scopus 로고    scopus 로고
    • These amines were stored and handled as the hydrochloride salts.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.