Palladium-Catalyzed Oxidative CH Bond Acylation of Acetanilides with Benzylic Alcohols
作者:Yu Yuan、Duanteng Chen、Xiaowei Wang
DOI:10.1002/adsc.201100417
日期:2011.12
An efficient and clean method to construct CC bonds has been developed via the acylation reaction of acetanilides with benzylic alcohols using tert-butyl hydroperoxide (TBHP) as oxidant catalyzed by palladium acetate in the presence of triflic acid (TfOH). The acylation reactions exhibit excellent reactivities, and up to 95% yield of the corresponding aryl ketone could be obtained under the optimal
Palladium-catalyzed dehydrogenative coupling reactions between acetanilides and benzylicalcohols under aqueous conditions are reported. A wide range of benzophenone derivatives could be obtained in good to excellent yields up to 98 %. Mechanism studies showed that a bimetallic palladium cyclopalladated complex might be involved in the catalysis.
The para orientation by the carbonyl groups in the bromination of phenanthrenequinone derivatives has been explained on the basis of an excited state resulting from thermal excitation of the quinone and/or from a n→π* transition of the nonbonding electrons of the oxygen atoms. A general preparative method for the syntheses of 3-bromophenanthrenequinone derivatives has been developed. The structure
Palladium-Catalyzed Direct <i>ortho</i>-Acylation through an Oxidative Coupling of Acetanilides with Toluene Derivatives
作者:Zhangwei Yin、Peipei Sun
DOI:10.1021/jo302125h
日期:2012.12.21
A facile ortho-acylation of acetanilides by a Pd-catalyzed oxidative C–H activation was developed in which low toxic, stable, and commercially available toluene derivatives were first used as acylation reagents by a tandem reaction to form o-acylacetanilides with moderate to good yields. Inexpensive, safe, and environmentally benign TBHP was proved to be an effective oxidant for these transformations
Merging Photoredox with Palladium Catalysis: Decarboxylative <i>ortho</i>-Acylation of Acetanilides with α-Oxocarboxylic Acids under Mild Reaction Conditions
作者:Chao Zhou、Pinhua Li、Xianjin Zhu、Lei Wang
DOI:10.1021/acs.orglett.5b03192
日期:2015.12.18
temperature decarboxylative ortho-acylation of acetanilides with α-oxocarboxylic acids has been developed via a novel Eosin Y with Pd dual catalytic system. This dual catalytic reaction shows a broad substrate scope and good functional group tolerance, and an array of ortho-acylacetanilides can be afforded in high yields under mild conditions.