Design and Synthesis of β-Carboline Based Therapeutically Potential Molecular Architectures via Exploration of Chemselectivity of Aldo-X Bifunctional Building Blocks (AXB3s
Other
Agency: Council of Scientific and Industrial ResearchRole: Principal InvestigatorGrant: 02(0356)/19/EMR-II
Development of New Platform for A3-Coupling and other Multicomponent Reactions towards Drug-Like Molecules using Transition Metal Catalysis
Other
Role: Principal InvestigatorGrant: EMR/2017/000155
Natural Product Inspired Design, Synthesis, and Anticancer Evaluation of β-Carboline Derivatives
Completed
Agency: Council of Scientific and Industrial ResearchRole: Principal InvestigatorGrant: 02(0202)/14/EMR-II
Application of Building Blocks from Morita-Baylis-Hillman Chemistry for the Synthesis of Privileged Scaffolds
Completed
Agency: Department of Science and TechnologyRole: Principal InvestigatorGrant: SB/FT/CS-188/2011
Design and Synthesis of Indole and Pyrazole Fused Biologically Active Frameworks
UniversityDr B R Ambedkar National Institute of Technology, Jalandhar
Year2018
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Natural Product Inspired Design and Synthesis of Biologically Active Indole and β-Carboline Derivatives
UniversityDr B R Ambedkar National Institute of Technology, Jalandhar
Year2019
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Scholarly Publications
Natural Product Inspired Designing and Synthesis of β-Carboline and γ-Lactones Based Molecular Hybrids.
Journal Article
Studies toward the construction of substituted piperidine-2-ones and pyridine-2-ones from Baylis-Hillman adducts: discovery of a facile synthesis of 5-methyl-4-oxo-6-aryl-3-aza-bicyclo[3.1.0]hexane-1-carboxylates
Authors: Singh, V.; Yadav, G.P.; Maulik, P.R.; Batra, S.
An alternate approach to quinoline architecture via Baylis-Hillman chemistry: SnCl<sub>2</sub>-mediated tandem reaction toward synthesis of 4-(substituted vinyl)-quinolines
An alternate approach to quinoline architectire via Baylis-Hillman chemistry: SnCl2-mediated tandem reaction toward synthesis of 4-(substituted vinyl)-quinolines.
Straight forward strategy for stereoselective synthesis of spiro-fused (C-5)isoxazolino or (C-3)pyrazolino-(C-3)-quinolin-2-ones from Baylis-Hillman adducts via 1,3-dipolar cycloaddition and reductive cyclization.
Journal Article
Year: 2008.
Straightforward strategy for the stereoselective synthesis of spiro-fused (C-5)isoxazolino- or (C-3)pyrazolino-(C-3)quinolin-2-ones from Baylis-Hillman adducts by 1,3-dipolar cycloaddition and reductive cyclization
Synthesis of substituted 3-methylene-2-pyridones from Baylis-Hillman derivatives and its application for the generation of 2-pyridone substituted spiroisoxazolines