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Volumn 18, Issue 37, 2012, Pages 11555-11559

The gomberg-bachmann reaction for the arylation of anilines with aryl diazotates

Author keywords

anilines; aryl diazotates; biaryls; Gomberg Bachmann reaction; radical reactions

Indexed keywords

ARYL DIAZOTATES; ARYLATIONS; BASIC CONDITIONS; BIARYLS; GOMBERG-BACHMANN REACTION; RADICAL REACTIONS; REACTION UNDER; SIDE REACTIONS; SODIUM HYDROXIDES;

EID: 84865733661     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201200430     Document Type: Article
Times cited : (59)

References (84)
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    • Reaction conditions used as described in the following articles (Gomberg-Bachmann reaction)
    • Reaction conditions used as described in the following articles (Gomberg-Bachmann reaction)
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    • Increasing reaction temperatures lead to a continuous decrease of triazene formation [ratio aminobiphenyl 12 /1,3-di(4'-chlorophenyl)triazene=4:1 (at 50 °C) and 11:1 (at 110°C)]
    • Increasing reaction temperatures lead to a continuous decrease of triazene formation [ratio aminobiphenyl 12 /1,3-di(4'-chlorophenyl)triazene=4:1 (at 50 °C) and 11:1 (at 110 °C)].
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    • nonpolar solvents diazo anhydrides 4 preferentially decompose in a homolytic fashion (see Scheme 1) and in polar solvents preferentially by ionic mechanisms (see reference [33]). For the unique reactivity of polar aryl radicals, see
    • In nonpolar solvents diazo anhydrides 4 preferentially decompose in a homolytic fashion (see Scheme 1) and in polar solvents preferentially by ionic mechanisms (see reference [33]). For the unique reactivity of polar aryl radicals, see:, G. Pratsch, C. A. Anger, K. Ritter, M. R. Heinrich, Chem. Eur. J. 2011, 17, 4104-4108.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.