02 Apr 16:23
by Pankaj D. Rege, Andreas Schuster, Jens Lamerz, Christian Moessner, Wolfgang Göhring, Pirmin Hidber, Helmut Stahr, Oana Mihaela Andrei, Janine Burren, Alexandre Moesching, Daniel Coleman, and Stefan Hildbrand
Organic Process Research & Development
DOI: 10.1021/acs.oprd.3c00356
16 Feb 19:02
by Yusuke Imamura, Jun-ichi Ogawa, Yuma Otake, and Hidenosuke Itoh
Organic Process Research & Development
DOI: 10.1021/acs.oprd.2c00251
20 Sep 18:23
by Liang-Zhu Huang, Zi Xuan, Jong-Un Park, and Ju Hyun Kim
Organic Letters
DOI: 10.1021/acs.orglett.2c02752
20 Sep 18:23
by Peng Wu, Joachim Demaerel, Deshen Kong, Ding Ma, and Carsten Bolm
Organic Letters
DOI: 10.1021/acs.orglett.2c02804
28 Feb 20:58
by William D. Chemelewski, Heung-Chan Lee, Jung-Fu Lin, Allen J. Bard and C. Buddie Mullins
Journal of the American Chemical Society
DOI: 10.1021/ja411835a
15 Mar 13:50
by Gérard Cahiez, Alban Moyeux, Olivier Gager, Maël Poizat
Abstract
The copper-catalyzed decarboxylation of carboxylic aromatic acids has been advantageously achieved by using aliphatic amines like tetramethylethylenediamine (TMEDA) or hexamethylenetetraamine (HMTA) as ligands instead of the aromatic heterocyclic amines (quinoline, phenanthroline) used until now. The improvement is significant since the reaction can be performed at a lower temperature (ca. 50 °C less) and the reaction time is clearly shorter (15 min instead of 12 to 24 h).