Carbo-and heterocycles are widely found in natural products, biologically active structures,
medicinally relevant compounds, and in many other fine chemicals. The development of …

Ring‐fused polycyclic structures widely exist in a myriad of natural products and
pharmaceutical molecules. Consequently, the construction of such structures from readily …

An effective and simple visible light-induced heterogeneous g-C3N4-catalyzed
decarboxylative reaction of quinoxalin-2 (1 H)-ones with N-aryl glycines was developed …

The 1, n-enyne annulation reaction has emerged as one of the most powerful and
straightforward tools to build carbo-and hetero-cyclic frameworks that are found in numerous …

A photocatalytic cascade cyclization of 1, 7-enynes with acyl chlorides has been
established. This method offers an operationally simple access to diverse fused pyran …

The emergence of radical chemistry has driven chemists to develop general and efficient
radical reactions as well as to discover safe and cost‐effective radical sources. Among the …

Abstract 1, n-Enynes are a versatile class of unsaturated hydrocarbons that find broad
applications in the synthetic community of natural products, biologically active structures and …

Compared to the widely used carbon-centered radicals, N-radicals have been relatively
unexplored owing to the lack of practical and convenient production methods. Over the past …

A NiCl2-promoted [2+ 2+ 1] carboannulation of 1, 7-enynes with internally oxidative
cyclobutanone oximes to produce canyo-functionalized 4 H-cyclopenta [c] quinolin-4-ones is …

A new copper-catalyzed tandem C–H oxidative radical functionalization and annulation of
aniline-linked 1, 7-enynes with alkyl nitriles or acetone is described. This reaction allows the …