1
ChemInform 2011, 42, issue 42 © 2011 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim Carboxylic amides Q 0490 DOI: 10.1002/chin.201142067 Pd(II)-Catalyzed Decarboxylative Cross-Coupling of Oxamic Acids with Potassi- um Phenyltrifluoroborates under Mild Conditions. — The decarboxylative cross-coupling of oxalate (II) with (phenyl)trifluoroborate (I) leads to methyl benzoate (III). The analogous reaction of oxamic acids (IV) and (VI) with (aryl)trifluoroborates gives rise to corresponding N-mono- and N,N-disubstituted benzamides. — (LI, M.; WANG, C.; FANG, P.; GE*, H.; Chem. Commun. (Cambridge) 47 (2011) 23, 6587-6589, http://dx.doi.org/10.1039/c1cc11635e ; Dep. Chem. Chem. Biol., Indiana Univ.- Purdue Univ., Indianapolis, IN 46202, USA; Eng.) — R. Staver 42- 067

ChemInform Abstract: Pd(II)-Catalyzed Decarboxylative Cross-Coupling of Oxamic Acids with Potassium Phenyltrifluoroborates under Mild Conditions

Embed Size (px)

Citation preview

Page 1: ChemInform Abstract: Pd(II)-Catalyzed Decarboxylative Cross-Coupling of Oxamic Acids with Potassium Phenyltrifluoroborates under Mild Conditions

Carboxylic amidesQ 0490 DOI: 10.1002/chin.201142067

Pd(II)-Catalyzed Decarboxylative Cross-Coupling of Oxamic Acids with Potassi-um Phenyltrifluoroborates under Mild Conditions. — The decarboxylative cross-coupling of oxalate (II) with (phenyl)trifluoroborate (I) leads to methyl benzoate (III). The analogous reaction of oxamic acids (IV) and (VI) with (aryl)trifluoroborates gives rise to corresponding N-mono- and N,N-disubstituted benzamides. — (LI, M.; WANG, C.; FANG, P.; GE*, H.; Chem. Commun. (Cambridge) 47 (2011) 23, 6587-6589, http://dx.doi.org/10.1039/c1cc11635e ; Dep. Chem. Chem. Biol., Indiana Univ.- Purdue Univ., Indianapolis, IN 46202, USA; Eng.) — R. Staver

42- 067

ChemInform 2011, 42, issue 42 © 2011 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim