A new methodology is developed for the efficient synthesis of 1, 3-diketone-linked N-
substituted pyrroles, pyrrolo [1, 2-a] pyrazines, pyrrolo [1, 4] diazepines, and pyrrolo [1, 4] …

A straightforward protocol toward pharmacologically relevant (het) areno [x, yb] pyrrolo [1, 2-
d][1, 4] diazepines in good to high yields has been described. The designed approach …

A simple one-pot method for the synthesis of isomeric pyrrolo [1, 2-x][1, 4] diazepinones in
reasonable yields was developed. The method is based on the condensation of readily …

A new method for the synthesis of pyrrolo [1, 2-d][1, 4] benzodiazepines is described. The
method is based on the acid-catalyzed recyclization of N-[2-(5-alkyl-2-furyl) phenyl]-2 …

An efficient synthesis of alkyl 7-hydroxy-1-oxo-1, 2, 3, 4-tetrahydropyrrolo [1, 2-a] pyrazine-8-
carboxylate derivatives by reaction between diamines, dialkyl acetylenedicarboxylates, and …

The copper chloride catalyzed and iodine-mediated oxidative annulation of N-furfuryl-β-
enaminones, generated in situ from reactions of furfurylamines with ynones, provides a …

Abstract An efficient synthesis of 1, 3, 4‐trisubstituted pyrroles via three‐component domino
reactions of (E)‐3‐(dimethylamino)‐1‐arylprop‐2‐en‐1‐ones, anilines and β‐nitrostyrenes …

One of the most important properties of furan compounds widely used in synthetic practice is
their ability to undergo ring opening to form 1, 4-diketones [1]. Hence the protolytic opening …

Aim and Objective: A new approach to synthesis of isoindoles condensed with other
heterocycles and revelation of their spatial structure for biochemistry purposes was the main …

Abstract Treatment of β-dicarbonyls with the Furakawa-variant of the Simmons-Smith
reagent results in homologation and production of an intermediate zinc enolate. Treatment …