Subbu perumal, Ph.D
Affiliations: | chemistry | Madurai Kamaraj University |
Google:
"Subbu perumal"Mean distance: (not calculated yet)
Parents
Sign in to add mentorN. Arumugam | grad student | Madurai Kamaraj University | |
C. Srinivasan | grad student | Madurai Kamaraj University | |
Alan Roy Katritzky | post-doc | UF Gainesville |
Children
Sign in to add traineeCollaborators
Sign in to add collaboratorAndrea Mazzanti | collaborator | UniversitA de bologna | |
Jose carlos menendez | collaborator | Universidad Complutense de Madrid (Spain) |
BETA: Related publications
See more...
Publications
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
Kumar SV, Muthusubramanian S, Perumal S. (2019) Recent Progress in the Synthesis of Pyrazolopyridines and Their Derivatives Organic Preparations and Procedures International. 51: 1-89 |
Vachan BS, Karuppasamy M, Vinoth P, et al. (2019) Proline and its Derivatives as Organocatalysts for Multi‐ Component Reactions in Aqueous Media: Synergic Pathways to the Green Synthesis of Heterocycles Advanced Synthesis & Catalysis. 362: 87-110 |
Kumar SV, Rani GU, Divyalakshmi M, et al. (2018) Synthesis of benzosuberone-tethered spirooxindoles: 1-3-dipolar cycloaddition of azomethine ylides and arylidene benzosuberones. Molecular Diversity |
Uma Maheswari S, Vivek Kumar S, Muthusubramanian S, et al. (2018) A facile solvent-free three-component domino synthesis of novel 2,4-diaryl-5,6-dihydrobenzo[j][1,7]phenanthrolines. Molecular Diversity |
Bharkavi C, Vivek Kumar S, Ashraf Ali M, et al. (2017) One-pot microwave assisted stereoselective synthesis of novel dihydro-2'H-spiro[indene-2,1'-pyrrolo-[3,4-c]pyrrole]-tetraones and evaluation of their antimycobacterial activity and inhibition of AChE. Bioorganic & Medicinal Chemistry Letters |
Bharkavi C, Vivek Kumar S, Ashraf Ali M, et al. (2016) A facile stereoselective synthesis of dispiro-indeno pyrrolidine/pyrrolothiazole-thiochroman hybrids and evaluation of their antimycobacterial, anticancer and AchE inhibitory activities. Bioorganic & Medicinal Chemistry |
Uma Rani G, Vivek Kumar S, Bharkavi C, et al. (2016) One-pot access to a library of dispiro oxindole-pyrrolidine/pyrrolothiazole-thiochromane hybrids via three-component 1,3-dipolar cycloaddition reactions. Acs Combinatorial Science |
Kumar SV, Muthusaravanan S, Muthusubramanian S, et al. (2016) An efficient one pot three-component domino reaction for the synthesis of 1,3,4-trisubstituted pyrroles Chemistryselect. 1: 675-679 |
Kumar SV, Muthusaravanan S, Muthusubramanian S, et al. (2016) ChemInform Abstract: An Efficient One Pot Three-Component Domino Reaction for the Synthesis of 1,3,4-Trisubstituted Pyrroles. Cheminform. 47 |
Viswanathan V, Bharkavi S, Perumal S, et al. (2015) Crystal structures of two 2,9-di-thia-13-aza-dispiro-[4.1.4(7).3(5)]tetra-decan-6-ones. Acta Crystallographica. Section E, Crystallographic Communications. 71: 1516-20 |