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5. PPh3 Catalyzed Post‐Transformation Ugi‐4CR Intramolecular Cyclization Reaction: One‐Pot Synthesis of Functionalized Spiropyrrolidinochromanones.

6. An insight into tetrahydro-β-carboline–tetrazole hybrids: synthesis and bioevaluation as potent antileishmanial agents† †Electronic supplementary information (ESI) available: 1H and 13C NMR data are available. See DOI: 10.1039/c7md00125h

7. Discovery of a tetrazolyl β-carboline within vitroandin vivoosteoprotective activity under estrogen-deficient conditions

13. Synthesis of diverse 2, 5 Dihydropyrroles via K2CO3 mediated intramolecular carbocyclization of Ugi-MCR precursors.

17. Novel β-carboline–quinazolinone hybrid as an inhibitor of Leishmania donovani trypanothione reductase: Synthesis, molecular docking and bioevaluation

30. Discovery of a New Class of Natural Product-Inspired Quinazolinone Hybrid as Potent Antileishmanial agents

34. Dual targeting of MDM2 with a novel small-molecule inhibitor overcomes TRAIL resistance in cancer.

35. Synthesis of pyrido[1,2-a]imidazo-chalcone via 3-component Groebke-Blackburn-Bienayme reaction and their bioevaluation as potent Antituberculosis Agents.

44. Synthesis of hybrid 4-anilinoquinoline triazines as potent antimalarial agents, their in silico modeling and bioevaluation as Plasmodium falciparumtransketolase and β-hematin inhibitors

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