B. Yogi Sreenivas - Concepedia

Author

B. Yogi Sreenivas

Institute of Life Sciences

Also Known As

B Sreenivas, B. Yogi Sreenivas, Bapu Sreenivas, Dr. Lokesh Ravi, Sreenivas, B. Yogi, Sreenivas, B.Y.

Publications

361

Citations

H-Index

Concepts

All Affiliations

Institute of Life Sciences University of Hyderabad Krishna University Indian Institute of Science Education and Research Kolkata Koneru Lakshmaiah Education Foundation

About

B. Yogi Sreenivas is an author at Institute of Life Sciences specializing in pharmacology, natural sciences, and medicinal chemistry.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Natural Sciences	8	8	259
2	Medicine	6	6	169
3	Biomolecular Engineering	4	4	94
4	Biochemistry	3	3	150
5	Engineering	2	2	47

B. Yogi Sreenivas

Publications

344

Citations

H-Index

Page 1

	Year	Citations
Ultrasound-based approach to spiro-2,3-dihydroquinazolin-4(1H)-ones: their in vitro evaluation against chorismate mutase D. Rambabu, Sarvesh Kumar, B. Yogi Sreenivas, Tetrahedron Letters Medicinal ChemistryChorismate MutaseUltrasound-based ApproachBiochemistryNatural Sciences	2012	66
Spiro heterocycles as potential inhibitors of SIRT1: Pd/C-mediated synthesis of novel N-indolylmethyl spiroindoline-3,2′-quinazolines D. Rambabu, Guttikonda Raja, B. Yogi Sreenivas, Bioorganic & Medicinal Chemistry Letters Novel N-indolylmethyl Spiroindoline-3,2′-quinazolinesMedicinal ChemistryBiochemistryMedicineSpiro Heterocycles	2013	52
Rivastigmine and metabolite analogues with putative Alzheimer’s disease-modifying properties in a Caenorhabditis elegans model Satish N. Dighe, E. De la Mora, Stephen Chan, Communications Chemistry	2019	34
Conformationally restricted functionalized heteroaromatics: a direct access to novel indoloindoles via Pd-mediated reaction Bagineni Prasad, B. Yogi Sreenivas, D. Rambabu, Chemical Communications Novel IndoloindolesOrganic ChemistryChemistryHeterocycle ChemistryPharmaceutical Chemistry	2013	32
C–C bond formation at C-2 of a quinoline ring: Synthesis of 2-(1H-indol-3-yl)quinoline-3-carbonitrile derivatives as a new class of PDE4 inhibitors K. Shiva Kumar, Sarvesh Kumar, B. Yogi Sreenivas, Bioorganic & Medicinal Chemistry Pde4 InhibitorsMedicinal ChemistryNatural SciencesOrganic ChemistryC–c Bond Formation	2012	28
Catalysis by Amberlyst-15 under ultrasound in water: a green synthesis of 1,2,4-benzothiadiazine-1,1-dioxides and their spiro derivatives Sarvesh Kumar, D. Rambabu, C. H. Vijay Kumar, RSC Advances Room TemperatureChemical EngineeringEngineeringSpiro DerivativesSpiro Group	2013	27
A Pd-catalyzed direct entry to 11-substituted 6H-isoindolo[2,1-a]indol-6-one derivatives as potential anticancer agents Suresh Babu Nallapati, Raju Adepu, Mohd Ashraf Ashfaq, RSC Advances Medicinal ChemistryDerivative (Chemistry)DerivativesNatural SciencesMedicine	2015	25
1,2,3-Triazoles derived from olanzapine: their synthesis via an ultrasound assisted CuAAC method and evaluation as inhibitors of PDE4B Suresh Babu Nallapati, B. Yogi Sreenivas, Ramudu Bankala, RSC Advances Molecular PharmacologyMedicinal ChemistryMedicinePharmacological AgentPharmacotherapy	2015	24
Apparent Carbon Monoxide Insertion <i>via</i> Double Isocyanide Incorporation during Palladium‐Catalyzed Construction of Indoloquinoline Ring in a Single Pot: Synthesis of New Cytotoxic Agents Suresh Babu Nallapati, Bagineni Prasad, B. Yogi Sreenivas, Advanced Synthesis & Catalysis Single PotEnantioselective SynthesisDerivativesEngineeringNatural Sciences	2016	20
A Pd-based regioselective strategy to indole-1,2-fused 8- and 9-membered rings: their evaluation as potential scaffolds for apoptosis in zebrafish Bagineni Prasad, B. Yogi Sreenivas, Araka Sushma, Organic & Biomolecular Chemistry Combinatorial ChemistryBioorganic ChemistryPd-based Regioselective StrategyApoptosisMolecular Biology	2014	19

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