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Volumn 46, Issue 46, 2005, Pages 7977-7979

Studies on isocyanides. A facile synthesis of 4,5-dihydro-1,4- benzothiazepin-3(2H)-ones via post-condensation modifications of the Ugi reaction

Author keywords

1,4 Benzothiazepinones; Aromatic nucleophilic substitution; Isocyanides; Ugi reaction

Indexed keywords

BENZOTHIAZEPINE DERIVATIVE; CYANIDE;

EID: 26844517457     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2005.09.071     Document Type: Article
Times cited : (28)

References (22)
  • 8
    • 4243307379 scopus 로고    scopus 로고
    • Chem. Abstr. 125 1996 168038s
    • (1996) Chem. Abstr. , vol.125
  • 18
    • 26844548192 scopus 로고    scopus 로고
    • note
    • 5 (516.37): C, 58.15; H, 4.49; N, 8.14. Found: C, 58.37; H, 4.60; N, 7.86. Detailed experimental procedures, physical, analytical, and spectral data of compounds 7b-k are reported in the Supplementary data.
  • 19
    • 26844439421 scopus 로고    scopus 로고
    • note
    • 5S (477.53): C, 62.88; H, 4.85; N, 8.80. Found: C, 62.61; H, 4.96; N, 8.99. Detailed experimental procedures, physical, analytical, and spectral data of compounds 9b-k are reported in the Supplementary data.
  • 20
    • 0035939470 scopus 로고    scopus 로고
    • The formation of the internal nucleophile represents the key step in this synthesis. From this point of view the present methodology is substantially analogous to those described by Hulme and Zhu groups: P. Tempest, V. Ma, M.G. Kelly, W. Jones, and C. Hulme Tetrahedron Lett. 42 2001 4963 4966
    • (2001) Tetrahedron Lett. , vol.42 , pp. 4963-4966
    • Tempest, P.1    Ma, V.2    Kelly, M.G.3    Jones, W.4    Hulme, C.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.