Visible light mediated azomethine ylide formation—photoredox catalyzed [3+2] cycloadditions -
Chemical Communications (RSC Publishing) DOI:10.1039/C1CC13660G Royal Society of …

Abstract Intermolecular [3+ 2] annulation of cyclopropylanilines with alkynes is realized
using visible light photoredox catalysis, yielding a variety of cyclic allylic amines in fair to …

A new oxidative [3+ 2] cycloaddition of N-substituted hydroxylamines with alkenes was
established under visible light photoredox catalysis. This novel protocol provides a rapid …

Cycloaddition reactions offer great advantages regarding atom and step economy for the
construction of various carbocycles and heterocycles. While the recent development based …

A highly regioselective [2+ 2+ 2] cyclization of aromatic alkynes with nitriles is developed for
the preparation of 2, 3, 6-trisubstituted pyridines under visible-light irradiation using a …

A novel method for the concise synthesis of cyclohepta [b] indoles in high yields was
developed. The method involves a visible‐light‐induced, photocatalyzed [2+ 2] …

A direct alkoxycarbonylation/cyclization reaction is accomplished under visible light-induced
photoredox catalysis. With this approach, a variety of ester-substituted indolo [2, 1-a] …

A visible-light photoredox synthesis of 3-acylindoles through intramolecular oxidative
cyclization of o-alkynylated N, N-dialkylamines is developed. The reaction proceeds …

We report an organophotocatalytic 1, 2-oxyalkynylation of ene-carbamates and enol ethers
using Ethynyl BenziodoXolones (EBXs). 1-Alkynyl-1, 2-amino alcohols and diols were …

A new and efficient synthesis of highly substituted tetrahydroimidazole derivatives by means
of visible light-induced intramolecular cyclization reactions has been described. This …