共查询到20条相似文献,搜索用时 46 毫秒
1.
C—N,C—O键偶联是有机合成中的一类重要反应,铜催化的偶联反应是该类化学键形成中的主要手段之一,相比钯等过渡金属,金属铜具有低毒、廉价、反应条件温和等优点.按照所形成化合物的结构类型综述了铜催化C—N,C—O键偶联反应的最新研究进展. 相似文献
2.
为设计一种利用廉价催化剂以达成C—H活化构建C—S的方法,本文研究了铜催化C—H活化/C—S偶联反应合成系列环烷基芳基硫醚化合物。以芳基磺酰肼与环烷烃为原料,溴化亚铜为催化剂,二叔丁基过氧化物(DTBP)为氧化剂,120℃反应24 h,经氧化脱氮C—H活化/C—S偶联串联反应过程,合成了系列环烷基芳基硫醚化合物。该反应适合环戊烷、环己烷、环庚烷、环辛烷和环十二烷等环烷烃和不同取代基团(甲氧基、硝基、氯和甲基)的芳基酰肼,合成得到了18个芳基硫醚类化合物,产率为41%~72%。其结构经1H NMR、13C NMR和HR-MS进行了表征。 相似文献
3.
5.
6.
7.
8.
9.
10.
11.
LUO Kexin SU Qing JU Pengyao LI Xiaodong LIU Ziqian SUN Xiaoman LI Guanghua WU Qiaolin 《高等学校化学研究》2020,36(6):1302-1309
Salen-porphyrin-based conjugated microporous polymers(CMPs) have been demonstrated to be an attractive material platform for predesigned structures and promising applications. Herein, a new salen-porphyrin-based conjugated microporous polymer(SP-CMP-L) was solvothermally prepared by porphyrin-forming condensation reaction of pyrrole and salen-dialdehyde derivative. The SP-CMP-L was characterized by spectroscopy technologies, and also exhibited excellent thermal and chemical stability. The porosity of SP-CMP-L was examined by N2 adsorption/desorption isotherms. The BET specific surface area of the CMP material was calculated to be 290.4 m2/g with the pore volume of 0.19 cm3/g. The microstructure property of the resulting material was further evaculated by scanning electron microscopy(SEM) and transmission electron microscopy(TEM). The SP-CMP-L with salen and porphyrin multidentate coordination sites was proposed to serve as an initiator to promote the cross-coupling between aryl halides with unactivated arenes under base-mediated conditions. The transition-metal-free catalytic protocol provided high catalytic activity for direct C-H arylation reaction of unactivated arenes, and thus offered a convenient and efficient alternative for the construction biaryl scaffolds. In addition, the salen-porphyrin-based CMP material possessed remarkable adsorption capability for the removal of organic amines from water. 相似文献
12.
13.
14.
15.
Hajar Baguia Prof. Gwilherm Evano 《Chemistry (Weinheim an der Bergstrasse, Germany)》2022,28(6):e202103599
An efficient and broadly applicable process is reported for the copper-catalyzed direct perfluoroalkylation of C−H bonds in heteroarenes with commercially available perfluoroalkyl iodides. This reaction is based on a simple combination of copper(I) iodide and 1,10-phenanthroline enabling the easy reduction of perfluoroalkyl iodides to the corresponding radical species that add to a wide range of heteroarenes including benzofurans, benzothiophenes, (aza)indoles, furans and pyrroles. High levels of regioselectivity were obtained in all cases and the efficiency and robustness of this process was highlighted by the direct perfluoroalkylation of furan-containing peptides. 相似文献
16.
17.
18.
Prof. Dr. Hideki Amii 《Chemical record (New York, N.Y.)》2023,23(9):e202300154
Trifluoromethylated aromatic compounds (Ar−CF3) are the substances of considerable interest in various industrial fields. The high lipophilicity, strong electron-withdrawing ability, and characteristic size of trifluoromethyl group are key influences in biologically active molecules. Due to these attractive properties, the benzotrifluoride structural motifs have been widely employed in the design of pharmaceuticals, agrochemicals, dyes, liquid crystals, and polymers. Therefore, the development of highly efficient methodologies for aromatic trifluoromethylation is of significant importance for wide fields of science and technology. Recently, a great deal of attention has been paid to catalytic protocols to introduce fluoroalkyl groups into aromatic rings selectively. This personal account highlights the copper-mediated aromatic trifluoromethylation and the related transformations developed by our research group. 相似文献
19.
[reaction: see text] A new method for the rhodium-catalyzed arylation of a variety of heterocycles has been developed. The reaction provided moderate to good yields of the arylated products. A preliminary mechanistic investigation of this reaction revealed the intermediacy of an isolable N-heterocyclic carbene complex. 相似文献
20.
Copper-Catalyzed Synthesis of Axially Chiral Biaryls with Diaryliodonium Salts as Arylation Reagents
NOBIN and BINAM derivatives harboring biaryl frameworks are recognized as a class of important atropisomers with versatile applications. Here, we present an efficient synthetic route to access such compounds through copper-catalyzed domino arylation of N-arylhydroxylamines or N-arylhydrazines with diaryliodonium salts and [3,3]-sigmatropic rearrangement. This reaction features mild conditions, good substrate compatibility, and excellent efficiency. The practicality of this protocol was further extended by the synthesis of biaryl amino alcohols. 相似文献