[2+2] Cycloadditions by Oxidative Visible Light Photocatalysis

Title[2+2] Cycloadditions by Oxidative Visible Light Photocatalysis
Publication TypeJournal Article
Year of Publication2010
AuthorsIschay, MA, Lu, Z, Yoon, TP
JournalJournal of the American Chemical Society
Volume132
Pagination8572-+
Date PublishedJun
Accession NumberISI:000279196500020
Keywordsaromatic enamines, catalysis, cation-radicals, Chemistry, Multidisciplinary, diels-alder, electron-transfer reactions, energy-conversion, METAL-COMPLEXES, organic-synthesis, radical pericyclic-reactions, Solar-energy
Abstract

Photochemical reactions are remarkable for their ability to easily assemble cyclobutanes and other strained ring systems that are difficult to construct using other conventional synthetic methods. We have previously shown that Ru(bpy)(3)(2+) is an efficient photocatalyst that promotes the [2+2] cycloadditions of electron-deficient olefins with visible light. Here, we show that Ru(bpy)(3)(2+) is also an effective photocatalyst for the [2+2] cycloaddition of electron-rich olefins. This transformation is enabled by the versatile photoelectrochemical properties of Ru(bpy)(3)(2+), which enables either one-electron reduction or one-electron oxidation of interesting organic substrates under appropriate conditions.

Short TitleJ. Am. Chem. Soc.