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Enantioselective Heck-Matsuda Reactions: From Curiosity to a Game-Changing Methodology
The Chemical Record ( IF 6.6 ) Pub Date : 2021-06-26 , DOI: 10.1002/tcr.202100149
Caio C Oliveira 1 , Carlos Roque Duarte Correia 1
Affiliation  

The enantioselective palladium-catalyzed Heck arylation of olefins using arenediazonium salts is one of the last features in the evolution of a synthetic method known as the Heck-Matsuda reaction. This personal account highlights the development of the enantioselective Heck-Matsuda reaction in its initial stages, the challenges faced along the way, and the interesting findings that opened new synthetic opportunities, mainly from our laboratory, featuring the Heck-Matsuda reaction as a central player in the synthesis of bioactive and functional molecules.

中文翻译:

对映选择性 Heck-Matsuda 反应:从好奇心到改变游戏规则的方法论

使用芳烃重氮盐对烯烃进行对映选择性钯催化的 Heck 芳基化反应是合成方法发展中的最后一个特征之一,称为 Heck-Matsuda 反应。这篇个人报道重点介绍了对映选择性 Heck-Matsuda 反应在其初始阶段的发展、沿途面临的挑战以及主要来自我们实验室的有趣发现,这些发现开辟了新的合成机会,其中 Heck-Matsuda 反应是核心参与者在生物活性和功能分子的合成中。
更新日期:2021-06-26
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