Acknowledgement We are grateful for support of this project by the National Natural Science Foundation of China (No. J1103307) and the project of Science Foundation of Gansu Province (No. 1208RJZA266).
A novel and efficient approach to the synthesis of 2-substituted benzimidazoles has been developed via CuI/DMEDA-catalyzed coupling reaction and post-cyclization with glacial acetic acid from readily available 2-iodoa...
A direct and efficient approach to 1-aminoindolizines through three-component one-pot reaction of heteroaryl aldehydes, secondary amines and terminal alkynes catalyzed by CuI under solvent-free conditions has been dev...
This work was supported by the National Natural Science Foundation of China (No. 20802049).
A simple and efficient C--N cross-coupling method of aryl halides with various heterocycles was reported, by using 10 tool% of CuI as catalyst and 1.2 equiv. Nail as base. Aryl iodides, aryl bromides and many substitu...
Project supported by the National Natural Science Foundation of China (Nos. 20332020, 20472079).
In this article, a general, simple, and inexpensive catalyst system was developed for the amidation of aryl bromide by using CuI as catalyst, amino acid as ligand, and K3PO4 as base.
ProjectsupportedbytheNationalNaturalScienceFoundationofChina (No .2 0 2 710 3 6) ,theNaturalScienceFoundationoftheEducationCommitteeofJiangsuProvince (No .0 2KJB15 0 0 0 1) ,StateKeyLabofCoordinationChemistryofNanjingUniversity ,andtheScientificResearchF
Reaction of [PPh_4][(η 5-C_5Me_5)WS_3] with CuI,CuBr and bis^(diphenylphosphino)methane (dppm) (molar ratio=1∶2∶1∶1) in MeCN gave rise to [PPh_4][(η 5-C_5Me_5)WS_3(CuBr)(CuI)_2-(μ-dppm)] (1) in high yield. Com...