An important strategy for the efficient generation of diversity in molecular structures is the
utilization of common starting materials in chemodivergent transformations. The most …

Abstract The synthesis of 4‐(trifluoromethyl)‐2, 3‐dihydrothiazoles from α‐enolic dithioesters
and imidoyl sulfoxonium ylides has been achieved under thermal conditions. This …

The diversified synthesis of heterocyclic compounds has always been one of the popular
subjects of organic chemistry. To this end, great efforts have been devoted to developing …

A novel visible-light-induced photoredox-catalyzed regioselective radical cyclization
reaction of isocyanides with thioethers has been developed for the first time. This reaction …

The synthesis of two kinds of five-membered organosulfur heterocycles (ie, 1, 4, 2-
oxathiazoles and 1, 3, 4-thiadiazoles) from α-enolic dithioesters with active 1, 3-dipoles …

Acid-controlled, chemodivergent and redox-neutral annulations for the synthesis of
isocoumarins and isoquinolinones have been realized via Rh (III)-catalyzed Csingle bondH …

A concise and direct one-pot [4+ 1] synthetic strategy for the construction of 2-substituted
benzazoles such as benzoxazoles and benzothiazoles has been disclosed in high yields …

Abstract Fe 3 O 4-TDSN-Bi (III) was utilized as an efficient and reusable catalyst for the
regioselective one-pot synthesis of quinoline derivatives from arylamines, arylaldehydes …

An operationally simple cascade protocol has been developed for the construction of 1, 2-
and 1, 3-dithiole derivatives from α-enolic dithioesters. 1, 2-Dithioles are achieved by the …

An efficient Bi (OTf) 3‐catalyzed method for the synthesis of quinoline‐4‐carboxylates
through a domino cyclization/esterification reaction of isatins with enaminones in alcohols is …