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Volumn 43, Issue 41, 2002, Pages 7393-7396

Pummerer reaction methodology for the synthesis of 5-thiophenyl substituted oxazoles

Author keywords

5 thiophenyloxazoles; Diazonamide A; Oxazole

Indexed keywords

BENZENE DERIVATIVE; N CHLOROSUCCINIMIDE; OXAZOLE DERIVATIVE; SUCCINIMIDE DERIVATIVE; TIN CHLORIDE; UNCLASSIFIED DRUG;

EID: 0037037837     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(02)01704-5     Document Type: Article
Times cited : (25)

References (48)
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    • for modifications by Cornforth, see: (e) Cornforth, J. W.; Cornforth, R. H. J. Chem. Soc. 1947, 96; (f) Cornforth, J. W.; Cornforth, R. H. J. Chem. Soc. 1953, 93; (g) Green, N.; LaForge, F. B. J. Am. Chem. Soc. 1948, 70, 2812.
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    • for modifications by Cornforth, see: (e) Cornforth, J. W.; Cornforth, R. H. J. Chem. Soc. 1947, 96; (f) Cornforth, J. W.; Cornforth, R. H. J. Chem. Soc. 1953, 93; (g) Green, N.; LaForge, F. B. J. Am. Chem. Soc. 1948, 70, 2812.
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    • for structural revision, see: (b) Li, J.; Jeong, S.; Esser, L.; Harran, P. G. Angew. Chem., Int. Ed. 2001, 40, 4765; © Li, J.; Burgett, A. W. G.; Esser, L.; Amezcua, C.; Harran, P. G. Angew. Chem., Int. Ed. 2001, 40, 4770.
    • (2001) Angew. Chem., Int. Ed. , vol.40 , pp. 4765
    • Li, J.1    Jeong, S.2    Esser, L.3    Harran, P.G.4
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    • +) 330.0952, found 330.0951
    • +) 330.0952, found 330.0951.
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    • +) 206.0639, found 206.0631.
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    • Desulfurization of 2-phenyl-5-thiophenyloxazole with deactivated Raney nickel in acetone gave 2-phenyloxazole (67%)
    • Desulfurization of 2-phenyl-5-thiophenyloxazole with deactivated Raney nickel in acetone gave 2-phenyloxazole (67%).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.