49. Electrochemical Synthesis: An Alliance of Electrochemistry and Organic Synthesis for Value-Added Moieties
S. S. Badsara*, K. Ucheniya, A. Chouhan, A., Chem. Rec. 2025, 00, e202500092
https://onlinelibrary.wiley.com/doi/10.1002/tcr.202500092
Embedded Files
48. Electrochemical Synthesis of Ketones via Metal-Free Decarboxylative Coupling of Vinyl Azides and NHPI Esters
B. Jat, H. Verma, S. S. Badsara*, S. Sharma*, Synlett, 2025, 36, 2275-2278
https://www.thieme-connect.com/products/ejournals/abstract/10.1055/a-2608-2142
47. Recent Advances in Electrochemical Utilization of NHPI Esters.
B. Jat, D. K. Yadav, S. S. Badsara*, S. Sharma* , Org. Biomol. Chem., 2025, 23, 4846-4854.
https://doi.org/10.1039/D5OB00467E
46. Palladium-catalyzed reductive cross-coupling reaction of carboxylic acids with thiols: An alternative strategy to access thioesters
Y-T. Chang, R. Bai, Y.-T. Hsia, I. Karmakar, S. S. Badsara*, S. Lee*,CF. Lee* , Org. Biomol. Chem., 2025, Advance Article
45. Zinc-catalyzed N-aroylation of sulfoximines with carboxylic acids
Z-W. Chen, R. Bai, P. Annamalai, S. S. Badsara, C-F. Lee, Chem. Asian J. 2024, e202400780
44. Rapid access to triarylmethanes (TRAMs) enabled by direct electrolysis of indolizines with carbonyls
P. K. Jat, S. S. Badsara, J. Org. Chem., 2024, 89, 12263.
https://doi.org/10.1021/acs.joc.4c01198
43. Electrochemical selective divergent C-H chalcogenocyanation of N-heterocyclic scaffolds
K. Ucheniya,† P. K. Jat,† A. Chouhan, S. S. Badsara, Org. Biomol. Chem., 2024, 22, 3220.
†These authors contributed equally and both are joint first authors.
https://doi.org/10.1039/D4OB00448E
C-F. Lee, R. Bai, K-C. Liu, Z-W. Chen, A. Gurjar, S. S. Badsara, Arkivoc 2023 (ii) 202312055
A. Chouhan, K. Ucheniya, L. Yadav, P. K. Jat, A. Gurjar, S. S. Badsara, Org. Biomol. Chem., 2023, 21, 7643.
W-C. Chen, R. Bai, W-L. Cheng, C-Y. Peng, D. M. Reddy, S. S. Badsara, C-F. Lee, Org. Biomol. Chem., 2023, 21, 3002.
K. Ucheniya, A. Chouhan, L. Yadav, P. K. Jat, S. S. Badsara, J. Org. Chem., 2023, 88, 6096.
P. K. Jat, L. Yadav, A. Chouhan, K. Ucheniya, S. S. Badsara, Chem. Commun., 2023, 59, 5415.
36. Electrochemical Bisarylation of Carbonyls: A Direct Synthetic Strategy for Bis(indolyl)methane
P. K. Jat, K. K. D abaria, R. Bai, L. Yadav, S. S. Badsara, J. Org. Chem., 2022, 87, 12975.
35. Electrochemical Cascade Thia-Michael and Thioacetalization of Cyclic Enones
L. Yadav, K. K. Dabaria, P. K. Jat, A. Gurjar, S. S. Badsara, Synthesis, 2022, 54, 5479.
K. K. Dabaria, R. Bai, S. S. Badsara, ChemistrySelect, 2022, 7, e202202992.
33. Cesium Carbonate-Catalyzed Synthesis of Phosphorothioates via S-Phosphination of Thioketones
Z-W. Chen, P. Annamalai, R. Bai, Y. Hu, S. S. Badsara, K-W. Huang, C-Fa Lee, Chem. Commun., 2022, 58, 11001.
K. K. Dabaria, R. Bai, P. K. Jat, S. S. Badsara, New J. Chem., 2022, 46, 12905.
31. Blue LED-Mediated Syntheses of Arylazo Phosphine Oxides and Phosphonates via N-P Bond Formation
B-R. Shen, P. Annamalai, R. Bai, S. S. Badsara, C-F. Lee, Org. Lett., 2022, 24, 5988.
R. Bai, K. K. Dabaria, S. S. Badsara, Synthesis, 2022, 54, 2487.
29. The journey of C-S bond formations from metal to electro catalysis
Z-W. Chen, R. Bai, P. Annamalai, S. S. Badsara, Chin-Fa Lee, New J. Chem., 2022, 46, 15 (Perspective).
28. Carbon-Sulfur Bond Constructions: From Transition-Metal Catalysis to Sustainable Catalysis
P. Annamalai, K-C. Liu, S. S. Badsara, C.-F. Lee, Chem. Rec., 2021, 21, 3674 (Personal Account).
B. K. Malviya, K. Singh, P. Jaiswal, M. Karnatak, V. P. Verma, S. S. Badsara, S. Sharma, New. J. Chem., 2021, 45, 6367.
B. K. Malviya, P. K. Jaiswal, V. P. Verma, S. S. Badsara, S. Sharma, Org. Lett., 2020, 22, 2323.
25. Highly Atom-Economic, Catalyst-free, and Solvent-free Phosphorylation of Chalcogenides
R. Choudhary, P. Singh, R. Bai, M. C. Sharma, S. S. Badsara, Org. Biomol. Chem., 2019, 17, 9757.
S. S. Badsara, P. Singh, R. Choudhary, R. Bai, M. C. Sharma, New. J. Chem., 2019, 43, 11045.
K. Singh, B. K. Malviya, V. P. Verma, S. S. Badsara, V. K. Bhardwaj, S. Sharma, Tetrahedron, 2019, 75, 2506.
22. Engineered C-S bond construction
C-F. Lee, R. S. Basha, S. S. Badsara, Top. Curr. Chem., 2018, 376, 25. (Springer International Publishing AG, part of Springer Nature 2018).
R. Bai, R. Choudhary, P. Singh R. Thakuria, M. C. Sharma, S. S. Badsara, ChemistrySelect, 2018, 3, 3221.
20. Room temperature, open flask C-P bond formation on water under catalyst-free conditions
R. Choudhary, R. Bai, P. Singh, M. C. Sharma, S. S. Badsara, SynOpen, 2018, 2, 213.
19. Regio- and stereoselective syntheses of allylic thioethers under metal free conditions
P. Singh, R. Bai, R. Choudhary, M. C. Sharma, S. S. Badsara, RSC Adv., 2017, 7, 30594.
R. Choudhary, R. Bai, P. Singh, M. C. Sharma, S. S. Badsara, Tetrahedron, 2017, 73, 4323.
17. Peracetic Acid Mediated sp2 C-H Selenation of Arenes
P-A. Hsieh, S. S. Badsara, C.-H Tsai, D. M. Reddy, C-F. Lee, Synlett, 2016, 27, 1557.
16. CuCl/TBHP catalyzed synthesis of amides from aldehydes and amines in water
S-Y. Lu, S. S. Badsara, Y-C Wu, D. M. Reddy, C.-F Lee, Tetrahedron Lett, 2016, 57, 633.
15. K2S2O8/I2 Promoted Syntheses of α-Thio-β-dicarbonyl Compounds via Oxidative C-S Coupling Reactions Under Transition Metal-Free and Solvent-Free Conditions
Y.-W. Liu, S. S. Badsara, Y.-C. Liu, C.-F. Lee, RSC Adv., 2015, 5, 44299.
14. Formal synthesis of a disaccharide repeating unit (IdoA–GlcN) of heparin and heparan sulfate
R. C. Sawant, Y-J Liao, Y-J. Lin, S. S. Badsara, S-Y Luo, RSC Adv., 2015, 5, 19027.
13. Microwave-assisted copper-catalyzed cross-coupling reaction of thiols with aryl iodides in water
Y-A. Chen, S. S. Badsara, W-T. Tsai, C-F. Lee, Synthesis 2015; 47, 181.
S. S. Badsara, C. Chan, C-F. Lee, Asian J. Org. Chem. 2014, 3, 1197.
11. Synthesis of ganglioside Hp-s1
W-S. Chen, R. C. Sawant, S-A. Yang, Y-J. Liao, J-W. Liao, S. S. Badsara, S-Y. Luo, RSC Adv., 2014, 4, 47752.
R. C. Sawant, Y-H. Lih, S-A. Yang, C-H. Yeh, H-J. Tai, C-L. Huang, H-S. Lin, S. S. Badsara, S-Y.Luo, RSC Adv., 2014, 4, 26524.
9. Copper-catalyzed cross-coupling reaction of thiols with aryl iodides under ligand-free conditions
Y-T. Huang, W-T. Tsai, S. S.Badsara, C-C. Chan,C-F. Lee, J. Chin. Chem. Soc. 2014, 61, 967.
S. S. Badsara, Y-C. Liu, P-A. Hsieh, J-W. Zeng, S-Y. Lu, Y-W. Liu, C-F. Lee, Chem. Commun., 2014, 50, 11374.
J-C. Liou, S. S. Badsara, Y-T. Huang, C-F Lee, RSC Adv., 2014, 4, 41237.
J-W. Zeng, Y-C. Liu, P-A. Hsieh, Y-T. Huang, C-L. Yi, S. S. Badsara, C-F. Lee, Green Chem., 2014, 16, 2644.
5. Transition-Metal-Catalyzed C-S Bond Coupling Reaction
C-F. Lee, Y-C. Liu, S. S. Badsara, Chem. Asian J. 2014, 9, 706 (Focus Review).
D. Basavaiah, G. Veeraraghavaiah, S. S. Badsara, Org. Biomol. Chem., 2014, 12, 1551.
D. Basavaiah, S. S. Badsara, G. Veeraraghavaiah, Tetrahedron, 2013, 69, 7995.
D. Basavaiah, S. S. Badsara, B. C. Sahu, Chem Eur. J. 2013, 19, 2961.
1. Recent contributions from the Baylis-Hillman reaction to organic chemistry
D. Basavaiah, B. S. Reddy, S. S. Badsara, Chem. Rev., 2010, 110, 5447.
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