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Formal Direct Cross-Coupling of Phenols with Amines.
Chen, Zhengwang; Zeng, Huiying; Girard, Simon A; Wang, Feng; Chen, Ning; Li, Chao-Jun.
Afiliação
  • Chen Z; Department of Chemistry and FQRNT Centre for Green Chemistry and Catalysis, McGill University, 801 Sherbrooke St. W., Montreal, Quebec H3A 0B8 (Canada).
  • Zeng H; School of Chemistry and Chemical Engineering, Gannan Normal University, Ganzhou 341000 (PR China).
  • Girard SA; Department of Chemistry and FQRNT Centre for Green Chemistry and Catalysis, McGill University, 801 Sherbrooke St. W., Montreal, Quebec H3A 0B8 (Canada).
  • Wang F; Department of Chemistry and FQRNT Centre for Green Chemistry and Catalysis, McGill University, 801 Sherbrooke St. W., Montreal, Quebec H3A 0B8 (Canada).
  • Chen N; Department of Chemistry and FQRNT Centre for Green Chemistry and Catalysis, McGill University, 801 Sherbrooke St. W., Montreal, Quebec H3A 0B8 (Canada).
  • Li CJ; Department of Chemistry and FQRNT Centre for Green Chemistry and Catalysis, McGill University, 801 Sherbrooke St. W., Montreal, Quebec H3A 0B8 (Canada).
Angew Chem Int Ed Engl ; 54(48): 14487-91, 2015 Nov 23.
Article em En | MEDLINE | ID: mdl-26531683
ABSTRACT
The transition-metal-catalyzed amination of aryl halides has been the most powerful method for the formation of aryl amines over the past decades. Phenols are regarded as ideal alternatives to aryl halides as coupling partners in cross-couplings. An efficient palladium-catalyzed formal cross-coupling of phenols with various amines and anilines has now been developed. A variety of substituted phenols were compatible with the standard reaction conditions. Secondary and tertiary aryl amines could thus be synthesized in moderate to excellent yields.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2015 Tipo de documento: Article