Push–pull alkenes, which bear electron-donating and-accepting group (s) at both termini of
a C C double bond, respectively, are of interest not only for their unique electronic …

Oxadiazoles experienced an almost 80-year long period of scientific lethargy before they
tickled the curiosity of chemists. The study of chemical and photochemical reactivity of 1, 2, 4 …

The N-heterocyclic carbene (NHC)-organocatalyzed [3+ 3] annulation of 2-bromoenals with
β-oxodithioesters resulting in the enantioselective synthesis of dihydrothiopyranones is …

An operationally simple and efficient domino etiquette has been developed for the facile
construction of 1, 2-dithioles employing easily accessible dithioesters as a three-atom CCS …

A metal-and oxidant-free photoinduced strategy for thioxo sulfur-selective
trifluoromethylation of β-ketodithioesters at room temperature is reported. Excellent Z/E …

β-Ketothioamides (KTAs) are versatile building blocks for the rapid construction of various
heterocyclic compounds. In the past decade, a number of successful reactions based on …

An operationally simple and user-friendly new protocol for the synthesis of 3, 5-disubstituted/
annulated isothiazoles is devised utilizing β-ketodithioesters/β-ketothioamides and NH4OAc …

An efficient, convenient and environmentally benign procedure for the synthesis of novel 1, 2-
dihydrobenzo [a] furo [2, 3-c] phenazine derivatives with high diastereoselectivity has been …

A DABCO-promoted three-component reaction of β-ketothioamides (KTAs), arylglyoxals and
2-cyanoacetates to construct disulfides tethered pyrroles by using air as an oxidant has …

A chemoselective route to thiazolines and thiazines has been devised by heterocyclization
of viable α‐N‐hydroxyimino‐β‐oxodithioesters with 2‐chloroethylamine hydrochloride/3 …