过渡金属催化的硫酯的交叉偶联反应研究进展
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韩明亮, 2018年博士毕业于南开大学, 获有机化学博士学位. 2019年至2021年在上海药物所(和深圳大学合作)从事博士后研究, 2021年进入浙江大学(和杭州中美华东制药有限公司合作)从事博士后研究. 主要从事功能性有机小分子化合物的设计、合成, 以及过渡金属催化的硫酯的有机合成方法研究. |
收稿日期: 2023-01-17
网络出版日期: 2023-03-03
Progress on the Transition Metal-catalyzed Cross-coupling Reaction of Thioesters
Received date: 2023-01-17
Online published: 2023-03-03
硫酯在医药、农药、香精香料、材料等领域应用广泛, 可从羧酸衍生得到, 羧酸在自然界寻常可见、结构丰富. 硫酯C(O)—S键能轻易和低价过渡金属发生氧化加成生成C(O)—M—S, 该物种在不脱羰或脱羰情况下可以和亲核试剂反应构建碳碳键. 近二十年来, 人们广泛研究了过渡金属催化的硫酯的交叉偶联反应, 这为从羧酸出发构筑C—C键提供了可供选择的有效方案. 本综述按照过渡金属种类, 依次对钯、镍、铜、铑等过渡金属催化的硫酯的交叉偶联反应进行了总结和讨论, 综述了该类反应在天然产物、药物分子合成及其后期转化中的应用. 同时关注了近些年报道的硫酯的不对称交叉偶联反应, 以及硫酯的交叉偶联反应在串联反应和官能团转化方面的应用.
韩明亮 , 徐丽华 . 过渡金属催化的硫酯的交叉偶联反应研究进展[J]. 化学学报, 2023 , 81(4) : 381 -392 . DOI: 10.6023/A23010013
Thioesters with intriguing chemistry and reactivity are widely used in pharmaceuticals, pesticides, perfume & flavors and materials. Thioesters are versatile building blocks in organic synthesis and are also often employed as electrophilic acylating reagents in substitution reactions, such as Corey-Nicolaou macrolactonizations and native chemical ligation for peptide connection. Thioesters can be easily obtained from direct thioesterification of carboxylic acids with various thiol sources. Whereas more efforts have been made to develop new reactions employing thioesters, their application in organic synthesis is rare compared with other carboxylic acid derivatives. Transition-metal-catalyzed C—S bond activation paves a new avenue to exploit thioester. Many new transformations have been developed, including reduction to aldehydes, decarbonylation to thioethers, addition to unsaturated bonds, and cross-coupling of thioesters with organometallic reagents. Compared with other carboxylic acid derivatives, thioesters are stable but reactive and could undergo the oxidative addition of C(O)—S to low-valent transition-metal species, generating the C(O)—M—S. Transition-metal-catalyzed cross-coupling reaction of thioesters have been extensively studied in the last two decades, and providing alternative and efficient ways to construct C—C bonds. Despite the reaction between thioester and selected organometallic reagents to furnish ketones, thioesters could also be employed as decarbonylative coupling electrophiles. The advances in transition-metal-catalyzed cross-coupling reaction of thioesters are summarized in this review, which is presented by the categories of transition metals including Pd, Ni, Cu and Rh. Simultaneously, synthetic applications of transition-metal-catalyzed cross-coupling reaction of thioesters in nature products and pharmaceuticals are discussed. Attention is also paid to the asymmetric cross-coupling reaction of thioesters reported in recent years, the application of cross-coupling reaction of thioesters in tandem reactions and functional group transformations.
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