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Keyword [oxindoles]
Result: 41 - 60 | Page: 3 of 6
41. Metal-free Cyclization Via C-H Activation To Form Oxindoles
42. Sythesis Of Oxazoles And Synthesis Of Oxindoles By Tandem Reaction
43. Palladium-catalyzed Asymmetric[3+2] Cycloaddition Reaction Of Vinyl Cyclopropanes And Isatin Derived Imines
44. The Asymmetric Mannich Reaction Of N-Boc C-alkynyl Imines And C3-Substituted Oxindoles
45. Organocatalytic Asymmetric Michael-cyclization Cascade Reaction To Spirocyclicoxindoles Containing Rhodanine Or Thiazolidinediones
46. Study On Allylation Of Indole Ketone Compounds
47. Study On Bifunctional Properties Of Olefins And Alkynes
48. Theoretical Studies On The Three Kinds Of Catalytic Reactions For The Construction Of 3,3-disubstituted Oxindoles
49. Aryldifluoro(chloro)methylation Of Activated Alkenes: Synthesis Of Difluoro(chloro)methyl Oxindoles
50. Study On Difunctionalization Of Unsaturated Amides For The Synthesis Of Oxindoles
51. Synthesis Of Oxindoles Via Cu-mediated ATRA Between N-phenylacrylamides And Ethyl 2-bromo-2-methylpropionate
52. Chiral Phosphoric Acid Catalyzed Alkylation Reaction Of ?-Ketoacids With 3-Hydroxy-3-Substituted Oxindoles
53. Research On The One Pot Synthesis Of Spiro [3,5'-pyrrolo [2,1-?] Isoquinolin-oxindoles]
54. The Organocatalytic Asymmetric Synthesis Of Dihydro-Coumarins And ?,?-Disubstituted Unnatural ?-Amino Ester
55. Synthesis Of Spiropyrazoline Oxindoles By A Formal [4+1] Annulation Reaction Between 3-Bromooxindoles And In Situ-Derived 1,2-Diaza-1,3-Dienes
56. Addition Of Carbamoylsiane To Isation: Synthesisi Of 3-hydroxy-3-aminocarbony-2-oxind Oles Derivatives
57. Catalytic Asymmetric Tandem Conjugate Addition Addition-protonation Reactions To Install Nonadjacent Chiral Secondary Hydroxyl
58. The Direct Construction Of(fused)heterocyclic Structures Via The Functionalization Of Amines With Methyl Ketones Sp~3 C-H Bond
59. Study On The Organocatalyzed Stereoselective Synthesis Of The Spiro [Pyrrolidin-3,3'-oxindoles] Ring
60. Allylation Reaction Of Oxindoles And Its Application
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