IJ Pharmaceutical Research
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1. Eco-Friendly Microwave-Assisted Synthesis of Fused Pyrimido[4,5-d]Pyrimidine Derivatives via a Catalyst-Free Hantzsch Multicomponent Reaction
- Eid E.M. , et al.
2. Developments in Synthesis Strategies of Spiro-Barbiturate Compounds: A Classified Study
- Magoo D. , et al.
3. Microwave-assisted Synthesis, Molecular Docking Study of Spirofused Heterocycles as Anti-microbial and Anthelmintic Potential
- Das R. , et al.
4. Cyanuric Chloride Mediated One-Pot Three-Component Reaction of Benzoylhydrazinyl-N-Alkyl Acetamide Derivatives as a New Urease Inhibitor Scaffold: Docking Study and Enzyme Inhibitory Activity
- Ghodrati A. , et al.
5. A review of the synthetic strategies toward spirobarbiturate-fused 3- to 7-membered rings
- Bagherinejad A. , et al.
6. Synthesis of 3,4-Dihydropyrimidin(thio)one Containing Scaffold: Biginelli-like Reactions
- Sánchez-Sancho F. , et al.
7. Chitosan-ZnO: An Efficient and Recyclable Polymer Incorporated Hybrid Nanocatalyst to Synthesize Tetrahydrobenzo[b]pyrans and Pyrano[2,3-d]pyrimidinonesunder Microwave Expedition
- Nesaragi A.R. , et al.
8. Urease inhibitory kinetics, molecular docking, SAR and ADME studies of imine analogues
- Qazi S.U. , et al.
9. Catalyst-Free Three-Component Synthesis, Antibacterial, Antifungal, and Docking Studies of Spiroindoline Derivatives
- Vinoth N. , et al.
10. Synthesis of Spirobarbiturate Piperidin-2-one Derivatives via Cascade Aza-Michael/Michael Cyclization Reaction
- Liu X. , et al.
11. A comprehensive review: Bio-potential of barbituric acid and its analogues
- Shafiq N. , et al.
12. Biginelli Reaction: Polymer Supported Catalytic Approaches
- Patil R.V. , et al.
13. A patent update on therapeutic applications of urease inhibitors (2012–2018)
- Hameed A. , et al.
14. Synthesis of spirobarbiturate-pyrrolidinones: Via a domino aza-Michael/SN2 cyclization of barbiturate-derived alkenes with N-alkoxy α-haloamides
- Wang C.C. , et al.
15. Recent applications of barbituric acid in multicomponent reactions
- Mohammadi Ziarani G. , et al.