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Narsidas J. Parmar

Observed names: N. J. Parmar, N.J. Parmar, Narsidas Jeramdas Parmar, Narsidas Parmar, PARMAR, NARSIDAS, Parmar, N.J., Parmar, Narsidas, Parmar, Narsidas J.
ORCID: 0000-0003-4580-7249
Observed ORCID: 0000-0003-4580-7249
OpenAlex ID: A5113212980
An efficient one-pot synthesis, structure, antimicrobial and antioxidant investigations of some novel quinolyldibenzo[b,e][1,4]diazepinones
2012 · Narsidas J. Parmar, Hitesh A. Barad, et al. · Bioorganic & Medicinal Chemistry Letters · 44
Synthesis, antimicrobial and antioxidant activities of some 5-pyrazolone based Schiff bases
2011 · Narsidas Parmar, Shashikant Teraiya, et al. · Journal of Saudi Chemical Society · 43
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An efficient domino reaction in ionic liquid: Synthesis and biological evaluation of some pyrano- and thiopyrano-fused heterocycles
2013 · Narsidas J. Parmar, Rikin A. Patel, et al. · Bioorganic & Medicinal Chemistry Letters · 39
Efficient synthesis of some new antiproliferative N-fused indoles and isoquinolines via 1,3-dipolar cycloaddition reaction in an ionic liquid
2015 · Tushar R. Sutariya, Balvantsingh M. Labana, et al. · New Journal of Chemistry · 36
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A highly efficient, rapid one-pot synthesis of some new heteroaryl pyrano[2,3-c]pyrazoles in ionic liquid under microwave-irradiation
2013 · Narsidas J. Parmar, Hitesh A. Barad, et al. · RSC Advances · 35
Tetrabutylammonium hydrogen sulfate mediated domino reaction: synthesis of novel benzopyran-annulated pyrano[2,3-c]pyrazoles
2011 · Narsidas J. Parmar, Shashikant B. Teraiya, et al. · Tetrahedron Letters · 32
Access to Some Angular Aminochromeno[2,3‐c]pyrazole Precursors by a Domino Knoevenagel–hetero‐Diels–Alder Reaction
2012 · Narsidas J. Parmar, Bhavesh R. Pansuriya, et al. · European Journal of Organic Chemistry · 28
New pyrazolyl-dibenzo[b,e][1,4]diazepinones: room temperature one-pot synthesis and biological evaluation
2019 · Gaurangkumar C. Brahmbhatt, Tushar R. Sutariya, et al. · Molecular Diversity · 24
Chelation and extraction of copper(II) with 5-pyrazolone-based Schiff bases
2011 · N.J. Parmar, H.A. Barad, et al. · Journal of Coordination Chemistry · 21
A Base-Catalyzed, Domino Aldol/hetero-Diels–Alder Synthesis of Tricyclic Pyrano[3,4-c]chromenes in Glycerol
2016 · Bhagyashri D. Parmar, Tushar R. Sutariya, et al. · The Journal of Organic Chemistry · 20
Catalyst-and solvent-free one-pot synthesis of some novel polyheterocycles from aryldiazenyl salicylaldehyde derivatives
2012 · Narsidas J. Parmar, Rikin A. Patel, et al. · RSC Advances · 20
A glycerol mediated domino reaction: an efficient, green synthesis of polyheterocycles incorporating a new thiochromeno[2,3-b]quinoline unit
2013 · Narsidas J. Parmar, Hitesh A. Barad, et al. · RSC Advances · 19
An improved microwave assisted one-pot synthesis, and biological investigations of some novel aryldiazenyl chromeno fused pyrrolidines
2012 · Narsidas J. Parmar, Bhavesh R. Pansuriya, et al. · Bioorganic & Medicinal Chemistry Letters · 19
An efficient synthesis of some thiopyranopyrazole-heterocycles via domino reaction in a Brønsted acidic ionic liquid
2014 · Narsidas J. Parmar, Bhagyashri D. Parmar, et al. · Tetrahedron Letters · 18
An efficient domino Knoevenagel/hetero-Diels–Alder route to some novel thiochromenoquinoline-fused polyheterocycles
2014 · Narsidas J. Parmar, Balvantsingh M. Labana, et al. · Monatshefte für Chemie - Chemical Monthly · 16
Triethylammonium acetate-mediated domino-Knoevenagel-hetero-Diels–Alder reaction: synthesis of some angular polyheterocycles
2012 · Narsidas J. Parmar, Bhavesh R. Pansuriya, et al. · Monatshefte für Chemie - Chemical Monthly · 16
A convenient 1,3-dipolar cycloaddition–reduction synthetic sequence from 2-allyloxy-5-nitro-salicylaldehyde to aminobenzopyran-annulated heterocycles
2013 · Narsidas J. Parmar, Bhavesh R. Pansuriya, et al. · RSC Advances · 15
Efficient One-Pot Synthesis of Precursors of Some Novel Aminochromene Annulated Heterocycles via Domino Knoevenagel–hetero-Diels–Alder Reaction
2013 · Narsidas J. Parmar, Shashikant B. Teraiya, et al. · Synthetic Communications · 14
A domino synthetic approach for new, angular pyrazol- and isoxazol-heterocycles using [DBU][Ac] as an effective reaction medium
2015 · Tushar R. Sutariya, Balvantsingh M. Labana, et al. · RSC Advances · 13
Solvent-free, one-pot synthesis and biological evaluation of some new dipyrazolo [3,4-b:4′,3′-e]pyranylquinolones and their precursors
2013 · Narsidas J. Parmar, Bhavesh R. Pansuriya, et al. · Medicinal Chemistry Research · 13
Cobalt(II) and nickel(II) chelates of some 5-pyrazolone-based, Schiff-base ligands
2009 · N. J. Parmar, S. B. Teraiya · Journal of Coordination Chemistry · 11
Efficient synthesis and biological evaluation of new benzopyran-annulated pyrano[2,3-c]pyrazole derivatives
2017 · Balvantsingh M. Labana, Gaurangkumar C. Brahmbhatt, et al. · Molecular Diversity · 10
One-pot synthesis, biological evaluation, and docking study of new chromeno-annulated thiopyrano[2,3-c]pyrazoles
2016 · Bhagyashri D. Parmar, Tushar R. Sutariya, et al. · Molecular Diversity · 10
A catalyst- and solvent-free multicomponent synthesis and docking study of some new antiproliferative N 5 -allyl-quinolylpyrido[2,3-b][1,4]benzodiazepinone precursors
2016 · Hitesh A. Barad, Tushar R. Sutariya, et al. · New Journal of Chemistry · 10
Oxovanadium(IV), Cr(III), Fe(III), Fe(II), Ni(II), Cu(II), Zn(II), and UO2(VI) Chelates from Onno Donor Schiff Base Ligand
2005 · R. N. Jadeja, N. J. Parmar · Synthesis and Reactivity in Inorganic Metal-Organic and Nano-Metal Chemistry · 9
Works count: 74
Citation count: 565
H-index: 16
I10-index: 24
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