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Kapil Arya

Researcher at Indian Oil Corporation

Publications -  12
Citations -  230

Kapil Arya is an academic researcher from Indian Oil Corporation. The author has contributed to research in topics: Catalysis & Antimycobacterial. The author has an hindex of 5, co-authored 12 publications receiving 215 citations. Previous affiliations of Kapil Arya include University of Delhi.

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Microwave prompted multigram synthesis, structural determination, and photo-antiproliferative activity of fluorinated 4-hydroxyquinolinones.

TL;DR: A simple facile one-step microwave enhanced multigram synthesis of such fluorinated quinolones in reasonable purity has been developed in excellent yield in 3-5 min, whereas conventional synthesis required the harsh conditions, long reaction period with use of environmentally unacceptable regents giving the required product in lower yield.
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Synthesis and cytotoxic activity of trisubstituted-1,3,5-triazines.

TL;DR: A simple and environmentally friendly procedure has been developed for the synthesis of 1,3,5-triazine derivatives under microwave irradiation in the presence of a HY zeolite, which provides a simple and green synthetic methodology under environmentally friendly conditions.
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The expedient synthesis of 1,5-benzothiazepines as a family of cytotoxic drugs.

TL;DR: The expedient synthesis of 1,5-benzothiazepines using LaY zeolite under stirring condition is reported and synthesized compound screened for cytotoxic activity provides a simple and green synthetic methodology under environmentally friendly conditions.
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Proline confined FAU zeolite: heterogeneous hybrid catalyst for the synthesis of spiroheterocycles via a Mannich type reaction

TL;DR: In this paper, a novel L-proline confined FAU zeolite catalyst system has been developed by confinement of Lproline in faujasite zeolites and its catalytic activity has been tested in the aqueous mediated synthesis of novel 1′,3′-di-(4-methylphenyl)-2′, 3′,4′,6′-tetrahydro-1′H-spiro[indene-2,5′-pyrimidin]-1(3H)-one (4d) for the first
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Synthesis of biologically important novel fluorinated spiro heterocycles under microwaves catalyzed by montmorillonite KSF

TL;DR: In this paper, arylidienes of fluorinated spiro thiazolidines containing α,β-unsaturated function have been used as component of Micheal addition with equimolar amount of 2-aminopyridine (6a) to give novel fluorinated SPIRIN [indole-3,2′-pyrido[1,2-a]thiazolo[5,4-e]pyrimidines] (7) in a single step under microwaves in presence of montmorillonite KSF as solid support