353 results on '"Wu, Yan‐Dong"'
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2. I2-DMSO mediated N1/C5 difunctionalization of anthranils with aryl methyl ketones: A facile access to multicarbonyl compounds
3. Improved Ellipse Fitting Algorithm with Outlier Removal
4. Synthesis of 6-oxa-Spiro[4.5]decane Derivatives by Merging Ring-Opening of Benzo[c]oxepines and Formal 1,2-Oxygen Migration.
5. I2‑Induced Umpolung: Synthesis of a 1,6-Dihydrofuro[3,2‑b]pyrazolo[3,4‑e][1,4]thiazine Skeleton via an Unconventional 1,4-Dithiane-2,5-diol Reaction Mode.
6. Divergent synthesis of pyrrolidone fused pyrimido[1,2-b]indazole through selective trapping of an enone intermediate by 1H-indazol-3-amine.
7. I2–DMSO‐Mediated Multicomponent [2+1+1+1] Annulation Reaction via Ethyl Nitroacetate C—NO2 Bond Cleavage as a C1 Synthon: A Route to Multisubstituted β‐Pyrrolidinones Derivatives with a Quaternary Center.
8. Synthesis of β,β-Dithioketones by Merging C–C and C–S Bond Cleavage in [1 + 1 + 1 + 1 + 1 + 1] Annulation
9. Transition-Metal-Free Allylic Defluorination Cross-Electrophile Coupling Employing Rongalite
10. Intramolecular/Intermolecular Sequential Cyclization Accompanied by Double C–F Bond Cleavage: Access to Tricyclic Fluorine-Containing Pyrano[3,2-c]chromenes
11. Difluorocarbene-Enabled Trifluoromethylation and Cyclization for the Synthesis of 3-(Trifluoromethyl)-4H-pyrans
12. I2-Induced Umpolung: Synthesis of a 1,6-Dihydrofuro[3,2-b]pyrazolo[3,4-e][1,4]thiazine Skeleton via an Unconventional 1,4-Dithiane-2,5-diol Reaction Mode
13. Transition‐Metal‐Free Allylic Defluorination Cross‐Electrophile Coupling Employing Rongalite.
14. I2-DMSO-Mediated Construction of 2,3- and 2,4-Disubstituted Pyrimido[1,2-b]indazole Skeletons
15. Base-controlled Selective Cleavage of C−F Bond of Difluorocarbene for the Divergent Assembly of Indolizines
16. Precise diagnosis of three top cancers using dbGaP data
17. I2‑DMSO-Mediated Construction of 2,3- and 2,4-Disubstituted Pyrimido[1,2‑b]indazole Skeletons.
18. Rongalite as a Versatile Reagent in Organic Synthesis†
19. Iodine-promoted five-component reaction using fragment assembly strategy to construct dihydrooxepines
20. I2-DMSO-Mediated Transannulation of Benzo[d]isoxazol-3-amine: Direct Access to 2,4,5-Substituted Pyrimidine Derivatives
21. One Stone, Three Birds: One-Pot Synthesis of Pyrido[3,2-a]phenoxazin-5-one Derivatives from o-Aminophenols with Triple Roles, Paraformaldehyde, and Enaminones via the Povarov Reaction
22. Quadruple C-H activation coupled to hydrofunctionalization and C-H silylation/borylation enabled by weakly coordinated palladium catalyst
23. Rongalite as a Versatile Reagent in Organic Synthesis†.
24. I2-Promoted gem-Diarylethene Involved Aza-Diels–Alder Reaction and Wagner–Meerwein Rearrangement: Construction of 2,3,4-Trisubstituted Pyrimido[1,2-b]indazole Skeletons
25. Direct Hydrodefluorination of CF3-Alkenes via a Mild SN2′ Process Using Rongalite as a Masked Proton Reagent
26. Base-promoted domino reaction for the synthesis of 2,3-disubstituted indoles from 2-aminobenzaldehyde/2-amino aryl ketones, tosylhydrazine, and aromatic aldehydes
27. Direct Introduction of −OCD3 into the Hantzsch Pyrrole Synthesis via Multicomponent Cascade Cyclization: Synthesis of Fully Substituted Pyrrole Derivatives.
28. A Pummerer Reaction-Enabled Modular Synthesis of Alkyl Quinoline-3-carboxylates and 3-Arylquinolines from Amino Acids
29. Synthesis of the Macrolactone Cores of Maltepolides via a Diene–Ene Ring-Closing Metathesis Strategy
30. I2–DMSO mediated multicomponent convergent synthesis of imidazo[2,1-a]isoquinoline derivatives via a triple in situ cross-trapping strategy
31. Aniline Assisted Dimerization of Phenylalanines: Convenient Synthesis of 2-Aroyl-3-arylquinoline in I2-DMSO System
32. I2-DMSO mediated dual α,β-C(sp2)-H functionalization/bicyclization of o-hydroxyphenyl enaminones to construct C2, C3-disubstituted chromone derivatives: chromeno[2,3-b]pyrrol-4(1H)-ones
33. I2-promoted formal [3+1+1+1] cyclization to construct 5-cyano-1H-pyrazolo[3,4-b]pyridine using malononitrile as a C1 synthon
34. I2-DMSO Mediated Multicomponent [3+2] Annulation Reaction: An Approach to Pyrrolo[2,1-a]isoquinoline Derivatives with a Quaternary Center
35. I2-Promoted In Situ Cyclization–Rethiolation Reaction: Synthesis of 2-Aliphatic- or Aromatic-Substituted Indolizines
36. One-Pot Synthesis of Diaryl 1,2-Diketones via Zn-Mediated Reductive Coupling
37. Synthesis of Tetrahydro-2H-thiopyran 1,1-Dioxides via [1+1+1+1+1+1] Annulation: An Unconventional Usage of a Tethered C–S Synthon
38. I2‑DMSO-Mediated Transannulation of Benzo[d]isoxazol-3-amine: Direct Access to 2,4,5-Substituted Pyrimidine Derivatives.
39. Pd-Catalyzed Hydroxyl-Directed Cascade Hydroarylation/C–H Germylation of Nonterminal Alkenes and Aryl Iodides
40. Iodine-Mediated Multicomponent Cascade Cyclization and Sulfenylation/Selenation: Synthesis of Imidazo[2,1-a]isoquinoline Derivatives
41. I2‑Promoted gem-Diarylethene Involved Aza-Diels–Alder Reaction and Wagner–Meerwein Rearrangement: Construction of 2,3,4-Trisubstituted Pyrimido[1,2‑b]indazole Skeletons.
42. Direct Hydrodefluorination of CF3‑Alkenes via a Mild SN2′ Process Using Rongalite as a Masked Proton Reagent.
43. I2-DMSO-Mediated N–H/α-C(sp3)–H Difunctionalization of Tetrahydroisoquinoline: Formal [2 + 2 + 1] Annulation for the Construction of Pyrrolo[2,1-a]isoquinoline Derivatives
44. Successive Promotion of Formal [3+2] Cycloaddition of Aryl Methyl Ketones by I2and Zn: Access to 2-Hydroxy-4-morpholin-2,5-diarylfuran-3(2H)-ones with a Quaternary Carbon Center
45. I2-Promoted site-selective C–C bond cleavage of aryl methyl ketones as C1 synthons for constructing 5-acyl-1H-pyrazolo[3,4-b]pyridines
46. One-step synthesis of azepino[3,4-b]indoles by cooperative aza-[4 + 3] cycloaddition from readily available feedstocks
47. Rongalite as C1 Synthon and Sulfone Source: A Practical Sulfonylmethylation Based on the Separate-Embedding Strategy
48. I2/CuCl2-Copromoted Formal [4 + 1 + 1] Cyclization of Methyl Ketones, 2-Aminobenzonitriles, and Ammonium Acetate: Direct Access to 2-Acyl-4-aminoquinazolines
49. Copper-Catalyzed Oxidative C(sp3)–H/C(sp3)–H Cross-Coupling Reaction of 3-Methylbenzo[c]isoxazoles with Methyl Ketones: Access to Indigoid Analogues
50. Synthesis of the Macrolactone Cores of Maltepolides via a Diene–Ene Ring-Closing Metathesis Strategy
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