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- 1P1: CURRENT APPLICATIONS OF ALDOL CONDENSATION IN BIOORGANIC AND MEDICINAL CHEMISTRY
- 1P2: INTRODUCTION
- 1P3: a) Application of the aldol condensation for the synthesis of diaryl-3-hydroxy-2,3,3a,10a-tetrahydrobenzo[b]cycylopenta[e]azepine-4,10(1H,5H)-diones
- 1P4: b) Synthesis of tetrasubstitutedbicyclo[3.2.1]octenes as potential inhibitors of influenza virus sialidase
- 1P5: c) Thiophilic ring-opening and rearrangement reactions of epoxyketone natural products
- 1P6: d) Integrated synthesis of dihydroacetone phosphate from Glycerol and its utilization in situ for diastereoselective aldol additions
- 1P7: e) Structure-based mutagenesis approaches toward expanding the substrate specificity of D-2-deoxyribose-5-phosphate aldolase
- 1P8: f) Stereoselective allyl transfer to chiral α-methoxycarbaldehydes
- 1P9: g) Synthesis of cationic β-vinyl substituted meso-tetraphenylporphyrins
- 1P10: h) Synthesis of versatile route to arylthiomethyl morpholine analogues of reboxetine
- 1P11: i) Intramolecular aldol cyclization of L-lyxo-Hexos-5-ulose Derivatives
- 1P12: j) Sequential aldol condensation for the synthesis of new glycine antagonists
- 1P13: k) Synthesis and anti-influenza virus activity of 4-guanidino-7-substituted neu5Ac2en derivatives
- 1P14: l) Synthesis and biological evaluations of condensed pyridine and condensed pyrimidine-based HMG-CoA reductase inhibitors
- 1P15: m) Design and biological evaluation of a series of thiophene-based 3-hydroxy-3-methylglutaryl coenzyme a reductase inhibitors
- 1P16: n) 1, 3-Iminoketones as new synthons for the stereocontrolled preparation of useful carbapenem intermediates
- 1P17: o) Synthesis of novel flavonoids using aldol condensation a key step
- 1P18: p) Synthesis and antitumoral, antiviral evaluation of chiral spiropyrans
- 1P19: q) Chemical and Enzymatic Synthesis of Fructose Analogues
- 1P20: r) Synthesis and Biological Evaluations of Quinoline-based HMG-CoA Reductase Inhibitors
- 1P21: s) Synthesis of chaetomellic acids and analogues
- 1P22: t) Synthesis of sialyl Lewis x mimetics as selectin inhibitors by enzymatic aldol condensation reactions
- 1P23: u) Synthesis of 2, 5-linked pyrrolinones
- 1P24: v) Asymmetric aldol condensation as a route to polypropionate derived pheromones
- 1P25: w) Vasodilating and antiarrhythmic activity of heteryl lactones
- 1P26: x) Synthesis of vanillin ethers from 4-(bromomethyl) coumarins as anti-inflammatory agents
- 1P27: y) Synthesis of highly potent benzodiazepine γ-secretase inhibitors
- 1P28: z) Design, synthesis and in vitro testing of α-methylacyl-CoA racemase inhibitors
- 1P29: Conclusion
- Aldol Reaction/condensation