Anticancer agents are critical for the cancer treatment, but side effects and the drug
resistance associated with the currently used anticancer agents create an urgent need to …

Triazole moiety which is usually constructed by highly versatile, efficacious and selective
copper-catalyzed azide-alkyne cycloaddition not only can act as a linker to connect different …

A general strategy was developed for the synthesis of new fully decorated 1, 2, 3-triazoles
(5a-m & 6a-e) containing coumarine and sulfonyl-benzimidazole from 3-(2-((1-methyl-1H …

An efficient synthesis of a variety of [1, 2, 3] triazolo-[1, 5-a] quinoxalin-4 (5 H)-ones via a [3+
2] cyclization reaction by photoredox catalysis between quinoxalinones and hypervalent …

Herein, a new series of N-substituted 1, 2, 3-triazolylmethyl indole derivatives 4 (a–u) was
synthesized by rationally incorporating a pharmacophoric active heterocyclic ring containing …

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 …

Herein, we synthesized some new fused [1, 2, 3] triazolo-pyrrolo [1, 2-a] pyrido [4, 3-d]
pyrimidines via click chemistry followed by carbon-carbon bond coupling as key approach …

A one‐step procedure for the synthesis of new fused Benzo [d] thiazolo‐1, 2, 3‐triazoles (3 a–
3 h and 4 a–4 h) in good yields using sulfonylazides (2) and iodoalkyne (1) through from the …

A series of homoerythrina alkaloid derivatives containing a 1, 2, 3-triazole moiety as PARP-1
inhibitors were designed and synthesized. And their anti-proliferative activity was further …

In this study, we designed and synthesized several novel fused [1, 2, 3] triazolo [4′, 5′: 3,
4] pyrrolo [2, 1-b] quinazolinone derivatives using a single [3+ 2] reaction cycloaddition …