30 results on '"Xiong Li"'
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2. Divergent synthesis of nitrogen heterocycles via H2O-mediated hydride transfer reactions.
3. Fischer's base-triggered formal (3+2) cycloadditions with 3-isothiocyanato oxindoles as acceptor–donor synthons.
4. Regio- and stereoselective synthesis and evaluation of densely functionalized bispiro[oxindole-isoxazole-indandione] hybrids as anticancer agents.
5. Diastereoselective construction of a library of structural bispiro[butyrolactone/valerolactone–pyrrolidine–indanedione] hybrids via 1,3-dipolar cycloaddition reactions.
6. Decarboxylative, Diastereoselective and exo -Selective 1,3-Dipolar Cycloaddition for Diversity-Oriented Construction of Structural Spiro[Butyrolactone–Pyrrolidine–Chromanone] Hybrids.
7. Dienolate‐Mediated, Regioselective C2‐Polarity Reversal of Chromone‐Based Reactants and Their Application in Nucleophilic Strategies.
8. Stereocontrolled construction of six vicinal stereogenic centers on a hexahydroxanthone framework through a formal [2+1+3] annulation.
9. Oxindole‐chromones C3 Synthons Directed Stereocontrolled Construction of Five Contiguous Stereocenters on Spiro[tetrahydrocyclopenta[b]chromanone‐oxindole]s.
10. One-pot multicomponent construction of chromanone-fused pyrrolidinyl spirooxindole collections through a decarboxylative 1,3-dipolar [3 + 2] cycloaddition reaction.
11. Organocatalytic Michael/Michael Cycloaddition Enabled Asymmetric Construction of Hexahydroxanthones with Skeletal Diversity.
12. Molecular hybridization-guided one-pot multicomponent synthesis of chromanone-fused 3,3′-pyrrolidinyl-dispirooxindoles through a 1,3-dipolar cycloaddition reaction.
13. Molecular Hybridization-Guided One-Pot Multicomponent Synthesis of Turmerone Motif-Fused 3,30-Pyrrolidinyl-dispirooxindoles via a 1,3-Dipolar Cycloaddition Reaction.
14. Molecular hybridization-guided 1,3-dipolar cycloaddition reaction enabled pyrimidine-fused spiropyrrolidine oxindoles synthesis as potential anticancer agents.
15. Construction of turmerone motif-fused spiropyrrolidine oxindoles and their biological evaluation for anticancer activities.
16. Three in one: Rational engineering of multifunctional MIL-101-based ionic catalysts for carbon dioxide-epoxide cycloaddition.
17. Construction of Pyrrolidinyl Spirooxindoles via a 1,3-Dipolar Cycloaddition Reaction of ( E )- N -Boc-3-Alkylidene-Indolin-2(3 H )ones with Azomethine Ylides.
18. ChemInform Abstract: Construction of Turmerone Motif-Fused Spiropyrrolidine Oxindoles and Their Biological Evaluation for Anticancer Activities.
19. ChemInform Abstract: Construction of Pyrrolidinyl Spirooxindoles via a 1,3-Dipolar Cycloaddition Reaction of (E)-N-Boc-3-Alkylidene-indolin-2(3H)ones with Azomethine Ylides.
20. ChemInform Abstract: Highly Efficient and Stereocontrolled Construction of 3,3′-Pyrrolidonyl Spirooxindoles via Organocatalytic Domino Michael/Cyclization Reaction.
21. Diversity-oriented one-pot multicomponent synthesis of chromanone-based 3,3′-pyrrolidinyl-spirooxindoles via a 1,3-dipolar cycloaddition reaction.
22. 3-Methyl-4-nitro-5-isatylidenyl-isoxazoles as 1,3-dipolarophiles for synthesis of polycyclic 3,3′-pyrrolidinyl-dispirooxindoles and their biological evaluation for anticancer activities.
23. Rapid, microwave-accelerated synthesis and anti-osteoporosis activities evaluation of Morusin scaffolds and Morusignin L scaffolds.
24. Diversity-oriented one-pot multicomponent synthesis of spirooxindole derivatives and their biological evaluation for anticancer activities.
25. 1,3-Dipolar cycloaddition enabled isoxazole-fused spiropyrrolidine oxindoles syntheses from 3-methyl-4-nitro-5-alkenyl-isoxazoles and azomethine ylides.
26. A facile and efficient synthesis of polycyclic spiropyrrolidine oxindoles bearing mesityl oxide unit via a three-component 1,3-dipolar cycloaddition reaction.
27. A convenient method for synthesis of polyfunctional dihydropyrrole spiro-fused oxindole-2-ones via an organocatalytic tandem Michael/cyclization sequence.
28. Diastereoselective construction of structurally diverse trifluoromethyl bispiro-[oxindole-pyrrolidine-chromanone]s through [3+2] cycloaddition reactions.
29. ChemInform Abstract: 1,3-Dipolar Cycloaddition Enabled Isoxazole-Fused Spiropyrrolidine Oxindoles Syntheses from 3-Methyl-4-nitro-5-alkenyl-isoxazoles and Azomethine Ylides.
30. ChemInform Abstract: A Facile and Efficient Synthesis of Polycyclic Spiropyrrolidine Oxindoles Bearing Mesityl Oxide Unit via a Three-Component 1,3-Dipolar Cycloaddition Reaction.
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