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Volumn 23, Issue 19, 1982, Pages 2005-2008

Intramolecular azide cycloaddition (IAC) reactions in the indole series - an approach to clavicipitic acid

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Indexed keywords


EID: 0001145334     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)87245-7     Document Type: Article
Times cited : (15)

References (11)
  • 8
    • 33947085599 scopus 로고
    • The addition of phenyl azide to cis- or trans-β-methylstyrene has been shown to provide a single triazoline possessing a 1,5-disposition of phenyl groups in each instance.
    • (1973) J. Am. Chem. Soc. , vol.95 , pp. 7287
    • Houk1    Sims2    Duke3    Strozier4    George5
  • 10
    • 0009593853 scopus 로고
    • Regiospecific cyclization of N-benzoyl-N-methoxymethyl-1-methyl-.ALPHA.,.BETA.-dehydrotryptophan methyl ester to a 5,6-dihydroazepino(5,4,3-cd)indole derivative. A new method for introducing substituents onto the 4-position of indole nucleus.
    • For other efforts directed toward clavicipitic acid, see
    • (1981) Chemistry Letters , pp. 407
    • Nakatsuka1    Miyazaki2    Goto3
  • 11
    • 84919014171 scopus 로고    scopus 로고
    • 1H NMR and mass spectral properties. Yields have not been optimized in any of the reaction steps.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.