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Volumn 64, Issue 21, 1999, Pages 7836-7841

Radical chain reactions of α-azido-β-keto esters with tributyltin hydride. A novel entry to amides and lactams through regiospecific nitrogen insertion

Author keywords

[No Author keywords available]

Indexed keywords

BETA LACTAM DERIVATIVE; ESTER DERIVATIVE; NITROGEN; TRIBUTYLTIN;

EID: 0032695065     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo990837g     Document Type: Article
Times cited : (54)

References (42)
  • 1
    • 0004295295 scopus 로고
    • Patai, S., Ed.; Wiley Interscience: New York
    • For leading information concerning the chemistry of azides and nitrenes, see (a) The Chemistry of The Azido Group; Patai, S., Ed.; Wiley Interscience: New York, 1971.
    • (1971) The Chemistry of the Azido Group
  • 2
    • 0003525046 scopus 로고
    • Scriven, E. F. V., Ed.; Academic Press: New York
    • (b) Azides and Nilrenes-Reactivity and Utility; Scriven, E. F. V., Ed.; Academic Press: New York, 1984.
    • (1984) Azides and Nilrenes-Reactivity and Utility
  • 6
    • 33847524379 scopus 로고    scopus 로고
    • Abramovitch, R. A.; Kyba, E. P. in ref la, Ch. 5.
    • Abramovitch, R. A.; Kyba, E. P. in ref la, Ch. 5.
  • 37
    • 33847492132 scopus 로고
    • (Chem. Abstr. 1976, 84, 105797e).
    • (1976) Chem. Abstr. , vol.84
  • 38
    • 33847497519 scopus 로고    scopus 로고
    • Structural assignment to the 2-endo-bromo derivative of the keto ester 12 was fully supported by X-ray crystallographic analysis.
    • Structural assignment to the 2-endo-bromo derivative of the keto ester 12 was fully supported by X-ray crystallographic analysis.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.