Facile and efficient enantioselective hydroxyamination reaction: synthesis of 3-hydroxyamino-2-oxindoles using nitrosoarenes.
about
Asymmetric Aldol Reaction of 3-Acetyl-2H-chromen-2-ones and Isatins Catalyzed by a Bifunctional Quinidine Urea CatalystAsymmetric catalytic aza-Morita-Baylis-Hillman reaction for the synthesis of 3-substituted-3-aminooxindoles with chiral quaternary carbon centersEnantioselective addition of diphenyl phosphonate to ketimines derived from isatins catalyzed by binaphthyl-modified organocatalystsOrganocatalytic asymmetric Michael addition of unprotected 3-substituted oxindoles to 1,4-naphthoquinoneOrganocatalytic asymmetric allylic amination of Morita-Baylis-Hillman carbonates of isatins.Zn-mediated asymmetric allylation of N-tert-butanesulfinyl ketimines: an efficient and practical access to chiral quaternary 3-aminooxindoles.Chiral scandium(III)-catalyzed enantioselective α-arylation of N-unprotected 3-substituted oxindoles with diaryliodonium salts.Organocatalytic asymmetric cyanation of isatin derived N-Boc ketoimines.Skeletal Rearrangement in the Zn(II) -Catalyzed [4+2]-Annulation of Disubstituted N-Hydroxy Allenylamines with Nitrosoarenes to Yield Substituted 1,2-Oxazinan-3-one Derivatives.Highly enantioselective Michael addition of 3-arylthio- and 3-alkylthiooxindoles to nitroolefins catalyzed by a simple cinchona alkaloid derived phosphoramide.Highly diastereo- and enantioselective Michael addition of 3-substituted benzofuran-2(3H)-ones to 4-oxo-enoates catalyzed by lanthanide(III) complexes.Highly stereoselective conjugate addition and α-alkynylation reaction with electron-deficient alkynes catalyzed by chiral scandium(III) complexes.Catalytic asymmetric cross-dehydrogenative coupling: activation of C-H bonds by a cooperative bimetallic catalyst system.Nickel(II)-catalyzed enantioselective 1,3-dipolar cycloaddition of azomethine imines with alkylidene malonates.Organocatalytic asymmetric synthesis of 3,3-disubstituted oxindoles featuring two heteroatoms at the C3 position.A catalytic asymmetric ring-expansion reaction of isatins and α-alkyl-α-diazoesters: highly efficient synthesis of functionalized 2-quinolone derivatives.A catalytic metal-free Ritter reaction to 3-substituted 3-aminooxindoles.Enantioselective synthesis of β-pyrazole-substituted alcohols through an asymmetric ring-opening reaction of meso-epoxides.Highly Z-selective asymmetric conjugate addition of alkynones with pyrazol-5-ones promoted by N,N'-dioxide-metal complexes.Asymmetric synthesis of tetrahydroquinolines with quaternary stereocenters through the Povarov reaction.Asymmetric synthesis of cis-4-aminobenzopyran derivatives catalyzed by N,N'-dioxide-Sc(OTf)3 complexes.Imidazolylpyridine-In(OTf)3 catalyzed enantioselective allylation of ketimines derived from isatins.Recent advances in cooperative bimetallic asymmetric catalysis: dinuclear Schiff base complexes.Brønsted acid mediated N-O bond cleavage for α-amination of ketones through the aromatic nitroso aldol reaction.Organocatalytic, Asymmetric Synthesis of 3-SulfenylatedN-Boc-Protected OxindolesAn Organocatalytic Addition of Nitromethane to Activated KetiminesOrganocatalytic 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-B31A450B-067A-4B47-A1E3-BC31992F867BQ36662095-ED99F7F3-0B31-4B6D-AA18-651B6F79F224Q37165340-6CCFFA34-05CC-41BC-995C-BDB185A6E93FQ42609518-76BF9355-F91A-46E7-90F3-AEE56953F0DBQ42610880-6A999F6B-124A-4F8C-BC9F-ABA79D5D517DQ43481610-978BF29A-1238-40F9-8391-83535C9970C2Q45227563-D1E3AC44-EF96-4AD2-B019-BAF6431EF629Q45711632-99D94FB8-05BE-4311-AEAB-E235EC76A3F6Q46475858-B0C80FEC-41F6-4353-8EA3-CAA23B3E1921Q50447290-75CB6535-9D98-4F22-9BD9-37B2E8E0A503Q50458222-AE19F781-6691-4D73-87FF-2BAA1F2BB5FCQ50480554-03E5B7D8-1436-4748-BE4A-1C13EC0A14CCQ50482656-6CDCD249-941C-4191-BA2D-6DA88A7A5246Q50483395-433AEF75-CBA0-4889-9BF0-C43D4403E3DDQ50484585-CFC89AAB-02F8-4B28-98EB-957FD51CB669Q50493208-E6DB3897-E86C-4BF8-8359-108751FF5A1DQ50500528-9F6C1494-4CA5-4292-9715-A10ABF08EA61Q50501894-B9872C92-4ADF-4F49-9598-0D38B06DD818Q50503061-B7E09E36-DD99-4A56-BAF5-D073A78D6B52Q50507765-0230CAA6-1B65-4AC3-A9D7-D897E0BDB143Q50508459-24E03B24-0335-456E-9060-72682FC7A596Q51326750-56DCEF11-9BFF-4079-AC9B-D6F0605908ADQ51770110-3518113C-8DB1-4A8B-B9D1-2BC42FA70FC5Q52887333-83FED2B1-78AD-44F4-83D3-010D9689F5FDQ58045504-28146C69-0D14-434E-8500-80B5CB6DCD2BQ58172854-77FF6A53-B64B-4F81-A8A9-78F91EDA7345Q58172991-369EE690-3F3E-40D5-B5DA-C7A99A3509C0Q58173003-30DB2B59-26F3-4B1E-9AAF-4CCFB82AA0D0
P2860
Facile and efficient enantioselective hydroxyamination reaction: synthesis of 3-hydroxyamino-2-oxindoles using nitrosoarenes.
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年学术文章
@wuu
2011年学术文章
@zh
2011年学术文章
@zh-cn
2011年学术文章
@zh-hans
2011年学术文章
@zh-my
2011年学术文章
@zh-sg
2011年學術文章
@yue
2011年學術文章
@zh-hant
name
Facile and efficient enantiose ...... oxindoles using nitrosoarenes.
@en
Facile and efficient enantiose ...... oxindoles using nitrosoarenes.
@nl
type
label
Facile and efficient enantiose ...... oxindoles using nitrosoarenes.
@en
Facile and efficient enantiose ...... oxindoles using nitrosoarenes.
@nl
prefLabel
Facile and efficient enantiose ...... oxindoles using nitrosoarenes.
@en
Facile and efficient enantiose ...... oxindoles using nitrosoarenes.
@nl
P2860
P50
P356
P1476
Facile and efficient enantiose ...... oxindoles using nitrosoarenes.
@en
P2093
P2860
P304
P356
10.1002/ANIE.201100758
P407
P577
2011-04-14T00:00:00Z