The burgeoning interest in synthesis and biological applications of 1, 6-naphthyridines
reflects the importance of 1, 6-naphthyridines in the synthetic as well as medicinal chemistry …

A metal/additive‐free, TBHP‐promoted synthesis of 12H‐Chromeno [2, 3‐b] quinolin‐12‐
ones from 2‐phenoloxyquinolinyl‐3‐carboxaldehydes has been described via cross …

A novel procedure for the synthesis of various derivatives of 6H-chromeno [4, 3-b] quinolines
from intramolecular Heck reaction of 2-chloro-3-(phenoxymethyl) quinolines is described in …

A metal-free, TBHP-promoted economical route is developed via the sp2 C–H bond
functionalization strategy for the synthesis of indenoquinolinones, 4-azafluorenones and …

Ag (I)-Catalyzed one-pot synthesis of 4-fluorobenzo [b][1, 6] naphthyridines is described
from o-alkynylquinolinyl aldehydes through imines in good to excellent yields. Selectfluor is …

Abstract Substituted chromeno [4, 3‐b] quinolines and [1, 6] naphthyridines were achieved
by tandem intramolecular aza‐Diels–Alder reaction using a strategy of combination of …

A straightforward and atom-economical one-pot protocol catalyzed by gold (I) and zinc (II) for
the synthesis of amine-substituted diaryl [c, h][1, 6] naphthyridines from two different …

Pd mediated one pot sequential Sonogashira coupling followed by annulation using o-
alkynyl aldehyde is reported. Contrary to the established modes of ring closures, an unusual …

An efficient tandem approach for the chemoselective synthesis of functionalized azido-
pyranoquinolines and azido-iodo-pyranoquinolines via electrophilic cyclization of o …

A convenient method for the facile synthesis of 1-trifluoromethyl-3-alkylidene-1, 3-
dihydrofuro [3, 4-b] quinolines was developed from the TBAB-catalyzed nucleophilic …