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A Facile Synthesis of 5-Acylbarbituric Acids under Microwave Irradiation.

Synthesis of 5-Acyl-6-[2-hydroxy-3-(amino)propylamino] -1,3-dialkyl-1H-pyrimidine-2,4-diones (VI).

A Simple Synthesis of 5-Spirobarbituric Acids and Transformations of Spirocyclopropanobarbiturates to 5-Substituted Barbiturates.

A Practical Approach for Spiro- and 5-Monoalkylated Barbituric Acids.

ChemInform Abstract: 1-Toluene-sulfonyl-3- [(3′-hydroxy-5′-substituted)-γ-butyrolactone]-indoles: Synthesis, COX-2 Inhibition and Anticancer Activities.

ChemInform Abstract: Design, Synthesis and Anticancer Activities of Hybrids of Indole and Barbituric Acids — Identification of Highly Promising Leads.

A practical approach for spiro- and 5-monoalkylated barbituric acids

Synthesis of pyrazole-based hybrid molecules: Search for potent multidrug resistance modulators

1-Toluene-sulfonyl-3-[(3′-hydroxy-5′-substituted)-γ-butyrolactone]-indoles: Synthesis, COX-2 inhibition and anti-cancer activities

2,3,5-Substituted tetrahydrofurans as cancer chemopreventives. Part 1: Synthesis and anti-cancer activities of 5-hydroxymethyl-2,3-diaryl-tetrahydro-furan-3-ols

Search for MDR modulators: Design, syntheses and evaluations of N-substituted acridones for interactions with p-glycoprotein and Mg2+

Targeting efflux pumps—In vitro investigations with acridone derivatives and identification of a lead molecule for MDR modulation

Design, synthesis and anticancer activities of hybrids of indole and barbituric acids—Identification of highly promising leads

2,3,5-Substituted tetrahydrofurans: COX-2 inhibitory activities of 5-hydroxymethyl-/carboxyl-2,3-diaryl-tetrahydro-furan-3-ols

Synthesis and evaluation of indole, pyrazole, chromone and pyrimidine based conjugates for tumor growth inhibitory activities – Development of highly efficacious cytotoxic agents