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缺电子苯乙烯的有机光催化[2+2]环加成反应。

Organophotocatalytic [2+2] Cycloaddition of Electron-Deficient Styrenes.

机构信息

Institut für Organische und Biomolekulare Chemie, Georg-August-Universität Göttingen, Tammannstraße 2, 37077, Göttingen, Germany.

University of Ioannina, Department of Chemistry, Section of Organic Chemistry and Biochemistry, 45110, Ioannina, Greece.

出版信息

Chemistry. 2023 Jan 12;29(3):e202202373. doi: 10.1002/chem.202202373. Epub 2022 Nov 27.

Abstract

A visible-light organophotocatalytic [2+2] cycloaddition of electron-deficient styrenes is described. Photocatalytic [2+2] cycloadditions are typically performed with electron-rich styrene derivatives or α,β-unsaturated carbonyl compounds, and with transition-metal-based catalysts. We have discovered that an organic cyanoarene photocatalyst is able to deliver high-value cyclobutane products bearing electron-deficient aryl substituents in good yields. A range of electron-deficient substituents are tolerated, and both homodimerisations and intramolecular [2+2] cycloadditions to fused bicyclic systems are available by using this methodology.

摘要

本文描述了可见光源引发的缺电子苯乙烯的[2+2]环加成反应。光催化[2+2]环加成反应通常使用富电子的苯乙烯衍生物或α,β-不饱和羰基化合物,并采用过渡金属催化剂。我们发现,有机氰基芳烃光催化剂能够以高产率提供带有缺电子芳基取代基的高价值环丁烷产物。该方法可以容忍多种缺电子取代基,并且可以通过该方法进行同二聚化以及稠合双环体系的分子内[2+2]环加成反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d4c/10100360/6471f0756d94/CHEM-29-0-g003.jpg

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