Triazoles are important five-membered heterocyclic scaffold due to their extensive biological
activities. This framework can be readily obtained in good to excellent yields on the …

Abstract The copper (I)‐catalyzed 1, 2, 3‐triazole‐forming reaction between azides and
terminal alkynes has become the gold standard of 'click chemistry'due to its reliability …

A series of novel 1, 2, 3-triazole-dithiocarbamate hybrids were designed, synthesized and
evaluated for anticancer activity against four selected human tumor cell lines (MGC-803 …

Cancer is a class of formidable disease with high degree of mortality. Despite much
progress in chemotherapy, the problem of drug resistance has led to the search for newer …

1, 4-Disubstituted-1 H-1, 2, 3-triazoles 1 can easily be distinguished from the isomeric 1, 5-
disubstituted-1 H-1, 2, 3-triazoles 2 by simple one-dimensional 13C NMR spectroscopy …

The triazole ring system has emerged as an exciting prospect in the optimization studies of
promising lead molecules in the quest for new drugs for clinical usage. Several marketed …

We, herein, reported the CuI catalyzed synthesis of some novel fused benzothiazole-1, 2, 3-
triazole hybrids (5a-5o) in one-pot. The in vitro anticancer activity of these compounds …

We describe here the synthesis and activity of a new series of oxime reactivators of
cholinesterases (ChEs) that contain tertiary amine or imidazole protonatable functional …

Abstract A series of novel 1, 2, 3-triazole–pyrimidine–urea hybrids were designed,
synthesized and evaluated for anticancer activity against four selected cancer cell lines …

A series of novel 1, 2, 3-triazole–dithiocarbamate–urea hybrids were designed, synthesized
and their antiproliferative activities against four selected human cancer cell lines were …