Pyridines and quinolines substituted with sulfur‐containing functional groups are widely
used as drugs, drug candidates, organic materials, N, S‐ligands and others. Traditional …

A simple, efficient, and practical method for the synthesis of S-quinolyl xanthates was
developed via Ts2O-promoted deoxygenative C–H dithiocarbonation of quinoline N-oxides …

A general, efficient and practical protocol for Ts2O promoted deoxygenative
dithiocarbamation of quinoline N-oxides with in situ generated dithiocarbamic acids from …

A convenient, efficient and practical approach for the synthesis of S-quinolyl
phosphorothioates via cheap TsCl promoted deoxygenative C2–H phosphorothiolation of …

The natural product quinine has been known to humankind for centuries, and in that time
has played a pivotal role in the treatment of malaria. Quinine, and the related cinchona …

Hydroquinine-6′-boric acid was first synthesized via a palladium-catalyzed borylation/silica
gel promoted hydrolysis sequence of hydroquinine-derived triflate and bis (pinacolato) …

A Cu (I)-catalyzed highly regioselective synthesis of 2-acetamidequinoline N-oxides using
dioxazolones with quinoline N-oxides has been reported. The reaction possesses mild …

A Lewis acid-mediated C2-N-trifluoroethylamidation of quinolines, employing quinoline N-
oxides, trifluorodiazoethane, and acetonitrile to forge a new class of N-(quinolin-2-yl)-N …

A domino reaction of o-alkenylaryl isocyanides with elemental sulfur and selenium in pure
water was developed for the efficient and green synthesis of quinoline-2-thione and …

A new method for the synthesis of pyridine‐and quinoline‐N‐oxides containing a ureido or
carbamoyl fragment in position 2 has been developed. This method concluded in the …