Quinidine thiourea-catalyzed aldol reaction of unactivated ketones: highly enantioselective synthesis of 3-alkyl-3-hydroxyindolin-2-ones.
about
Asymmetric Aldol Reaction of 3-Acetyl-2H-chromen-2-ones and Isatins Catalyzed by a Bifunctional Quinidine Urea CatalystAcetylphosphonate as a surrogate of acetate or acetamide in organocatalyzed enantioselective aldol reactions.Highly enantioselective three-component direct Mannich reactions of unfunctionalized ketones catalyzed by bifunctional organocatalysts.Developing novel organocatalyzed aldol reactions for the enantioselective synthesis of biologically active molecules.Recent advances in organocatalytic methods for the synthesis of disubstituted 2- and 3-indolinones.Recent advances in organocatalytic methods for asymmetric C-C bond formation.Organocatalytic enantioselective tandem aldol-cyclization reaction of α-isothiocyanato imides and activated carbonyl compoundsAcetaldehyde: A Small Organic Molecule with Big Impact on Organocatalytic Reactions.Organocatalyzed asymmetric Michael reaction of β-aryl-α-ketophosphonates and nitroalkenes.Organocatalyzed enantioselective aldol reaction of 1H-pyrrole-2,3-dionesFacile creation of 3-substituted-3-hydroxy-2-oxindoles by arginine-catalyzed aldol reactions of α,β-unsaturated ketones with isatins.Highly enantioselective construction of 3-hydroxy oxindoles through a decarboxylative aldol addition of trifluoromethyl α-fluorinated gem-diols to N-benzyl isatins.Formal (4+1) Cycloaddition and Enantioselective Michael-Henry Cascade Reactions To Synthesize Spiro[4,5]decanes and Spirooxindole Polycycles.Catalyst-free synthesis of α1-oxindole-α-hydroxyphosphonates via phospha-aldol reaction of isatins employing N-heterocyclic phosphine (NHP)-thiourea.Autoxidation/Aldol Tandem Reaction of 2-Oxindoles with Ketones: A Green Approach for the Synthesis of 3-Hydroxy-2-Oxindoles.Organocatalytic asymmetric synthesis of 3-difluoroalkyl 3-hydroxyoxindoles.Catalytic asymmetric addition of alkyl enol ethers to 1,2-dicarbonyl compounds: highly enantioselective synthesis of substituted 3-alkyl-3-hydroxyoxindoles.Catalytic enantioselective quick route to aldol-tethered 1,6- and 1,7-enynes from ω-unsaturated aldehydes.Cross-Aldol Reaction of Isatin with Acetone Catalyzed by Leucinol: A Mechanistic Investigation.An unprecedented protocol for the synthesis of 3-hydroxy-3-phenacyloxindole derivatives with indolin-2-ones and α-substituted ketones.Fluorous chiral bisoxazolines: application in copper-catalyzed asymmetric α-hydrophosphonylation.Me-BIPAM for the Synthesis of Optically Active 3-Aryl-3-hydroxy-2-oxindoles by Ruthenium-catalyzed Addition of Arylboronic Acids to IsatinsFormal (4+1) Cycloaddition and Enantioselective Michael-Henry Cascade Reactions To Synthesize Spiro[4,5]decanes and Spirooxindole PolycyclesReaction-Based Mechanistic Investigations of Asymmetric Hetero-Diels-Alder Reactions of Enones with Isatins Catalyzed by Amine-Based Three-Component Catalyst SystemsCatalytic asymmetric hetero-Diels–Alder reactions of enones with isatins to access functionalized spirooxindole tetrahydropyrans: scope, derivatization, and discovery of bioactivesSynthesis of Furanose Spirooxindoles via 1,8-Diazabicyclo[5.4.0]undec-7-ene (DBU)-Catalyzed Aldol Reactions of a Pyruvic Aldehyde DerivativeOrganocatalytic asymmetric Henry reaction of isatins: Highly enantioselective synthesis of 3-hydroxy-2-oxindolesHighly stereoselective construction of adjacent tetrasubstituted carbon stereogenic centres via an organocatalytic Mukaiyama-aldol reaction of monofluorinated silyl enol ethers to isatinsCatalytic Asymmetric Construction of Stereogenic Carbon Centers that Feature agem-Difluoroalkyl GroupOrganocatalytic Asymmetric α-Amination of Unprotected 3-Aryl and 3-Aliphatic Substituted Oxindoles using Di-tert-butyl AzodicarboxylateCinchona alkaloid-based phosphoramide catalyzed highly enantioselective Michael addition of unprotected 3-substituted oxindoles to nitroolefins
P2860
Q33604148-F2C54C1B-9E34-43CD-9A57-375EE37BAA69Q36185939-50C965B2-9705-47BA-9CCC-4EE274B58035Q36617922-8ADB6992-02C4-4CB3-84BA-6BDD455B2B02Q37932392-44643780-18E4-49D5-A55E-9375D8E560FFQ38035220-26E7D39F-41C6-4AB4-9E6D-4D12ECCDBC79Q38151648-715D3374-6E81-4E17-92FE-C84FD2B901ABQ38374056-1A9E20CD-AF1A-473B-B743-F139847D6C6AQ38669460-3B181B67-D93E-400E-B337-EF8C6F729627Q41848898-8252E976-D093-4ED9-815C-58C6350E18F9Q41890549-56E080F7-B72D-497A-BDB9-5A0F0E9C9C32Q44024692-C2AAA656-E14B-4A8B-AB1C-A346B05547C4Q45053479-5D66ECCD-5653-4A24-A82C-E6455A8F0685Q48291556-4EDF3DF9-670F-4305-8F49-DF5B3B60C530Q48311310-84444161-805B-4DE0-8407-3CE027FF8DDDQ50236274-FE6F3109-2E55-469F-96F0-EA7F49C5D2B4Q50504697-A612229E-E7B4-4FF4-A541-BC88CD97D2DAQ50525704-903E1C32-7265-457E-A025-BF0E6FBE708BQ51046793-F6219D87-E426-409E-BBE0-03CF1E248DBDQ51578651-0D4532BB-BEDA-46C4-9B76-AC82AD0B13BDQ51603159-109B5244-3E28-4177-9BAE-0EA9754E1F5CQ53509707-C7660DB1-5393-401A-8933-2B740BFDAEDEQ57713734-12A4EE89-0D1E-460C-B58B-D794AD3EEAF0Q57844088-0910E583-761C-495F-8130-326624F26448Q57844097-310D3F27-7529-4D92-B62C-1CE56B04B87CQ57844101-85694DC4-0708-4B03-9DA4-A7B847959541Q57844133-22B370C3-5DFF-448D-8C9D-B6F7371690BAQ57937892-9A5EB77C-6D1F-4BE4-8696-9C3FC9E8E49CQ58172837-1DE7FA96-0A85-4F37-B301-19A5ED4D3285Q58172887-690326F0-5D28-4464-B882-26CB72F791BBQ58172991-5AD515F2-7058-4237-9912-7D436EDF3F16Q58173003-40A81725-1C3E-48AC-A47E-7A7518A2AFE9
P2860
Quinidine thiourea-catalyzed aldol reaction of unactivated ketones: highly enantioselective synthesis of 3-alkyl-3-hydroxyindolin-2-ones.
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
2010年论文
@zh
2010年论文
@zh-cn
name
Quinidine thiourea-catalyzed a ...... alkyl-3-hydroxyindolin-2-ones.
@en
Quinidine thiourea-catalyzed a ...... alkyl-3-hydroxyindolin-2-ones.
@nl
type
label
Quinidine thiourea-catalyzed a ...... alkyl-3-hydroxyindolin-2-ones.
@en
Quinidine thiourea-catalyzed a ...... alkyl-3-hydroxyindolin-2-ones.
@nl
prefLabel
Quinidine thiourea-catalyzed a ...... alkyl-3-hydroxyindolin-2-ones.
@en
Quinidine thiourea-catalyzed a ...... alkyl-3-hydroxyindolin-2-ones.
@nl
P2093
P2860
P356
P1476
Quinidine thiourea-catalyzed a ...... alkyl-3-hydroxyindolin-2-ones.
@en
P2093
Cong-Gui Zhao
Mayur Bhanushali
Qunsheng Guo
P2860
P304
P356
10.1002/ANIE.201004161
P407
P577
2010-12-01T00:00:00Z