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Volumn 128, Issue 38, 2006, Pages 12366-12367

Catalytic one-pot synthesis of cyclic amidines by virtue of tandem reactions involving intramolecular hydroamination under mild conditions

Author keywords

[No Author keywords available]

Indexed keywords

AMIDINE;

EID: 33749168701     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja064788i     Document Type: Article
Times cited : (123)

References (29)
  • 11
    • 33749173032 scopus 로고    scopus 로고
    • note
    • For details, see Supporting Information.
  • 12
    • 33749183757 scopus 로고    scopus 로고
    • note
    • N-Propyl substrate afforded a similar result compared to N-benzyl.
  • 13
    • 33749175986 scopus 로고    scopus 로고
    • note
    • No reaction was observed using internal aminoalkynes with azides.
  • 17
    • 34249764398 scopus 로고
    • Although the exact route to the enamine intermediates is not completely elucidated, one reviewer suggested a vinylidene pathway via metal actylides in addition to a pathway via the direct catalytic attack of amino group across the triple bonds. See, Sappa, E. J. Cluster Sci. 1994, 5, 211.
    • (1994) J. Cluster Sci. , vol.5 , pp. 211
    • Sappa, E.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.