Arshadi Sattar, Banaei Alireza, Monfared Aazam, Ebrahimiasl Saeideh, Hosseinian Akram
Department of Chemistry, Payame Noor University Tehran Iran.
Department of Chemistry, Ahar Branch, Islamic Azad University Ahar Iran.
RSC Adv. 2019 May 31;9(30):17101-17118. doi: 10.1039/c9ra01941c. eCollection 2019 May 29.
Transition-metal catalyzed cross-dehydrogenative-coupling reactions encompass highly versatile and atom economical methods for the construction of various carbon-carbon and carbon-heteroatom bonds by combining two C(X)-H (X = heteroatom) bonds. Along this line, direct acyloxylation of C-H bonds with carboxylic acids has emerged as a powerful and green approach for the synthesis of structurally diverse esters. In this focus-review we will describe recent progress in direct esterification of aromatic C-H bonds with special emphasis on the mechanistic features of the reactions. Literature has been surveyed until the end of February 2019.
过渡金属催化的交叉脱氢偶联反应包含高度通用且原子经济的方法,通过结合两个C(X)-H(X = 杂原子)键来构建各种碳-碳和碳-杂原子键。沿着这条路线,羧酸对C-H键的直接酰氧基化已成为合成结构多样酯的一种强大且绿色的方法。在这篇重点综述中,我们将描述芳香族C-H键直接酯化的最新进展,特别强调反应的机理特征。文献调研截止到2019年2月底。