Vadde Ravinder

Design and synthesis of spiro[indole-thiazolidine]spiro[indole-pyrans] as antimicrobial agents

Indoles as therapeutics of interest in medicinal chemistry: Bird's eye view

Iron Catalysis in Organic Synthesis

Saccharomyces cerevisiae catalyzed one pot synthesis of isoindolo[2,1-a]quinazoline performed under ultrasonication

Copper-Catalyzed Sequential Ullmann N-Arylation and Aerobic Oxidative C–H Amination: A Convenient Route to Indolo[1,2-c]quinazoline Derivatives

Au^I‐Catalyzed Direct Hydroamination/Hydroarylation and Double Hydroamination of Terminal Alkynes

Cesium Carbonate‐Promoted Hydroamidation of Alkynes: Enamides, Indoles and the Effect of Iron(III) Chloride

Multicomponent reactions: advanced tools for sustainable organic synthesis

Aerobic Copper-Catalyzed Organic Reactions

Organocatalytic Reactions Enabled by N-Heterocyclic Carbenes

Gold-Catalyzed Carbon−Heteroatom Bond-Forming Reactions

Organocatalysis emerging as a technology

N-Heterocyclic carbene catalyzed intramolecular crossed aldehyde–ketone benzoin condensation in the chalcone of o-phthalaldehyde: a facile synthesis of naphthalenones

Asymmetric organocatalysis: an enabling technology for medicinal chemistry

Mono and bis-6-arylbenzimidazo[1,2-c]quinazolines: A new class of antimicrobial agents

Physicochemical and biological characterization of novel macrocycles derived from o-phthalaldehyde

Antimicrobial study of newly synthesized 6-substituted indolo[1,2-c]quinazolines

6‐Substituted Indolo[1,2‐c]quinazolines as New Antimicrobial Agents