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Transition-metal-catalyzed C-S, C-Se, and C-te bond formation via cross-coupling and atom-economic addition reactions

机译:通过交叉偶联和原子经济加成反应形成过渡金属催化的C-S,C-Se和C-te键

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The state-of-the-art development of C-S, C-Se, and C-Te bond-formation research involving cross-coupling and addition reactions, are discussed. In 1998, after screening the available ligands, Zheng and coworkers found that Pd(OAc)_2-BINAP-LiCl and in particular the Pd(OAc)2-Tol- BINAP system can catalyze cross-coupling reactions of various triflates. Krief and coworkers showed that NaH or CsOH can be a more convenient choice, although the reaction may require higher temperatures. Venkataraman and co-workers suggested using neocuproin as a ligand significantly extending the scope of the reaction to include aryl(hetaryl) iodides with both electron-donating and electron-accepting substituents as well as various alkyl and aryl thiols. Wang, Wu, and co-workers reported an excellent mechanistic study of a methylacetylene bisselenation on a Pd catalyst using theoretical calculations at the B3LYP level.
机译:讨论了涉及交叉偶联和加成反应的C-S,C-Se和C-Te键形成研究的最新进展。 1998年,在筛选出可用的配体后,Zheng及其同事发现Pd(OAc)_2-BINAP-LiCl,尤其是Pd(OAc)2-Tol-BINAP系统可以催化各种三氟甲磺酸酯的交叉偶联反应。 Krief和同事表明,NaH或CsOH可能是更方便的选择,尽管反应可能需要更高的温度。 Venkataraman和同事建议使用新cuproproin作为配体,大大扩展了反应范围,使其包括具有给电子取代基和电子接受取代基的芳基(杂芳基)碘化物,以及各种烷基和芳基硫醇。 Wang,Wu和他的同事报告了在B3LYP水平上使用理论计算对Pd催化剂上的甲基乙炔双硒化进行的出色机理研究。

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