A Highly Active Catalyst for Pd-Catalyzed Amination Reactions: Cross-Coupling Reactions Using Aryl Mesylates and the Highly Selective Monoarylation of Primary Amines Using Aryl Chlorides
作者:Brett P. Fors、Donald A. Watson、Mark R. Biscoe、Stephen L. Buchwald
DOI:10.1021/ja8055358
日期:2008.10.15
reactivity for C-N cross-coupling reactions is reported. This catalyst system enables the use of arylmesylates as a coupling partner in C-N bond-forming reactions. Additionally, the use of BrettPhos permits the highly selective monoarylation of an array of primary aliphatic amines and anilines at low catalyst loadings and with fast reaction times, including the first monoarylation of methylamine. Lastly
under the Pd/C-catalyzed hydrogenation conditions in the presence of diethylamine and the method could also be applicable to the hydrodeoxygenation of morphine to afford 3-deoxy-7,8-dihydromorphine. Diethylamine is not only a scavenger of the corresponding methanesulfonic acid derivative, which is produced during the reaction progress, but also a strong promoter of the Pd/C-catalyzedreduction of aryl
Addressing Challenges in Palladium-Catalyzed Cross-Couplings of Aryl Mesylates: Monoarylation of Ketones and Primary Alkyl Amines
作者:Pamela G. Alsabeh、Mark Stradiotto
DOI:10.1002/anie.201303305
日期:2013.7.8
Mor(DalPhos) for Me(sylates): Described are the first examples of ketone mono‐α‐arylation and primary aliphatic aminemonoarylation employing aryl methanesulfonate coupling partners. A range of functionalized arylmesylates were employed with dialkyl ketones, and also with primary and secondary amines as well as the otherwise challenging coupling partners acetone and methylamine. Ad=adamantyl.
Direct arylations of electron-deficient (hetero)arenes with aryl or alkenyl tosylates and mesylates
作者:Lutz Ackermann、Sabine Fenner
DOI:10.1039/c0cc02360d
日期:——
A palladium catalyst derived from the ligand X-Phos enabled generally applicable directarylations of electron-deficient heteroarenes and arenes with aryl and alkenyl tosylates or mesylates.
The present invention is a method for producing an aromatic compound by substituting the sulfonic acid group in a sulfonic acid aromatic-ester with a hydrogen atom in the presence of a platinum group metal catalyst, wherein an alkali metal carboxylate and/or an ammonium formate are made to coexist in the system. According to the present invention, an aromatic compound where the sulfonic acid group in a sulfonic acid aromatic-ester is substituted with a hydrogen atom, can be produced efficiently with good operability without using metal magnesium.