This review article describes methods for the preparation of pyrrolo [1, 2-a] quinoxalines,
covering literature sources from the last 10 years. The attention was largely paid to new …

As a privileged class of heterocyclic compounds N-heteroarenes have found enormous
applications in many areas including medicinal/pharmaceutical chemistry and drug …

Following our search for antimalarial compounds, novel series of ferrocenyl-substituted
pyrrolo [1, 2-a] quinoxalines 1-2 were synthesized from ferrocene-carboxaldehyde and …

Herein we describe the synthesis and properties of substituted phenylaminopyrrolo [1, 2-a]
quinoxaline-carboxylic acid derivatives as a novel class of potent inhibitors of the human …

Novel series of bis-and tris-pyrrolo [1, 2-a] quinoxaline derivatives 1 were synthesized and
tested for in vitro activity upon the intraerythrocytic stage of W2 and 3D7 Plasmodium …

Herein, we describe novel iron-catalyzed transfer hydrogenation between alcohols and 1-(2-
nitrophenyl) pyrroles for the synthesis of pyrrolo [1, 2-α] quinoxalines. The tricarbonyl (η4 …

An efficient NCS-promoted thiocyanation of pyrrolo [1, 2-a] quinoxalines with NH4SCN or
KSCN is described. A series of diverse 1-thiocyanatopyrrolo [1, 2-a] quinoxalines were …

The first enantioselective synthesis of 5, 6-dihydroindolo [1, 2-a] quinoxalines is achieved by
using a newly developed H8-BINOL-type imidodiphosphoric acid catalyst with low catalyst …

Herein, we describe the direct synthesis of pyrrolo [1, 2-α] quinoxaline via oxidative coupling
between methyl arene and 1-(2-aminophenyl) pyrroles. Oxidation of the benzylic carbon of …

Together with estrogen receptors ERα and ERβ, the G protein‐coupled estrogen receptor
(GPER) mediates important pathophysiological signaling pathways induced by estrogens …