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Volumn 45, Issue 17, 2004, Pages 3481-3484

A formal synthesis of martinelline via a combination of two types of radical reactions

Author keywords

Martinelline; Oxime ether; Pyrrolo 3,2 c quinoline; Radical reaction

Indexed keywords

HYDROGEN; MARTINELLINE;

EID: 1842637269     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2004.02.153     Document Type: Article
Times cited : (42)

References (30)
  • 22
    • 57249084541 scopus 로고    scopus 로고
    • For a review of radical translocation reactions, see:
    • For a review of radical translocation reactions, see: Robertson J., Pillai J., Lush R.K. Chem. Soc. Rev. 30:2001;94-103.
    • (2001) Chem. Soc. Rev. , vol.30 , pp. 94-103
    • Robertson, J.1    Pillai, J.2    Lush, R.K.3
  • 23
    • 0025284005 scopus 로고
    • For examples of substitution at α-carbon adjacent to nitrogen via 1,5-hydrogen atom translocation, see:
    • For examples of substitution at α-carbon adjacent to nitrogen via 1,5-hydrogen atom translocation, see: Snieckus V., Cuevas J.-C., Sloan C.P., Liu H., Curran D.P. J. Am. Chem. Soc. 112:1990;896-898.
    • (1990) J. Am. Chem. Soc. , vol.112 , pp. 896-898
    • Snieckus, V.1    Cuevas, J.-C.2    Sloan, C.P.3    Liu, H.4    Curran, D.P.5
  • 28
    • 1842778789 scopus 로고    scopus 로고
    • note
    • 9b.
  • 30
    • 0037163331 scopus 로고    scopus 로고
    • A similar conversion of the N-Ts group into the N-acyl group under Friedel-Crafts reaction conditions has been reported:
    • A similar conversion of the N-Ts group into the N-acyl group under Friedel-Crafts reaction conditions has been reported: Jiang Y., Ma D. Tetrahedron Lett. 43:2002;7013-7015.
    • (2002) Tetrahedron Lett. , vol.43 , pp. 7013-7015
    • Jiang, Y.1    Ma, D.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.