A practical and convenient approach for the secondary C (sp3)–H arylation of
diarylmethanes with various fluoroarenes is described. The reaction proceeds smoothly in …

Over the past few decades, furopyridines have emerged as key structural subunits prevalent
in a number of natural products and structural analogues associated with interesting …

A small library of twelve, structurally diverse, fluoroaryl benzimidazoles was prepared using
a simple synthetic strategy employing SN Ar reactions. This allowed rapid assembly of …

Annelation reaction between pentafluoropyridine and diaminodihydro substituted pyridine
derivatives gave dipyrido [1, 2‐b: 3′, 4′‐e][1, 2, 4] triazine systems as major products …

A series of new halogenated aryl sulfonamides, as bio-active candidates, was synthesized
from the reaction of the corresponding aryl sulfonamides with pentafluoro-and …

A transition metal-free strategy is reported for the site-selective O-arylation of cyclic 1, 3-
dicarbonyls with polyfluoroarenes. This method offers a straightforward and alternative …

In this paper, site reactivity of amidoximes with pentafluoropyridine under basic conditions in
dry CH 3 CN was investigated. The aromatic nucleophilic substitution of pentafluoropyridine …

Chemo selectivity of some N-aryl formamides with pentafluoropyridine under basic
conditions in dry THF was investigated. The aromatic nucleophilic substitution of …

Site reactivity of some enol–imines derived from N-aryl formamides with pentachloropyridine
under basic conditions in dry CH3CN was investigated. The aromatic nucleophilic …

A new series of 4‐hetroaryl substituted quinazolines were designed and synthesized by the
reaction of pentafluoro (chloro) pyridine and 2‐substituted quinazolinone. The aromatic …