Publications

Synthesis of new kojic acid based unnatural ?-amino acid derivatives.

Balakrishna C, Payili N, Yennam S, Uma Devi P, Behera M

Bioorg Med Chem Lett. 2015 Nov 1;25(21):4753-6. doi: 10.1016/j.bmcl.2015.07.099

Pd catalyzed C–N Bond Forming Reactions of 6-Bromo-2-cyclopropyl-3-(pyridyl-3-ylmethyl)-4-quinazolin-(3H)-one at Room Temperature

Narender Pottabathini, Ramesh Garlapati, Venkateshwarlu Gurram, Suresh Poudapally, Pavan Kumar Machirajub, Somesh Sharma

Current Organocatalysis, 2213-3372

Facile and short synthesis of (+) 1-hydroxy indolizidine and (+) coniceine from picolinic acid ethyl ester via cross claisen condensation

S. Veeraswamy, R. Venkat Ragavan, Y. Narasimha Reddy, Satyanarayana Yennam, A. Jayashree

Asian Journal of Chemistry; 27(5) 1667-1670, 2015

Synthesis, in vitro anticancer and antimycobacterial evaluation of new 5-(2,5-dimethoxyphenyl)-1,3,4-thiadiazole-2-amino derivatives

Naveen Polkam, Parsharamulu Rayam, Jaya Shree Anireddy, Satyanarayana Yennam, Hasitha Shilpa Anantaraju, Sriram Dharmarajan, Yogeeswari Perumal, Sudha Sravanti Kotapalli, Ramesh Ummanni, Sridhar Balasubramanian

Bioorganic & Medicinal Chemistry Letters; 25 (2015) 1398–1402

Mild and General Access to Diverse 1H-Benzotriazoles via Diboron-Mediated N–OH Deoxygenation, and Pd-Catalyzed C–C and C–N Bond Formation

Venkateshwarlu Gurram, Hari K Akula, Ramesh Garlapati, Narender Pottabathini, Mahesh K. Lakshman

Adv. Synth. Catal. 2015, 357, 451-462

Design, synthesis, and biological evaluation of quinazoline derivatives as a-glucosidase inhibitors

Venkateshwarlu Gurram, Ramesh Garlapati, Chiranjeevi Thulluri, Nagaraju Madala, Kumara Swamy Kasani, Pavan Kumar Machiraju, Raju Doddapalla, Uma Addepally, Rambabu Gundla, Balaram Patro, Narender Pottabathini

Med.Chem Res. 2015, 24, 2227-2237

Flow Chemistry vs. Batch Processes

Pharmacokinetic Strategies in CNS Drug Discovery

Synthesis of new kojic acid based unnatural ?-amino acid derivatives.

Pd catalyzed C–N Bond Forming Reactions of 6-Bromo-2-cyclopropyl-3-(pyridyl-3-ylmethyl)-4-quinazolin-(3H)-one at Room Temperature

Facile and short synthesis of (+) 1-hydroxy indolizidine and (+) coniceine from picolinic acid ethyl ester via cross claisen condensation

Synthesis, in vitro anticancer and antimycobacterial evaluation of new 5-(2,5-dimethoxyphenyl)-1,3,4-thiadiazole-2-amino derivatives

Mild and General Access to Diverse 1H-Benzotriazoles via Diboron-Mediated N–OH Deoxygenation, and Pd-Catalyzed C–C and C–N Bond Formation

Design, synthesis, and biological evaluation of quinazoline derivatives as a-glucosidase inhibitors

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Flow Chemistry vs. Batch Processes

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Pharmacokinetic Strategies in CNS Drug Discovery

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Publications

Synthesis of new kojic acid based unnatural ?-amino acid derivatives.

Pd catalyzed C–N Bond Forming Reactions of 6-Bromo-2-cyclopropyl-3-(pyridyl-3-ylmethyl)-4-quinazolin-(3H)-one at Room Temperature

Facile and short synthesis of (+) 1-hydroxy indolizidine and (+) coniceine from picolinic acid ethyl ester via cross claisen condensation

Synthesis, in vitro anticancer and antimycobacterial evaluation of new 5-(2,5-dimethoxyphenyl)-1,3,4-thiadiazole-2-amino derivatives

Mild and General Access to Diverse 1H-Benzotriazoles via Diboron-Mediated N–OH Deoxygenation, and Pd-Catalyzed C–C and C–N Bond Formation

Design, synthesis, and biological evaluation of quinazoline derivatives as a-glucosidase inhibitors