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Volumn 113, Issue 23, 1991, Pages 8975-8976

[1 + 4] Cycloaddition of Vinyl Isocyanates with Alkyl Isocyanides. Formal Total Synthesis of Erysotrine

Author keywords

[No Author keywords available]

Indexed keywords

ALKALOID; ERYSOTRINE; UNCLASSIFIED DRUG;

EID: 0026344585     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja00023a072     Document Type: Article
Times cited : (74)

References (25)
  • 19
    • 0015973559 scopus 로고
    • The proton at C11c in compound 9 appeared as a doublet at δ 3.13 with J = 11 Hz. Typical trans J values for similar protons in naturally occurring alkaloids range between 10 and 12 Hz
    • The proton at C11c in compound 9 appeared as a doublet at δ 3.13 with J = 11 Hz. Typical trans J values for similar protons in naturally occurring alkaloids range between 10 and 12 Hz: (a) Torssell, K. Tetrahedron Lett. 1974, 623.
    • (1974) Tetrahedron Lett. , pp. 623
    • Torssell, K.1
  • 21
    • 0002696069 scopus 로고
    • For a recent review of the Erythrina alkaloids, see: Rodrigo, R. G. A., Ed.; Academic Press: New York
    • For a recent review of the Erythrina alkaloids, see: Dyke, S. F.; Quessy, S. N. In The Alkaloids; Rodrigo, R. G. A., Ed.; Academic Press: New York, 1981; Vol. XVIII, p 1.
    • (1981) The Alkaloids , vol.XVIII , pp. 1
    • Dyke, S.F.1    Quessy, S.N.2
  • 22
    • 33847802966 scopus 로고
    • Prepared from commercially available 4-methoxycyclohexane-carboxylic acid via a selenenylation-selenoxide elimination sequence
    • Prepared from commercially available 4-methoxycyclohexane-carboxylic acid via a selenenylation-selenoxide elimination sequence: Reich, H. J.; Renga, J. M.; Reich, I. L. J. Am. Chem. Soc. 1975, 97, 5434.
    • (1975) J. Am. Chem. Soc. , vol.97 , pp. 5434
    • Reich, H.J.1    Renga, J.M.2    Reich, I.L.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.