Preparation and Properties of N,N,N',N'-Tetrasubstituted 1,4-Benzenediamines.
摘要:
The synthesis of nine different N,N,N',N'-tetrasubstituted 1,4-benzenediamines is described. These compounds are of interest as mediators for glucose oxidase based biosensors and as donor molecules for conducting molecular solids. The electrochemical behaviour and the electronic absorption spectra have been investigated.
A highly efficient precatalyst for amination of aryl chlorides: synthesis, structure and application of a robust acenaphthoimidazolylidene palladium complex
作者:Tao Tu、Weiwei Fang、Jian Jiang
DOI:10.1039/c1cc15503b
日期:——
A robust palladium NHC complex was synthesized and exhibits exceptional activity and selectivity as a precatalyst in the amination of aryl chlorides and tolerates a wide range of substrates at low catalyst loadings.
Palladium-Catalyzed Amination of Aryl Sulfides with Aliphatic Amines
作者:Ke Gao、Hideki Yorimitsu、Atsuhiro Osuka
DOI:10.1002/ejoc.201500226
日期:2015.4
Conditions for the palladium–NHC-catalyzed amination of arylsulfides with aliphatic as well as aromatic amines were established. The KHMDS-mediated amination of heteroaryl sulfides could proceed without palladium. Based on the distinct difference in reactivity of C–Br and C–S bonds, a sequential amination of bromothioanisole can take place to install two different alkylamino groups onto the aromatic
Novel robust benzimidazolylidene palladium complexes: synthesis, structure, and catalytic applications in amination of chloroarenes
作者:Weiwei Fang、Jian Jiang、Yong Xu、Juefei Zhou、Tao Tu
DOI:10.1016/j.tet.2012.11.003
日期:2013.1
A series of novel pyridine stabilized Pd-NHC complexes were developed, which revealed high activities and broad substrates tolerance in the amination of various (hetero)-aryl chlorides. Besides various secondary amines, a wide range of primary anilines and aliphatic amines were also well tolerated. The results highlight us a new strategy to increase catalyst activity in the future catalyst design by alternating the sigma-donor property and flexibility of NHC ligands. (C) 2012 Elsevier Ltd. All rights reserved.
Buchwald–Hartwig Amination of (Hetero)Aryl Tosylates Using a Well-Defined N-Heterocyclic Carbene/Palladium(II) Precatalyst
作者:Yin Zhang、Guy Lavigne、Vincent César
DOI:10.1021/acs.joc.5b01272
日期:2015.8.7
The cross-coupling of aryl tosylates with amines and anilines was achieved by using for the first time a Pd-NHC system based on the popular Pd-PEPPSI precatalyst platform in which the anchoring imidazol-2-ylidene ligand IPr(Nme2)2 incorporates two dimethylamino groups as backbone substituents enhancing both the electronic and steric properties of the carbene. The system optimization and its application scope are disclosed.
USE OF BENZENE DERIVATIVES AS CHARGE TRANSFER MEDIATORS