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Volumn , Issue 16, 2008, Pages 2589-2593

Iodobenzene dichloride in combination with sodium azide for the effective synthesis of carbamoyl azides from aldehydes

Author keywords

Aldehydes; Carbamoyl azides; Hypervalent iodine; Iodobenzene dichloride; Oxidations

Indexed keywords

ACETONITRILE; ALDEHYDES; COMPLEXATION; COMPUTER NETWORKS; SODIUM; SUGAR (SUCROSE);

EID: 50849140828     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2008-1067196     Document Type: Article
Times cited : (31)

References (38)
  • 32
    • 50849129416 scopus 로고    scopus 로고
    • When n-heptanal was treated with 1.2 equiv of PhICl2 and 2.4 equiv of NaN3, the yield of hexylcarbamoyl azide decreased to 75, which was 19% lower than that with 2.0 equiv of PhICl2 and 4.0 equiv of NaN3 under the otherwise same reaction conditions Table 1, entry 5, Thus, in order to obtain the excellent outcome within the shorter time period and taking into account that both PhICl2 and NaN3 are readily available and cost-effective, 2 equiv of PhICl2 and 4 equiv of NaN3 were used in the subsequent work
    • 3 were used in the subsequent work.
  • 34
    • 0027481924 scopus 로고    scopus 로고
    • 2, see: (a) Fontana, F.; Minisci, F.; Yan, Y. M.; Zhao, L. Tetrahedron Lett. 1993, 34, 2517.
    • 2, see: (a) Fontana, F.; Minisci, F.; Yan, Y. M.; Zhao, L. Tetrahedron Lett. 1993, 34, 2517.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.