Quinoline derivatives are very widely known biologically active heterocyclic compounds, as
for example quinine, mefloquine, etc. In recent years, the interests of researchers are …

The unique reactivity of allenes has led to their emergence as valuable coupling partners in
transition-metal-mediated C–H activation reactions. On the other hand, due to its high …

The C (8)-selective nucleophilic cascade cyclization of quinoline N-oxide with easily derived
1, 6-enyne from phenol derivatives is demonstrated. A variety of quinoline N-oxide and …

In this review, we spotlight the methods for the direct synthesis of synthetically and
biologically important 1-sulfonyl-1, 2, 3-triazoles via [3+ 2] cycloaddition between easily …

Solvent-promoted and-controlled regioselective bond alkylation reactions of para-quinone
methides (p-QMs) with N–H free-indoline and 1, 2, 3, 4-tetrahydroquinoline (THQ) under …

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 …

Herein, we report a novel rhodium/selenium dual catalytic process for the synthesis of 2-
aminopyrroles from N-sulfonyl-1, 2, 3-triazoles. The proposed cooperative catalytic …

In order to obtain new supramolecular ligands that build up around a zinc‐porphyrin
scaffold, we envisioned to access sulfonyl triazole intermediates by well‐known copper …

The development and implementation of innovative synthetic methods that incorporate
sustainable reagents and solvents are crucial aspects in both academic and industrial …

The cycloaddition of N-sulfonyl and N-sulfamoyl azides with terminal alkynes generally
produces amide derivatives via ketenimine intermediates. We herein delineate a Cu (I) …