Prakash Prajapat
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Prakash Prajapat has a total of 23 co-authors. Here are the top co-authors by number of shared publications:
- Divyani Gandhi
Synthetic Organic Chemistry Laboratory, Department of Chemistry, MLSU, Udaipur, Rajasthan, India
2 shared publications Priyanka Kalal
Department of Chemistry, University College of Science, Mohanlal Sukhadia University, Udaipur, India
2 shared publicationsShikha Agarwal
Department of Chemistry, Synthetic Organic Chemistry Laboratory, Mohanlal Sukhadia University, Udaipur 313001, India
2 shared publications- Shikha Agarwal
Synthetic Organic Chemistry Laboratory, Department of Chemistry, Mohanlal Sukhadia University, Udaipur-313001, Rajasthan, India
2 shared publications - Ajit Joshi
Synth. Org. Chem. Lab., Dep. Chem., M. L. Sukhadia Univ., Udaipur 313 001, India
1 shared publication Ayushi Sethiya
Synthetic Organic Chemistry Laboratory, Department of Chemistry, MLSU, Udaipur, Rajasthan, India
1 shared publication
Latest Publications
- 26 October 2020
- Published by Bentham Science Publishers Ltd. in Current Nanomaterials
- Vol. 5 (2) , 111-157
Graphene Oxide Membrane: Recent Advancement in Waste Water Treatment and its Applications
World water resources are barely alive due to various factors such as rise in population, adverse changes in the environment and the effects of pollutants, which increase the demand for fresh-water. Numerous techniques have been developed to solve the problem of water inadequacy, but most of them are adverse with respect to the environment and economy. Graphene-oxide (GO) nanopore materials may be an effective solution for water-purification due to its properties of easy fabrication and modification. This next-generation membrane has high waterflux, selectivity, and permeability to selected molecules. In this discussion, we have covered the latest technologies and potential applications of GO for waterpurification, which shall help researchers to get quick ideas for future research to design and fabricate multi-layered GO membranes. This article gives a snapshot of current status and proposed strategies of graphene-membranes for water treatment with earlier information to wastewater management and stimulated progress in this area from 2017 to date. The future challenges and opportunities in this field have also been highlighted.
- 26 October 2020
- Published by Bentham Science Publishers Ltd. in Current Nanomaterials
- Vol. 5 (2) , 111-157
Graphene Oxide Membrane: Recent Advancement in Waste Water Treatment and its Applications
World water resources are barely alive due to various factors such as rise in population, adverse changes in the environment and the effects of pollutants, which increase the demand for fresh-water. Numerous techniques have been developed to solve the problem of water inadequacy, but most of them are adverse with respect to the environment and economy. Graphene-oxide (GO) nanopore materials may be an effective solution for water-purification due to its properties of easy fabrication and modification. This next-generation membrane has high waterflux, selectivity, and permeability to selected molecules. In this discussion, we have covered the latest technologies and potential applications of GO for waterpurification, which shall help researchers to get quick ideas for future research to design and fabricate multi-layered GO membranes. This article gives a snapshot of current status and proposed strategies of graphene-membranes for water treatment with earlier information to wastewater management and stimulated progress in this area from 2017 to date. The future challenges and opportunities in this field have also been highlighted.
- 1 January 2020
- Published by Bentham Science Publishers Ltd. in Letters in Organic Chemistry
- Vol. 17 (2) , 141-148
Design, Synthesis and Antimicrobial Study of Novel 1-(1,3-benzothiazol-2-yl)-3-chloro-4H-spiro[azetidine-2,3′-indole]-2′,4(1′H)-diones Through Ketene-imine Cycloaddition Reaction
The present study deals with the synthesis of novel 1-(1,3-benzothiazol-2-yl)-3-chloro-4H-spiro[azetidine-2,3'-indole]-2',4-(1'H)-dione derivatives from the reaction of 3-(1,3-benzothiazol-2-ylimino)-1,3-dihydro-2H-indol-2-one derivatives with chloroacetyl chloride in the presence of triethylamine (TEA). The mechanism involved simple acid or base catalysed reaction through the formation of Schiff base followed by cyclisation via ketene-imine cycloaddition reaction. All synthesized cornpounds were characterized by FT-IR, H-1-NMR, C-13-NMR, and elemental analysis. The antimicrobial activities of the synthesized derivatives 5a-5g were examined via Micro Broth Dilution method against bacterial strains Bacillius subtilis, Staphylcoccus aureus, E. coli, P. aeruginosa, and fungal strain Candida albicans for determining MIC values. Ampicillin, chloramphenicol, and griseofulvin were used as standard drugs. The MIC values for antimicrobial activity of synthesized compounds were examined using Micro Broth Dilution method. Compounds 5a, 5b, and 5c were found effective against E. coli (MTCC 442) and P.aeruginosa (MTCC 441) and all compounds showed moderate to excellent activity against Streptococcus aureus (MTCC 96) and Bacillius subtilis (MTCC 441). Regarding the antifungal screening, compounds 5a, 5b, and 5c exhibited excellent activity against Candida albicans MTCC 227. 1-(1,3-benzothiazol-2-yl)-3-chloro-4H-spiro[azetidine-2,3'-indole]-2',4(1'H)-dione derivatives may be used as potential lead molecules as effective antimicrobial agents.
- 1 January 2020
- Published by Bentham Science Publishers Ltd. in Letters in Organic Chemistry
- Vol. 17 (2) , 141-148
Design, Synthesis and Antimicrobial Study of Novel 1-(1,3-benzothiazol-2-yl)-3-chloro-4H-spiro[azetidine-2,3′-indole]-2′,4(1′H)-diones Through Ketene-imine Cycloaddition Reaction
The present study deals with the synthesis of novel 1-(1,3-benzothiazol-2-yl)-3-chloro-4H-spiro[azetidine-2,3'-indole]-2',4-(1'H)-dione derivatives from the reaction of 3-(1,3-benzothiazol-2-ylimino)-1,3-dihydro-2H-indol-2-one derivatives with chloroacetyl chloride in the presence of triethylamine (TEA). The mechanism involved simple acid or base catalysed reaction through the formation of Schiff base followed by cyclisation via ketene-imine cycloaddition reaction. All synthesized cornpounds were characterized by FT-IR, H-1-NMR, C-13-NMR, and elemental analysis. The antimicrobial activities of the synthesized derivatives 5a-5g were examined via Micro Broth Dilution method against bacterial strains Bacillius subtilis, Staphylcoccus aureus, E. coli, P. aeruginosa, and fungal strain Candida albicans for determining MIC values. Ampicillin, chloramphenicol, and griseofulvin were used as standard drugs. The MIC values for antimicrobial activity of synthesized compounds were examined using Micro Broth Dilution method. Compounds 5a, 5b, and 5c were found effective against E. coli (MTCC 442) and P.aeruginosa (MTCC 441) and all compounds showed moderate to excellent activity against Streptococcus aureus (MTCC 96) and Bacillius subtilis (MTCC 441). Regarding the antifungal screening, compounds 5a, 5b, and 5c exhibited excellent activity against Candida albicans MTCC 227. 1-(1,3-benzothiazol-2-yl)-3-chloro-4H-spiro[azetidine-2,3'-indole]-2',4(1'H)-dione derivatives may be used as potential lead molecules as effective antimicrobial agents.
- 1 November 2019
- Published by Prints Publications Pvt Ltd in THE JOURNAL OF PLANT SCIENCE RESEARCH
- Vol. 35 (2) , 233-241
Alteration in Physiological and Biochemical Activities of Azadirachta indica in Presence of Air Pollutants
Shop for The Journal of Plant Science Research online at best price on India's Largest Bookstore, Prints Publications. ✯Best Prices ✯Easy Returns. Visit Us or Call@ +91-11-45355555
- 1 November 2019
- Published by Prints Publications Pvt Ltd in THE JOURNAL OF PLANT SCIENCE RESEARCH
- Vol. 35 (2) , 233-241
Alteration in Physiological and Biochemical Activities of Azadirachta indica in Presence of Air Pollutants
Shop for The Journal of Plant Science Research online at best price on India's Largest Bookstore, Prints Publications. ✯Best Prices ✯Easy Returns. Visit Us or Call@ +91-11-45355555
- 2 July 2018
- Published by Bentham Science Publishers Ltd. in Current Drug Discovery Technologies
- Vol. 15 (3) , 178-195
Thiazole Containing Heterocycles with CNS Activity
Thiazoles are promising scaffolds in the area of medicinal and pharmaceutical chemistry and have accounted to show different pharmacophoric properties. For the last years, thiazole derivatives have focused too much attention to develop different new CNS active agents. It has been broadly used to generate diverse therapeutic agents against various CNS targets. Histamine H3 receptors are seriously involved in the pathophysiology of numerous disorders of the central nervous system. The literature survey has been done using different database from peerreviewed journals. The quality of repossessed papers was evaluated using standard tools. The details of important papers were described to focus on the potency of thiazole containing heterocycles with CNS activity. Eighty nine papers were included in the review indicating thiazole containing heterocycles with CNS activity. (1) to (30) papers included different thiazole derivatives impregnated withCNS activity. Different CNS agents have been shown in references (37) to (56). The remaining papers have been searched for anticonvulsant agents (57) to (78) and other miscellaneous activities from (79) to (89). A detailed investigation has been carried out on thiazoles and its derivatives to judge its efficacy to overcome several CNS disorders. This article covers the recent updates of thiazole and its derivative with CNS activity already present in literature and will definitely provide a better platform for the production and development of potent thiazole based CNS vigorous drugs in near future.
- 2 July 2018
- Published by Bentham Science Publishers Ltd. in Current Drug Discovery Technologies
- Vol. 15 (3) , 178-195
Thiazole Containing Heterocycles with CNS Activity
Thiazoles are promising scaffolds in the area of medicinal and pharmaceutical chemistry and have accounted to show different pharmacophoric properties. For the last years, thiazole derivatives have focused too much attention to develop different new CNS active agents. It has been broadly used to generate diverse therapeutic agents against various CNS targets. Histamine H3 receptors are seriously involved in the pathophysiology of numerous disorders of the central nervous system. The literature survey has been done using different database from peerreviewed journals. The quality of repossessed papers was evaluated using standard tools. The details of important papers were described to focus on the potency of thiazole containing heterocycles with CNS activity. Eighty nine papers were included in the review indicating thiazole containing heterocycles with CNS activity. (1) to (30) papers included different thiazole derivatives impregnated withCNS activity. Different CNS agents have been shown in references (37) to (56). The remaining papers have been searched for anticonvulsant agents (57) to (78) and other miscellaneous activities from (79) to (89). A detailed investigation has been carried out on thiazoles and its derivatives to judge its efficacy to overcome several CNS disorders. This article covers the recent updates of thiazole and its derivative with CNS activity already present in literature and will definitely provide a better platform for the production and development of potent thiazole based CNS vigorous drugs in near future.
- 25 May 2018
- Published by Bentham Science Publishers Ltd. in Combinatorial Chemistry & High Throughput Screening
- Vol. 21 (4) , 236-253
Diversity Oriented Synthesis of 4H-Pyrimido[2,1-b]benzothiazole Derivatives via Biginellis Reaction: A Review
Background: Heterocycles have extended into widespread use for generating large collection of molecules in multi-component reactions. The development of new strategies for fused pyrimidobenzothiazole system has remained a highly attractive but challenging proposition for scientists working all around. Objective: The main objective of this work is to explore the utility of different catalysts as an ecofriendly reaction medium for green Biginellis reaction. Method: A detailed study of Biginellis reactions using various catalysts was done using different research tools. The methods involved reaction of equimolar mixture of benzothiazole, 1,3-diketone and aldehyde as reactants by conventional and greener pathways via Knoevenagal condensation. Results: The present review has several significant advantages for the scientists regarding green synthesis viz. green conditions, short reaction times, high yields, clean reaction conditions, easy isolation of products, simple work-up procedure and mild reaction conditions. Conclusion: Our report gives an overview of the combinatorial libraries for fused benzothiazole entities using metal catalyst, acid catalyst, ionic liquids, phase transfer catalyst, nano catalyst, etc.
- 25 May 2018
- Published by Bentham Science Publishers Ltd. in Combinatorial Chemistry & High Throughput Screening
- Vol. 21 (4) , 236-253
Diversity Oriented Synthesis of 4H-Pyrimido[2,1-b]benzothiazole Derivatives via Biginellis Reaction: A Review
Background: Heterocycles have extended into widespread use for generating large collection of molecules in multi-component reactions. The development of new strategies for fused pyrimidobenzothiazole system has remained a highly attractive but challenging proposition for scientists working all around. Objective: The main objective of this work is to explore the utility of different catalysts as an ecofriendly reaction medium for green Biginellis reaction. Method: A detailed study of Biginellis reactions using various catalysts was done using different research tools. The methods involved reaction of equimolar mixture of benzothiazole, 1,3-diketone and aldehyde as reactants by conventional and greener pathways via Knoevenagal condensation. Results: The present review has several significant advantages for the scientists regarding green synthesis viz. green conditions, short reaction times, high yields, clean reaction conditions, easy isolation of products, simple work-up procedure and mild reaction conditions. Conclusion: Our report gives an overview of the combinatorial libraries for fused benzothiazole entities using metal catalyst, acid catalyst, ionic liquids, phase transfer catalyst, nano catalyst, etc.
- Open Access
- 20 March 2018
- Published by Juniper Publishers in Organic & Medicinal Chemistry International Journal
- Vol. 5 (5)
New Benzothiazole-Thiazolidinone hybrids containing Phthalimidoxy and Ethoxyphthalimide: Design, Synthesis and Pharmacological Assay
Organic and Medicinal chemistry international Journal is an open access journal that is committed to publish the papers on various topics of chemistry, especially synthetic organic chemistry, and pharmacology and various other biological specialties
- 20 March 2018
- Published by Juniper Publishers in Organic & Medicinal Chemistry International Journal
- Vol. 5 (5)
Open AccessNew Benzothiazole-Thiazolidinone hybrids containing Phthalimidoxy and Ethoxyphthalimide: Design, Synthesis and Pharmacological Assay
Organic and Medicinal chemistry international Journal is an open access journal that is committed to publish the papers on various topics of chemistry, especially synthetic organic chemistry, and pharmacology and various other biological specialties
- Open Access
- 24 January 2018
- Published by Lupine Publishers LLC in Archives of Organic and Inorganic Chemical Sciences
- Vol. 1 (1) , 001-002
Role of Combinatorial, Medicinal & Biological Chemistry in Drug Discovery Development: An Introduction
Combinatorial chemistry, a new approach for greatly reducing the time for the discovery of newer organic motifs, has been developed over the last few years
- 24 January 2018
- Published by Lupine Publishers LLC in Archives of Organic and Inorganic Chemical Sciences
- Vol. 1 (1) , 001-002
Open AccessRole of Combinatorial, Medicinal & Biological Chemistry in Drug Discovery Development: An Introduction
Combinatorial chemistry, a new approach for greatly reducing the time for the discovery of newer organic motifs, has been developed over the last few years
- Open Access
- 4 January 2018
- Published by Crimson Publishers in Modern Approaches in Drug Designing
- Vol. 1 (4)
Importance of Benzothiazole Motif in Modern Drug Discovery: Introduction
- 4 January 2018
- Published by Crimson Publishers in Modern Approaches in Drug Designing
- Vol. 1 (4)
Open AccessImportance of Benzothiazole Motif in Modern Drug Discovery: Introduction
- 6 December 2016
- Published by Wiley in ChemInform
- Vol. 47 (52)
ChemInform Abstract: An Expedient Synthesis and anti‐Microbial Evaluation of Ethoxyphthalimido Derivatives of Pyrimido[4,5‐e]pyrimidine Analogues from 1‐(1H‐Benzimidazol‐2‐yl)guanidine.
Some of the new compounds, e.g. (Xd), exhibit high antibacterial and antifungal activity similar to the reference drugs.
- 6 December 2016
- Published by Wiley in ChemInform
- Vol. 47 (52)
ChemInform Abstract: An Expedient Synthesis and anti‐Microbial Evaluation of Ethoxyphthalimido Derivatives of Pyrimido[4,5‐e]pyrimidine Analogues from 1‐(1H‐Benzimidazol‐2‐yl)guanidine.
Some of the new compounds, e.g. (Xd), exhibit high antibacterial and antifungal activity similar to the reference drugs.
- 31 May 2016
- Published by Wiley in Journal of Heterocyclic Chemistry
- Vol. 54 (2) , 993-998
One-pot Synthesis of Bis[1-N,7-N-diethoxyphthalimido-4,4′-{3,5-dimethyl-4-(4-N,N-dimethyl Aminophenyl)-4,7-dihydro-1H-dipyrazolo[3,4-b;4′,3′-e]Pyridin-8-yl}-phenyl] Compounds and Their Antiviral Evaluation Against Cytomegalovirus (CMV) and Varicella-zoste
- 31 May 2016
- Published by Wiley in Journal of Heterocyclic Chemistry
- Vol. 54 (2) , 993-998
One-pot Synthesis of Bis[1-N,7-N-diethoxyphthalimido-4,4′-{3,5-dimethyl-4-(4-N,N-dimethyl Aminophenyl)-4,7-dihydro-1H-dipyrazolo[3,4-b;4′,3′-e]Pyridin-8-yl}-phenyl] Compounds and Their Antiviral Evaluation Against Cytomegalovirus (CMV) and Varicella-zoste