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ChemInform 2012, 43, issue 01 © 2012 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim Carbonylation O 0305 DOI: 10.1002/chin.201201039 Palladium-Catalyzed Regioselective Aerobic Oxidative C—H/N—H Carbonyla- tion of Heteroarenes under Base-Free Conditions. — Using air as oxidant and a bal- loon pressure of CO, indoles, thiophenes and benzothiophenes are converted in the presence of different alcohols into carboxylic acid esters. The reaction proceeds with high regioselectivity for each type of heterocycle. — (ZHANG, H.; LIU, D.; CHEN, C.; LIU, C.; LEI*, A.; Chem. Eur. J. 17 (2011) 35, 9581-9585, http://dx.doi.org/10.1002/chem.201101300 ; Coll. Chem. Mol. Sci., Wuhan Univ., Wuhan, Hubei 430072, Peop. Rep. China; Eng.) — Klein 01- 039

ChemInform Abstract: Palladium-Catalyzed Regioselective Aerobic Oxidative C—H/N—H Carbonylation of Heteroarenes under Base-Free Conditions

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Page 1: ChemInform Abstract: Palladium-Catalyzed Regioselective Aerobic Oxidative C—H/N—H Carbonylation of Heteroarenes under Base-Free Conditions

CarbonylationO 0305 DOI: 10.1002/chin.201201039

Palladium-Catalyzed Regioselective Aerobic Oxidative C—H/N—H Carbonyla-tion of Heteroarenes under Base-Free Conditions. — Using air as oxidant and a bal-loon pressure of CO, indoles, thiophenes and benzothiophenes are converted in the presence of different alcohols into carboxylic acid esters. The reaction proceeds with high regioselectivity for each type of heterocycle. — (ZHANG, H.; LIU, D.; CHEN, C.; LIU, C.; LEI*, A.; Chem. Eur. J. 17 (2011) 35, 9581-9585, http://dx.doi.org/10.1002/chem.201101300 ; Coll. Chem. Mol. Sci., Wuhan Univ., Wuhan, Hubei 430072, Peop. Rep. China; Eng.) — Klein

01- 039

ChemInform 2012, 43, issue 01 © 2012 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim

Page 2: ChemInform Abstract: Palladium-Catalyzed Regioselective Aerobic Oxidative C—H/N—H Carbonylation of Heteroarenes under Base-Free Conditions

ChemInform 2012, 43, issue 01 © 2012 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim