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Volumn 59, Issue 26, 2003, Pages 4767-4774

Application of directed metalation in synthesis. Part 4: Expedient synthesis of substituted benzo[b]thiophene and naphthothiophene

Author keywords

Benzo b thiophene; Directed metalation; Intramolecular cyclisation; Naphthothiophene; Thioindoxyl

Indexed keywords

2,3 DIHYDRO 3 HYDROXY 4 CHLOROBENZO[B]THIOPHENE; 2,3 DIHYDRO 4 CHLOROBENZO[B]THIOPHEN 3 ONE; 2,3 DIHYDRO 4 METHOXYBENZO[B]THIOPHEN 3 ONE; 2,3 DIHYDRO 4 METHOXYNAPHTHO[1,2 B]THIOPHEN 3 ONE; 2,3 DIHYDRO 4 METHYLSULFANYLBENZO[B]THIOPHEN 3 ONE; 2,3 DIHYDRO 4 TRIMETHYLSILYL 5 METHOXYBENZO[B]THIOPHEN 3 ONE; 2,3 DIHYDRO 4,5 DIMETHOXYBENZO[B]THIOPHEN 3 ONE; 2,3 DIHYDRO 4,6 DIMETHOXYBENZO[B]THIOPHEN 3 ONE; 2,3 DIHYDRO 5 METHOXYSULFANYLBENZO[B]THIOPHEN 3 ONE; 2,3 DIHYDRO 6 METHOXYBENZO[B]THIOPHEN 3 ONE; 2,3 DIHYDRO 6 METHYLBENZO[B]THIOPHEN 3 ONE; 2,3 DIHYDRO 7 METHOXYBENZO[B]THIOPHEN 3 ONE; 4 METHOXYBENZO[B]THIOPHENE; 4 METHYLSULFANYLBENZO[B]THIOPHENE; 4,5 DIMETHOXYBENZO[B]THIOPHENE; 4,6 DIMETHOXYBENZO[B]THIOPHENE; 5 METHOXYBENZO[B]THIOPHENE; 6 METHOXYBENZO[B]THIOPHENE; 6 METHYLBENZO[B]THIOPHENE; 7 METHOXYBENZO[B]THIOPHENE; BENZAMIDE DERIVATIVE; BENZOTHIOPHENE DERIVATIVE; N,N DIETHYL 2 METHYLSULFANYL 3 METHOXYBENZAMIDE; N,N DIETHYL 2 METHYLSULFANYL 4 METHOXYBENZAMIDE; N,N DIETHYL 2 METHYLSULFANYL 5 METHOXY 6 TRIMETHYLSILYLBENZAMIDE; N,N DIETHYL 2 METHYLSULFANYL 5 METHOXYBENZAMIDE; N,N DIETHYL 2 METHYLSULFANYL 6 METHOXYBENZAMIDE; THIOL DERIVATIVE; THIOPHENE DERIVATIVE; UNCLASSIFIED DRUG; UNINDEXED DRUG;

EID: 0038515214     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(03)00710-5     Document Type: Article
Times cited : (34)

References (31)
  • 3
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    • For example of the utilisation of N,N-diethylcarbamoyl group in cyclisation, cf.
    • For example of the utilisation of N,N-diethylcarbamoyl group in cyclisation, cf. Ardeo A., Lete E., Sotomyer N. Tetrahedron Lett. 41:2000;5211.
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    • Ardeo, A.1    Lete, E.2    Sotomyer, N.3
  • 8
    • 0003607021 scopus 로고
    • A. Weissberger. Wiley Interscience New York (b). A.R. Katritzky, Boulton A.J. Accademic New York (c). A.R. Katritzky, Boulton S.J. Academic New York (e). A.R. Katritzky, Rees C.W. New York: Pergamon
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    • (1984) Comprehensive Heterocyclic Chemistrty , vol.4
    • Rajappa, S.1
  • 11
    • 0036351597 scopus 로고    scopus 로고
    • Use of commercially available methyl 2-methylthiobenzoate by the authors restricted them to only the parent thioindoxyl carrying no substituent in the benzene ring
    • Cabiddu M.G., Cabiddu S., Cadoni E., Montis S., Fattuoni C., Melis S., Usai M. Synthesis. 2002;875. Use of commercially available methyl 2-methylthiobenzoate by the authors restricted them to only the parent thioindoxyl carrying no substituent in the benzene ring.
    • (2002) Synthesis , pp. 875
    • Cabiddu, M.G.1    Cabiddu, S.2    Cadoni, E.3    Montis, S.4    Fattuoni, C.5    Melis, S.6    Usai, M.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.