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Volumn 59, Issue 23, 2003, Pages 4201-4207

Samarium diiodide promoted formation of 1,2-diketones and 1-acylamido-2-substituted benzimidazoles from N-acylbenzotriazoles

Author keywords

1,2 diketones; 1 acylamido 2 alkyl (or aryl) benzimidazoles; N acylbenzotriazoles; Samarium (II) diiodide

Indexed keywords

1,2 BIS(2 FURYL) 1,2 ETHANEDIONE; 1,2 BIS(2 METHOXYPHENYL) 1,2 ETHANEDIONE; 1,2 BIS(3 CHLOROPHENYL) 1,2 ETHANEDIONE; 1,2 BIS(4 BROMOPHENYL) 1,2 ETHANEDIONE; 1,2 BIS(4 CHLOROPHENYL) 1,2 ETHANEDIONE; 1,2 BIS(4 DIETHYLAMINOPHENYL) 1,2 ETHANEDIONE; 1,2 BIS(4 IODOPHENYL) 1,2 ETHANEDIONE; 1,2 BIS(4 METHYLPHENYL) 1,2 ETHANEDIONE; 1,2 BISPHENYL 1,2 ETHANEDIONE; 1H 1,2,3 BENZOTRIAZOL 1 YL(2 CHLOROPHENYL)METHANONE; 1H 1,2,3 BENZOTRIAZOL 1 YL(4 BROMOPHENYL)METHANONE; 1H 1,2,3 BENZOTRIAZOL 1 YL(4 IODOPHENYL)METHANONE; 1H 1,2,3 BENZOTRIAZOL 1 YL(4 METHOXYPHENYL)METHANONE; 1H 1,2,3 BENZOTRIAZOL 1 YL(HEXYL)METHANONE; 1H 1,2,3 BENZOTRIAZOL 1 YL(NONYL)METHANONE; 1H 1,2,3 BENZOTRIAZOL 1 YL(OCTYL)METHANONE; BENZIMIDAZOLE DERIVATIVE; BENZOTRIAZOLE DERIVATIVE; KETONE DERIVATIVE; SAMARIUM DIIODIDE; UNCLASSIFIED DRUG;

EID: 0038734278     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(03)00575-1     Document Type: Article
Times cited : (37)

References (43)
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    • · radical, which is known for its rapid decarbonylation. See: (a) Lunazzi L., Ingold K.U., Scalano J.C. J. Phys. Chem. 87:1983;529 (b) Turro N.J., Gold I.R., Baretz B.H. J. Phys. Chem. 87:1983;531.
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    • · radical, which is known for its rapid decarbonylation. See: (a)
    • · radical, which is known for its rapid decarbonylation. See: (a) Lunazzi L., Ingold K.U., Scalano J.C. J. Phys. Chem. 87:1983;529 (b) Turro N.J., Gold I.R., Baretz B.H. J. Phys. Chem. 87:1983;531.
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    • N-Acylbenzotriazoles are efficient acylating agents which have been used in the preparation of amides. See:
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    • 2 is based on our previous work: (a)
    • The formation of intermediate D to product 2 is based on our previous work: (a) Zhou L.H., Zhang Y.M. J. Chem. Soc. Perkin. Trans. 1. 1998;2899 (b) Zhong W.H., Chen Y.Y., Zhang Y.M. J. Chem. Res.(S). 2000;292.
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    • The formation of intermediate D to product 2 is based on our previous work: (a) Zhou L.H., Zhang Y.M. J. Chem. Soc. Perkin. Trans. 1. 1998;2899 (b) Zhong W.H., Chen Y.Y., Zhang Y.M. J. Chem. Res.(S). 2000;292.
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    • The formation of intermediate
    • The formation of intermediate D to product 2 is based on our previous work: (a) Zhou L.H., Zhang Y.M. J. Chem. Soc. Perkin. Trans. 1. 1998;2899 (b) Zhong W.H., Chen Y.Y., Zhang Y.M. J. Chem. Res.(S). 2000;292.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.