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Volumn 41, Issue 17, 1985, Pages 3559-3568

Alkaloid synthesis via the intramolecular imidate methylide 1,3-dipolar cycloaddition reaction

Author keywords

[No Author keywords available]

Indexed keywords


EID: 0001432168     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(01)96709-2     Document Type: Article
Times cited : (61)

References (27)
  • 8
    • 0000627841 scopus 로고
    • Additional references of pertinence to the generation of heteratom substituted imidate methylides include
    • (1983) J. Org. Chem. , vol.48 , pp. 4773
    • Vedejs1    West2
  • 14
    • 0002126741 scopus 로고
    • 1058. The protonation of tryptamine derivatives in acidic media
    • This result is in accord with the known propensity of the physostigmine B,C-ring junction to undergo reversible opening upon exposure to silica gel
    • (1964) Journal of the Chemical Society (Resumed) , pp. 5510
    • Jackson1    Smith2
  • 18
    • 77957094911 scopus 로고
    • R.H.F. Manske, Academic Press, New York
    • (1967) The Alkaloids , vol.9 , pp. 483
    • Hill1
  • 26
    • 0000469898 scopus 로고
    • An additional failed attempt to effect a related intramolecular imidate methylide cycloaddition has recently been reported
    • (1984) J. Org. Chem. , vol.49 , pp. 3314
    • Padwa1    Haffmanns2    Thomas3
  • 27
    • 84918066618 scopus 로고    scopus 로고
    • The geometry of the enamine double bond present in 46 was shown to be Z by differential nuclear Overhauser spectroscopy.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.