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Dive into the research topics where Sarita Khandelwal is active.

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Featured researches published by Sarita Khandelwal.


RSC Advances | 2014

Deep eutectic solvent promoted efficient and environmentally benign four-component domino protocol for synthesis of spirooxindoles

Anshu Rajawat; Sarita Khandelwal; M. Kumar

An efficient and environmentally benign one-pot four-component domino protocol has been presented for the synthesis of structurally diverse spirooxindoles spiroannulated with pyrazolopyrimidophthalazines, indenopyrazolophthalazines, chromenopyrazolophthalazines and indazolophthalazines involving the reaction of phthalic anhydride, hydrazine hydrate, isatins and cyclic diketones/diamides in a deep eutectic solvent (choline chloride:urea: 1:2). The present protocol offers some advantages such as operational simplicity with easy workup, shorter reaction times, good to excellent yields with superior atom economy and environmentally benign reaction conditions.


RSC Advances | 2015

An efficient one pot three-component nanocatalyzed synthesis of spiroheterocycles using TiO2 nanoparticles as a heterogeneous catalyst

Yogesh Kumar Tailor; Sarita Khandelwal; Yogita Kumari; Kamlendra Awasthi; M. Kumar

An efficient and environmentally benign isocyanide based domino protocol has been presented for the synthesis of structurally diverse spiroheterocycles, spiroannulated with imidazothiazole and imidazothiadiazole, involving the three component reaction of 2-aminobenzothiazole/2-amino-1,3,4-thiadiazole, cyclohexyl/tert-butyl isocyanides and isatines/cyclic carbonyl compounds catalyzed by recyclable and reusable nanocrystalline TiO2.


Combinatorial Chemistry & High Throughput Screening | 2014

A simple, efficient and environmentally benign synthetic protocol for the synthesis of spirooxindoles using choline chloride-oxalic acid eutectic mixture as catalyst/solvent system.

Sarita Khandelwal; Anshu Rajawat; Yogesh Kumar Tailor; M. Kumar

An efficient and environmentally benign domino protocol has been presented for the synthesis of structurally diverse spirooxindoles spiroannulated with pyranopyridopyrimidines, indenopyridopyrimidines, and chromenopyridopyrimidines involving three-component reaction of aminouracils, isatins and cyclic carbonyl compounds in deep eutectic solvent (choline chloride-oxalic acid: 1:1) which acts as efficient catalyst and environmentally benign reaction medium. The present protocol offers several advantages such as operational simplicity with easy workup, shorter reaction times excellent yields with superior atom economy and environmentally benign reaction conditions with the use of cost-effective, recyclable, non-toxic and bio-degradable DES as catalyst/solvent.


Research on Chemical Intermediates | 2015

Synthesis and evaluation of antioxidant and radical scavenging activities of quinolinobenzothiazinones

M. Kumar; Kshitija Sharma; Anshu Rajawat; Sarita Khandelwal; R.M. Samarth

A new series of structurally diverse quinolinobenzothiazinones has been synthesized with the annulation of heterocyclic structural pharmacophores. The structures of the synthesized compounds were assigned on the basis of their analytical and spectral data. The synthesized quinolinobenzothiazinones were evaluated for their antioxidant (LPO and GSH) and radical scavenging activities (DPPH and ABTS assays).


Green Chemistry Letters and Reviews | 2014

Efficient and environmentally benign synthetic protocol for the synthesis of structurally diverse annulated pyridopyrimidines

Anshu Rajawat; Sarita Khandelwal; M. Kumar

Structurally diverse annulated pyridopyrimidines have been synthesized by an efficient and environmentally benign synthetic protocol involving catalyzed four-component reaction of 2-aminobenzothiazoles with thiophene-2-carbaldehyde and carbonyl compounds in ethanol. Mild reaction conditions, operational simplicity, and structural diversity with excellent yields are some special attractions of the present protocol.


RSC Advances | 2018

An efficient and environmentally sustainable domino protocol for the synthesis of structurally diverse spiroannulated pyrimidophenazines using erbium doped TiO2 nanoparticles as a recyclable and reusable heterogeneous acid catalyst

Kanchan Verma; Yogesh Kumar Tailor; Sarita Khandelwal; Monu Agarwal; Esha Rushell; Yogita Kumari; Kamlendra Awasthi; M. Kumar

An efficient and environmentally sustainable domino protocol has been presented for the synthesis of structurally diverse spiroannulated pyrimidophenazines involving a four component reaction of 2-hydroxynaphthalene-1,4-dione, benzene-1,2-diamine, cyclic ketones and amino derivatives in the presence of erbium doped TiO2 nanoparticles as a recyclable and reusable heterogeneous acid catalyst. The present synthetic protocol features mild reaction conditions with operational simplicity, excellent yield with high purity, short reaction time and high atom economy with the use of a recoverable and reusable environmentally sustainable heterogeneous catalyst.


Journal of Molecular Liquids | 2016

Deep eutectic solvents (DESs) as eco-friendly and sustainable solvent/catalyst systems in organic transformations

Sarita Khandelwal; Yogesh Kumar Tailor; M. Kumar


ChemInform | 2016

L-Proline Catalyzed Multicomponent Reactions

Sarita Khandelwal; Yogesh Kumar Tailor; M. Kumar


Journal of Heterocyclic Chemistry | 2016

Natural Product-Mimetic Scaffolds with Privileged Heterocyclic Systems: Design, Synthesis, and Evaluation of Antioxidant Activity of Quinazoquinobenzothiazinones

Kshitija Sharma; Sarita Khandelwal; R. M. Samarth; M. Kumar


ChemistrySelect | 2017

Diversity-Oriented Synthesis of Spirooxindoles Using Surface-Modified TiO2 Nanoparticles as Heterogeneous Acid Catalyst

Yogesh Kumar Tailor; Sarita Khandelwal; Kanchan Verma; Ram Gopal; M. Kumar

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M. Kumar

Dublin City University

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Ram Gopal

University of Rajasthan

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Esha Rushell

University of Rajasthan

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Anand Kumar Arya

National Council of Educational Research and Training

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Monu Agarwal

University of Rajasthan

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