A general and efficient photocatalytic annulation‐carbohalogenation of 1, 7‐enynes with a
wide variety of alkyl halides was reported, which led to the atom‐economic synthesis of …

Radical annulative carbohalofunctionalization of 1, n-enynes via atom transfer processes
constitutes an efficient and practical synthetical strategy for accessing halogenated cyclic …

A photocatalytic decarboxylative/defluorinative [4 + 3] annulation of o -hydroxyphenylacetic
acids and trifluoromethyl alkenes: synthesis of fluorinat ... - Organic Chemistry Frontiers (RSC …

A sustainable and efficient visible-light-induced Ir (III)-catalyzed annulation of 1, 7-diynes
with ICF 2 CO 2 Et is reported under mild neutral-redox conditions, furnishing a wide range …

A visible-light-induced 1, 1-hydrofluoroalkylation of alkynes with a concomitant vicinal
acylation is developed using tetrahydrofuran (THF) as the hydrogen atom source. Various …

Herein, a photocatalytic system for defluorinative [4+ 2] annulation of gem‐difluoroalkenes
with unactivated alkenes is realized. This protocol was compatible with a broad scope of …

A practical and eco-friendly strategy for the radical-mediated decarboxylative [3+ 2] and [4+
2] annulation of enynals and γ, σ-unsaturated N-(acyloxy) phthalimides through the …

Comprehensive Summary Tetralin‐1‐carboxamides are frequently incorporated in myriad
medicinally important molecules. However, their existing synthetic routes not only suffer from …

We present the first example of visible-light-mediated multicomponent annulation of 1, 7-
diynes by taking advantage of quadruple cleavage olf carbon-halogen bonds of BrCCl3 to …

One‐step syntheses of carbocycles substituted with amines from simple starting materials
remain rare. We recently developed an intermolecular [3+ 2] annulation of …