Year wise Publications
Year wise Publications
Embedded Files
2012
1. Singh S., Srivastava A., Samanta S.* (2012), Rapid access of 2,3,4-trisubstituted-2,3,4,9-tetrahydrothiopyrano[2,3-b]indole derivatives via one-pot three component reaction using organocatalysis, Tetrahedron Lett., 53, 6087-6090 (DOI: 10.1016/j.tetlet.2012.08.125).
2013
2. Srivastava A., Singh S., Samanta S.* (2013), (±)-CSA catalyzed Friedel- Crafts alkylation of indoles with 3-ethoxycarbonyl-3-hydoxyisoindolin-1- one: An easy access of 3-ethoxy carbonyl-3-indolylisoindolin-1-ones bearing a quaternary α-amino acid moiety, Tetrahedron Lett., 54, 1444- 1448 (DOI: 10.1016/j.tetlet.2013.01.010).
3. Jaiswal P. K., Biswas S., Singh S., Samanta S.* (2013), Organocatalytic highly efficient approach to the direct synthesis of substituted carbazoles in water, Org. Biomol. Chem., 11, 8410-8418 (DOI: 10.1039/C3OB42034E).
4. Jaiswal P. K., Biswas S., Singh S., Pathak B., Mobin S. M., Samanta S.* (2013), Stereoselective synthesis of highly functionalized tetrahydro- carbazoles through a domino Michael-Henry reaction: An easy access to four contiguous chiral centers, RSC Adv., 3, 10644-10649 (DOI: 10.1039/C3RA41409D).
5. Biswas S., Jaiswal P. K., Singh S., Mobin S. M., Samanta S.* (2013), L- Proline catalyzed stereoselective synthesis of (E)-methyl-α-indol-2-yl-β- aryl/alkyl acrylates: Easy access to substituted carbazoles, γ-carbolines and prenostodione, Org. Biomol. Chem., 11, 7084-7087 (DOI: 10.1039/C3OB41573B).
2015
6. Singh S., Srivastava A., Mobin S. M., Samanta S.* (2015), A remarkable solvent effect on the reaction of 4-hydroxycoumarin with (E)-3-aryl-2- nitroprop-2-enol: Facile synthesis of highly substituted furo/pyrano[3,2-c]chromenes, RSC Adv., 5, 5010-5014 (DOI: 10.1039/c4ra10610e).
7. Singh S., Samanta S.* (2015), Efficient one-pot access to 2,9- dihydro thiopyrano[2,3-b]indole scaffolds showing large Stokes Shifts, Chin. J. Chem., 2015, 33, 1244-1250 (DOI: 10.1002/cjoc.201500572).
8. Srivastava A., Biswas S., Singh S., Mobin S. M., Samanta S.* (2015), Organocatalyzed Michael addition on arylmethylidenemalonates involving 4-(2-nitrophenyl) acetoacetate: Diversity oriented access to 8,9- dihydropyrido[1,2-a]indol-6(7H)-one and salicylate scaffolds, RSC Adv., 5, 26891-26896 (DOI: 10.1039/c5ra01430a).
2020
9. Chhakra S., Malhotra G. S., Singh S.,Chauhan S. S. (2020), Synthesis of novel substituted pyrazoles and isoxazoles containing 1,4-benzodi-oxane sulfonyl moiety, Rasayan J. of Chemistry, 13, 3 1959-1963. (DOI: 10.31788/ RJC.2020.1335863).
2021
10. Singh S., Chauhan S. S., Sharma N. K., Dutt S. and Ameta K. L.* (2021), Diverse Routes for the synthesis of Indole-fused Complex Architecture from Simple Molecules, Mini-reviews in Organic Chemistry, 18, 2, 237-258 (DOI:10.2174/1570193X17999200521101).
11. Singh N., Naaz F., Verma R., Singh S., Singh R. K. (2021), Photophysical studies on drug conjugates of stavudine/zidovudine and 1,8-naphthalimide in different solvent systems, Asian Journal of Chemistry, 33, 11, 2729-2736 (DOI: 10.14233/ajchem.2021.23348)
11. Singh N., Naaz F., Verma R., Singh S., Singh R. K. (2021), Photophysical studies on drug conjugates of stavudine/zidovudine and 1,8-naphthalimide in different solvent systems, Asian Journal of Chemistry, 33, 11, 2729-2736 (DOI: 10.14233/ajchem.2021.23348)
2022
12. Devi A. P., Dhingra N., Bhardwaj U., Chundawat R. S., Joshi C. K., Singh S. and Ameta K. L. (2022), 2-(phenyl)-4H-chromen-4-ones: Green Synthesis, characterization, in vitro antifungal evaluation and molecular docking approach toward Aspergillus fumigatus, Current Research in Green and Sustainable Chemistry, Vol. 5, 100234 (DOI: 10.1016/j.crgsc.2021.100234)
12. Devi A. P., Dhingra N., Bhardwaj U., Chundawat R. S., Joshi C. K., Singh S. and Ameta K. L. (2022), 2-(phenyl)-4H-chromen-4-ones: Green Synthesis, characterization, in vitro antifungal evaluation and molecular docking approach toward Aspergillus fumigatus, Current Research in Green and Sustainable Chemistry, Vol. 5, 100234 (DOI: 10.1016/j.crgsc.2021.100234)
13. Singh N., Rajotiya K., Lamba N., Singh H. L., Ameta K. L., Singh S. (2022), Versatile approach for the synthesis of furocoumarin derivatives, Current Organic Chemistry, 26, 3, 324-341 (DOI: 10.2174/1385272826666220126155703)
13. Singh N., Rajotiya K., Lamba N., Singh H. L., Ameta K. L., Singh S. (2022), Versatile approach for the synthesis of furocoumarin derivatives, Current Organic Chemistry, 26, 3, 324-341 (DOI: 10.2174/1385272826666220126155703)
14. Sharma A., Singh S., Singh H. L. (2022), Lead(II) Schiff Base Complexes: Design, Synthesis, Theoretical, Antibacterial and Docking Studies, Asian Journal of Chemistry, Vol. 34, No. 4, 945-952 (DOI: https://doi.org/10.14233/ajchem.2022. 23634 )
14. Sharma A., Singh S., Singh H. L. (2022), Lead(II) Schiff Base Complexes: Design, Synthesis, Theoretical, Antibacterial and Docking Studies, Asian Journal of Chemistry, Vol. 34, No. 4, 945-952 (DOI: https://doi.org/10.14233/ajchem.2022. 23634 )
15. Sharma R., Dutt S., Singh S. (2022), Swollen liquid crystals as soft and structure-directing templates to synthesize polyindole nanostructures having distinctive electrochemical properties, Asian Journal of Chemistry, 34, 6, 1413-1418 (doi:10.14233/ajchem.2022.23647 )
15. Sharma R., Dutt S., Singh S. (2022), Swollen liquid crystals as soft and structure-directing templates to synthesize polyindole nanostructures having distinctive electrochemical properties, Asian Journal of Chemistry, 34, 6, 1413-1418 (doi:10.14233/ajchem.2022.23647 )
16. Sharma S., Singh S. (2022), Synthetic routes to quinoline-based derivatives having potential Anti-bacterial and Anti-fungal properties, Curr. Org. Chem., Vol-26, Issue-15, 1453-1469, DOI: 10.2174/1385272827666221021140934)
16. Sharma S., Singh S. (2022), Synthetic routes to quinoline-based derivatives having potential Anti-bacterial and Anti-fungal properties, Curr. Org. Chem., Vol-26, Issue-15, 1453-1469, DOI: 10.2174/1385272827666221021140934)
2023
17. Sharma S. and Singh S. (2023), Molecular Docking Study for binding affinity of 2H-thiopyrano[2,3-b]quinoline derivatives against CB1a, Interdisciplinary Perspectives on Infectious Diseases, Vol 2023, 1-10, https://doi.org/10.1155/2023/1618082
17. Sharma S. and Singh S. (2023), Molecular Docking Study for binding affinity of 2H-thiopyrano[2,3-b]quinoline derivatives against CB1a, Interdisciplinary Perspectives on Infectious Diseases, Vol 2023, 1-10, https://doi.org/10.1155/2023/1618082
18. Sharma S., Singh K., and Singh S. (2023), Synthetic strategies for Quinoline-based derivatives as potential bioactive heterocycles, Curr. Org. Synth., 20 (6), 606-629, DOI: 10.2174/1570179420666221004143910)Â
18. Sharma S., Singh K., and Singh S. (2023), Synthetic strategies for Quinoline-based derivatives as potential bioactive heterocycles, Curr. Org. Synth., 20 (6), 606-629, DOI: 10.2174/1570179420666221004143910)Â
19. Dutt S., Kumar A. and Singh S. (2023), Synthesis of Metal Organic Frameworks (MOFs) and their derived materials for energy storage applications, Clean Technologies (MDPI) 5 (1), 140-166, https://doi.org/10.3390/cleantechnol5010009
19. Dutt S., Kumar A. and Singh S. (2023), Synthesis of Metal Organic Frameworks (MOFs) and their derived materials for energy storage applications, Clean Technologies (MDPI) 5 (1), 140-166, https://doi.org/10.3390/cleantechnol5010009
20. Kathal R., Sharma S., Singh K., and Singh S. (2023), Simplified procedure for application of DBE, The rule of 13 & Nitrogen rule in structure elucidation of organic compounds, Lett. in Org. Chem, Vol-20, Issue-3, 276-286. DOI: 10.2174/1570178619666220902120311
20. Kathal R., Sharma S., Singh K., and Singh S. (2023), Simplified procedure for application of DBE, The rule of 13 & Nitrogen rule in structure elucidation of organic compounds, Lett. in Org. Chem, Vol-20, Issue-3, 276-286. DOI: 10.2174/1570178619666220902120311
21. Sharma S., Yadav D. and Singh S. (2023), Quinoline Derivatives and Analogues: Synthesis and Anti-Oncogenic Activity, Medicinal Chemistry, 19 (9), 848-858 (DOI: 10.2174/1573406419666230411110025)
21. Sharma S., Yadav D. and Singh S. (2023), Quinoline Derivatives and Analogues: Synthesis and Anti-Oncogenic Activity, Medicinal Chemistry, 19 (9), 848-858 (DOI: 10.2174/1573406419666230411110025)
22. Sharma S., Monga Y., Gupta A. and Singh S. (2023), 2-Oxindole and related Heterocycles: Synthetic Methodologies for the Natural Products and related Derivatives, RSC Advances, 13, 14249-14267, DOI: 10.1039/d3ra02217jÂ
22. Sharma S., Monga Y., Gupta A. and Singh S. (2023), 2-Oxindole and related Heterocycles: Synthetic Methodologies for the Natural Products and related Derivatives, RSC Advances, 13, 14249-14267, DOI: 10.1039/d3ra02217jÂ
23. Sharma S., Monga Y., Gupta A. and Singh S. (2023), A review on indole[2,3-a]quinolizidine: the synthetic approaches to the development of bioactive indole[2,3-a]quinolizidine scaffolds, Heterocycles, Vol. 106, No. 11, (DOI : 10.3987/REV-23-1008)
23. Sharma S., Monga Y., Gupta A. and Singh S. (2023), A review on indole[2,3-a]quinolizidine: the synthetic approaches to the development of bioactive indole[2,3-a]quinolizidine scaffolds, Heterocycles, Vol. 106, No. 11, (DOI : 10.3987/REV-23-1008)
24. Sharma S. and Singh S. (2023), The Biological and Pharmacological Potentials of Indole Heterocyclics, Lett. in Organic Chemistry, Vol. 20, Issue-8, 711-729 (DOI: 10.2174/1570178620666230215121808)
24. Sharma S. and Singh S. (2023), The Biological and Pharmacological Potentials of Indole Heterocyclics, Lett. in Organic Chemistry, Vol. 20, Issue-8, 711-729 (DOI: 10.2174/1570178620666230215121808)
25. Sharma S. and Singh S. (2023), Bioactive Indole Heterocycles and their Synthetic Routes: A Comprehensive Review, Current Trends in Biotechnology and Pharmacy, Vol. 17 (3A), 1141-1158, 10.5530/ctbp.2023.3s.52.
25. Sharma S. and Singh S. (2023), Bioactive Indole Heterocycles and their Synthetic Routes: A Comprehensive Review, Current Trends in Biotechnology and Pharmacy, Vol. 17 (3A), 1141-1158, 10.5530/ctbp.2023.3s.52.
26. Sharma S., Monga Y., Gupta A. and Singh S. Â (2023), In silico screening and molecular docking study of quinoline based compounds with Human kallikrein 7 in complex with 1,4-diazepane-7-one-1-acetamide derivative receptor target for potential antibacterials, J. of Mol. Chem., Vol. 3 (1), 585.
26. Sharma S., Monga Y., Gupta A. and Singh S. Â (2023), In silico screening and molecular docking study of quinoline based compounds with Human kallikrein 7 in complex with 1,4-diazepane-7-one-1-acetamide derivative receptor target for potential antibacterials, J. of Mol. Chem., Vol. 3 (1), 585.
27. Kandpal B. M., Tyagi R., Tehlan S., Singh S., Gupta R., Monga Y., and Gupta A. Â (2023), 4-Amino-3-hydrazino-5-mercapto-1,2,4,-triazole (PURPALD) in organic chemicals analysis: Distinguishing aldehydes and ketones, Jour. of Int. Sc. and Tech., Vol. 12 (1), 709.
27. Kandpal B. M., Tyagi R., Tehlan S., Singh S., Gupta R., Monga Y., and Gupta A. Â (2023), 4-Amino-3-hydrazino-5-mercapto-1,2,4,-triazole (PURPALD) in organic chemicals analysis: Distinguishing aldehydes and ketones, Jour. of Int. Sc. and Tech., Vol. 12 (1), 709.
28. Sharma S., Mishra A. K. and Singh S. (2023), Molecular docking study of 2,3,4- trisubstituted-2,3,4,9-tetrahydrothiopyrano[2,3-b]indole derivatives with TRPV channels: Possible new analgesics, Eng. and Tech. Jour. for Res. and Inn. (ETJRI), Vol 5, Issue 01.
28. Sharma S., Mishra A. K. and Singh S. (2023), Molecular docking study of 2,3,4- trisubstituted-2,3,4,9-tetrahydrothiopyrano[2,3-b]indole derivatives with TRPV channels: Possible new analgesics, Eng. and Tech. Jour. for Res. and Inn. (ETJRI), Vol 5, Issue 01.
2024
29. Sharma S., Mishra P. K. and Singh S. (2024), Comprehensive outline, bioactivities, and useful synthetic routes for the different classes of flavonoids, Mini-Reviews in Org. Chem., DOI: 10.2174/1570193X21666230901110030
29. Sharma S., Mishra P. K. and Singh S. (2024), Comprehensive outline, bioactivities, and useful synthetic routes for the different classes of flavonoids, Mini-Reviews in Org. Chem., DOI: 10.2174/1570193X21666230901110030
30. Sharma S., Choubey R., Gupta M., and Singh S. (2024), Heterocyclic-Based Analogues against Sarcine-Ricin Loop RNA from Escherichia coli: In Silico Molecular Docking Study and Machine Learning Classifiers, Med. Chem., Vol. 20 (4), 452-465, DOI: Â 10.2174/0115734064266329231228050535
30. Sharma S., Choubey R., Gupta M., and Singh S. (2024), Heterocyclic-Based Analogues against Sarcine-Ricin Loop RNA from Escherichia coli: In Silico Molecular Docking Study and Machine Learning Classifiers, Med. Chem., Vol. 20 (4), 452-465, DOI: Â 10.2174/0115734064266329231228050535
31. Singh S., Sharma S., Das S. and Das A. K. (2024), Spider Silk: Biosynthesis, Properties & Bioengineering, Curr. Nanomater., Vol. 9, Issue 2, 83-91 (DOI: 10.2174/2405461508666230502115035)
31. Singh S., Sharma S., Das S. and Das A. K. (2024), Spider Silk: Biosynthesis, Properties & Bioengineering, Curr. Nanomater., Vol. 9, Issue 2, 83-91 (DOI: 10.2174/2405461508666230502115035)
32. Sharma S., Singh D., Singh K. and Singh S. (2024), Recent Developments in the Medicinal Chemistry of Functionalized Carbon Nanotubes (Submitted)
32. Sharma S., Singh D., Singh K. and Singh S. (2024), Recent Developments in the Medicinal Chemistry of Functionalized Carbon Nanotubes (Submitted)
33. Monga Y., Sharma S., Gupta A. and Singh S. (2024), Biochar, Clay, Zeolites, and Microorganism-Based Methods for Remediation of Heavy Metals, Current Green Chemistry, Vol-11, Issue-1, 2-11 DOI: 10.2174/2213346110666230915140448
33. Monga Y., Sharma S., Gupta A. and Singh S. (2024), Biochar, Clay, Zeolites, and Microorganism-Based Methods for Remediation of Heavy Metals, Current Green Chemistry, Vol-11, Issue-1, 2-11 DOI: 10.2174/2213346110666230915140448
34. Singh R., Sharma S., Singh S. and Singh K. (2024), Thiazole and Thiazolidinone Derivatives as Anti-inflammatory Agents, Book Chapter, Pp: 94-116 (23), DOI: 10.2174/9789815223460124010008
34. Singh R., Sharma S., Singh S. and Singh K. (2024), Thiazole and Thiazolidinone Derivatives as Anti-inflammatory Agents, Book Chapter, Pp: 94-116 (23), DOI: 10.2174/9789815223460124010008
Book Detail: Heterocyclic Anti-Inflammatory Agents: A Guide for Medicinal Chemists
Book Detail: Heterocyclic Anti-Inflammatory Agents: A Guide for Medicinal Chemists
ISBN: 978-981-5223-47-7 (Print)
ISBN: 978-981-5223-46-0 (Online)
35. Sharma S., Singh R., Singh K. and Singh S. (2024), Coumarins and Their Derivatives as Anti-Inflammatory Agents, Book Chapter, Pp: 208-230 (23), DOI: 10.2174/9789815223460124010013
35. Sharma S., Singh R., Singh K. and Singh S. (2024), Coumarins and Their Derivatives as Anti-Inflammatory Agents, Book Chapter, Pp: 208-230 (23), DOI: 10.2174/9789815223460124010013
Book Detail: Heterocyclic Anti-Inflammatory Agents: A Guide for Medicinal Chemists
Book Detail: Heterocyclic Anti-Inflammatory Agents: A Guide for Medicinal Chemists
ISBN: 978-981-5223-47-7 (Print)
ISBN: 978-981-5223-46-0 (Online)
36. Sharma S., Dutt S. and Singh S. (2024), Lithium-ion batteries for sustainable technologies and low-carbon future: A Comprehensive Review, (Submitted)
36. Sharma S., Dutt S. and Singh S. (2024), Lithium-ion batteries for sustainable technologies and low-carbon future: A Comprehensive Review, (Submitted)
37. Singh S., Samanta S. (2024), Catalyst-free reaction of 4-mercaptocoumarin with (E)-3-aryl/hetero-aryl-substituted-2-nitroprop-2-enols/Morita-Baylis-Hillman acetates of nitro-olefins: Facile synthesis of 4-sulfanylcoumarins. (Under Preparation)
37. Singh S., Samanta S. (2024), Catalyst-free reaction of 4-mercaptocoumarin with (E)-3-aryl/hetero-aryl-substituted-2-nitroprop-2-enols/Morita-Baylis-Hillman acetates of nitro-olefins: Facile synthesis of 4-sulfanylcoumarins. (Under Preparation)
38. Sharma S. and Singh S. (2024), Antibacterial/Antifungal activity and Synthetic Aspects of Indole Heterocycles/Related Frameworks: A Comprehensive Review
38. Sharma S. and Singh S. (2024), Antibacterial/Antifungal activity and Synthetic Aspects of Indole Heterocycles/Related Frameworks: A Comprehensive Review
39. Shrivastava P., Yadav D., Singh S. K., Kim S. H., Singh S., Katiyar S. and Song M. (2024), Investigating Bacopa Monnieri L. Therapeutic Potential for the treatment of Neurological Diseases, Current Pharmaceutical Design, 30, 1016-1030.
39. Shrivastava P., Yadav D., Singh S. K., Kim S. H., Singh S., Katiyar S. and Song M. (2024), Investigating Bacopa Monnieri L. Therapeutic Potential for the treatment of Neurological Diseases, Current Pharmaceutical Design, 30, 1016-1030.
2025
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