Font Size: a A A
Keyword [oxindoles]
Result: 21 - 40 | Page: 2 of 6
21. Studies On Free-radical Initiated C-C(P) Bond Formations Via Selective Csp3-H(P-H) Functionalization
22. The Synthetic Methods Of Several Fluorinated Bioactive Compounds
23. Study On The Tandem Reactions Of Alkenes For The Synthesis Of Cyclic Compounds
24. Cycloaddition Reactions Of Alkynes And 1,2-Difunctiotnalizations Of N-Aryl Acrylamides
25. The Direct Asymmetric Mannich Reaction Of Isatin Imines
26. The Efficient Synthesis Of Oxindole And Its Derivatives
27. Investigation On The Asymmetric Organocatalytic [5+1]Double Michael Addition Reactions
28. The Synthesis Of3-Hydroxy-2-Oxindoles And Diaryl Ethers
29. Facile Synthesis Of Azaarene-Substituted3-Hydroxy-2-Oxindoles Via Lewis/Bronsted Acid-Catalyzed Sp~3C-H Functionalization
30. Studies On Catalytic Asymmetric Synthesis Of Chiral Oxindole Derivatives
31. Organocatalytic Asymmetric Conjugate Addition Of3-Aryloxindoles To Vinyl Bisphosphonate Ester And Preliminary Investigation On The Addition Reaction Of Isocyanoacetate To Trifluoromethyl-Substituted Enones
32. The N-heterocyclic Carbene-palladium(Ⅱ)-1-methylimidazole Complex Catalyzed α-arylation Of Ketones
33. Synthesis Of N-F Reagents And Their Applications On The Enantioselective Fluorination Of Oxindoles
34. Studies On Cycloaddition Reactions Involving Methyleneindolinone
35. The Addition, Cyclization And Rearrangement Of Functionalized Olefins And Their Derivatives
36. Reaction Studies On Construction Of Core Framework Oriented Chiral Centers And Phosphine-Catalyzed Asymmetric [3+2] Cycloaddition
37. Silver-Mediated Radical Fluorination And Trifluoromethylthiolation
38. Asymmetric Synthesis Of Oxindoles And Chroman Derivatives With A Quaternary Center Via Organocatalytic Cascade Reactions
39. The Development Of New Methods For The Synthesis Of Quaternary Oxindoles Featuring A C3All-carbon Or N-containing Carbon Center
40. The Synthesis Of NFSI Analogues And Enantioselective Fluorination Of Oxindoles
  <<First  <Prev  Next>  Last>>  Jump to