The Institute for Advanced Studies, Wuhan University, 430072, Wuhan, P. R. China.
College of Chemistry and Molecular Sciences, Wuhan University, 430072, Wuhan, P. R. China.
Angew Chem Int Ed Engl. 2020 May 18;59(21):7990-8003. doi: 10.1002/anie.201913382. Epub 2020 Feb 25.
The direct difunctionalization of alkenes, a cheap and abundant feedstock, represents one of the most attractive strategies for increasing molecular complexity in synthetic organic chemistry. In contrast with the 1,2-difunctionalization of alkenes, recent advances showcase alkene 1,n-difunctionalizations (n≠2) involving metal migration is an emerging and rapidly growing area of research. This promising strategy not only opens a novel avenue for future development of alkene transformations, but also significantly expands upon the bond disconnections available in modern organic synthesis. This Minireview summarizes recent progress in the migratory difunctionalization of alkenes, with an emphasis on the driving force for metal migration.
烯烃的直接双官能化反应,作为一种廉价且丰富的原料,代表了在合成有机化学中增加分子复杂性的最有吸引力的策略之一。与烯烃的 1,2-双官能化反应相反,最近的进展展示了涉及金属迁移的烯烃 1,n-双官能化反应(n≠2)是一个新兴且快速发展的研究领域。这种很有前途的策略不仅为烯烃转化的未来发展开辟了新途径,而且还大大扩展了现代有机合成中可用的键切断方式。本综述总结了烯烃迁移双官能化反应的最新进展,重点介绍了金属迁移的驱动力。