Cu(OTf)2-catalyzed arylmethylation of terminal alkynes with benzylic alcohols under ligand-, base-, and additive-free reaction conditions
摘要:
An effective, convenient, and mild coupling reaction of benzylic alcohols with terminal alkynes has been developed. As an effective Lewis acid, Cu(OTF)(2)-catalyzed arylmethylation of terminal alkynes with benzylic alcohols generated the corresponding products in BrCH2CH2Br with good yields in the absence of ligand, base, and additive. (C) 2011 Elsevier Ltd. All rights reserved.
Copper-Catalyzed Cross-Dehydrogenative Coupling (CDC) of Alkynes and Benzylic CH Bonds
作者:Camille A. Correia、Chao-Jun Li
DOI:10.1002/adsc.201000066
日期:——
The activation of benzylic CH bonds and subsequent coupling with terminal alkynes in the presence of 2,3‐dichloro‐5,6‐dicyanoquinone (DDQ) and a catalyticamount of copper(I) triflate is presented. Good to moderate yields of disubstituted alkynes are obtained for this cross‐dehydrogenative coupling (CDC) reaction between a variety of aromatic alkynes and diphenylmethane derivatives.
Pd-Catalyzed Three-Component Coupling of <i>N</i>-Tosylhydrazone, Terminal Alkyne, and Aryl Halide
作者:Lei Zhou、Fei Ye、Yan Zhang、Jianbo Wang
DOI:10.1021/ja105762n
日期:2010.10.6
A Pd-catalyzed three-component reaction of N-tosylhydrazone, terminalalkyne, and aryl halide follows a mechanism involving a sequence of Pd carbene migratory insertion-transmetalation-reductive elimination, leading to the formation of one sp(2)-sp(3) C-C bond and one sp-sp(3) C-C bond.
Pd 催化的 N-甲苯磺酰腙、末端炔烃和芳基卤化物的三组分反应遵循涉及 Pd 卡宾迁移插入-金属转移-还原消除序列的机制,导致形成一个 sp(2)-sp(3) ) CC 键和一个 sp-sp(3) CC 键。
Cu(OTf)2-catalyzed arylmethylation of terminal alkynes with benzylic alcohols under ligand-, base-, and additive-free reaction conditions
作者:Kai Ren、Pinhua Li、Lei Wang、Xiuli Zhang
DOI:10.1016/j.tet.2011.02.050
日期:2011.4
An effective, convenient, and mild coupling reaction of benzylic alcohols with terminal alkynes has been developed. As an effective Lewis acid, Cu(OTF)(2)-catalyzed arylmethylation of terminal alkynes with benzylic alcohols generated the corresponding products in BrCH2CH2Br with good yields in the absence of ligand, base, and additive. (C) 2011 Elsevier Ltd. All rights reserved.