(Q43090891)

English

Highly enantioselective synthesis of 3-amino-2-oxindole derivatives: catalytic asymmetric alpha-amination of 3-substituted 2-oxindoles with a chiral scandium complex

scientific article published in June 2010

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Europe PubMed Central

PubMed publication ID

13 November 2017

Highly enantioselective synthesis of 3-amino-2-oxindole derivatives: catalytic asymmetric alpha-amination of 3-substituted 2-oxindoles with a chiral scandium complex (English)

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PubMed publication ID

13 November 2017

enantioselectivity

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based on heuristic

inferred from title

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based on heuristic

inferred from title

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6

object named as

Xiaohua Liu

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13 November 2017

8

object named as

Xiaoming Feng

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13 November 2017

7

object named as

Lili Lin

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13 November 2017

5

object named as

Donghui Chen

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13 November 2017

3

object named as

Sha Bai

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13 November 2017

author name string

Zhigang Yang

1

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13 November 2017

Zhen Wang

2

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13 November 2017

Ke Shen

4

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13 November 2017

language of work or name

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publication date

1 June 2010

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13 November 2017

Chemistry—A European Journal

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13 November 2017

16

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13 November 2017

22

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13 November 2017

6632-6637

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13 November 2017

Asymmetric induction in the Neber rearrangement of simple ketoxime sulfonates under phase-transfer conditions: experimental evidence for the participation of an anionic pathway.

1 reference

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Recent advances in catalytic, enantioselective alpha aminations and alpha oxygenations of carbonyl compounds

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Catalytic asymmetric synthesis of alpha-amino acids.

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Asymmetric catalysis with chiral primary amine-based organocatalysts

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Direct catalytic asymmetric alpha-amination of aldehydes

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Evolution of a synthetic strategy: total synthesis of (+/-)-welwitindolinone A isonitrile

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Cinchona-alkaloid-catalyzed enantioselective direct aldol-type reaction of oxindoles with ethyl trifluoropyruvate

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Asymmetric iminium ion catalysis with a novel bifunctional primary amine thiourea: controlling adjacent quaternary and tertiary stereocenters

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A homodinuclear Mn(III)2-Schiff base complex for catalytic asymmetric 1,4-additions of oxindoles to nitroalkenes.

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Thiourea-catalyzed highly enantio- and diastereoselective additions of oxindoles to nitroolefins: application to the formal synthesis of (+)-physostigmine.

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Enantioselective base-free phase-transfer reaction in water-rich solvent

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Catalytic enantioselective fluorination of oxindoles

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Highly enantioselective catalytic fluorination and chlorination reactions of carbonyl compounds capable of two-point binding.

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Cinchona alkaloid catalyzed enantioselective fluorination of allyl silanes, silyl enol ethers, and oxindoles

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Development of Chiral Nucleophilic Pyridine Catalysts: Applications in Asymmetric Quaternary Carbon Synthesis

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Asymmetric synthesis of pyrrolidinoindolines. Application for the practical total synthesis of (-)-phenserine

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Enantioselective TADMAP-catalyzed carboxyl migration reactions for the synthesis of stereogenic quaternary carbon

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Lewis acid-catalyzed enantioselective hydroxylation reactions of oxindoles and beta-keto esters using DBFOX ligand.

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Mo-catalyzed regio-, diastereo-, and enantioselective allylic alkylation of 3-aryloxindoles

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Enantioselective synthesis of SM-130686 based on the development of asymmetric Cu(I)F catalysis to access 2-oxindoles containing a tetrasubstituted carbon.

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Organocatalytic asymmetric allylic alkylation of oxindoles with Morita-Baylis-Hillman carbonates

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Palladium-catalyzed enantioselective alpha-arylation and alpha-vinylation of oxindoles facilitated by an axially chiral P-stereogenic ligand

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Catalytic double stereoinduction in asymmetric allylic alkylation of oxindoles

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Expanding the scope of cinchona alkaloid-catalyzed enantioselective alpha-aminations of oxindoles: a versatile approach to optically active 3-amino-2-oxindole derivatives

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Asymmetric construction of quaternary stereocenters by direct organocatalytic amination of 3-substituted oxindoles

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Identifiers

10.1002/CHEM.201000126

1 reference

Europe PubMed Central

PubMed publication ID

13 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

13 November 2017

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