Asymmetric α-amination of 3-substituted oxindoles using chiral bifunctional phosphine catalysts

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Novel α-amino acid-derived phase-transfer catalyst application to a highly enantio- and diastereoselective nitro-Mannich reaction.

P2860

Q52855902-043494D2-2F52-44CA-B647-8E9857BB7ABF

P2860

Asymmetric α-amination of 3-substituted oxindoles using chiral bifunctional phosphine catalysts

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http://www.wikidata.org/entity/Q36992096

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2016 nî lūn-bûn

@nan

2016年の論文

@ja

2016年論文

@yue

2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

@zh-mo

2016年論文

@zh-tw

2016年论文

@wuu

2016年论文

@zh

2016年论文

@zh-cn

name

Asymmetric α-amination of 3-su ...... functional phosphine catalysts

@en

type

Item

label

Asymmetric α-amination of 3-su ...... functional phosphine catalysts

@en

prefLabel

Asymmetric α-amination of 3-su ...... functional phosphine catalysts

@en

P1476

Asymmetric α-amination of 3-su ...... functional phosphine catalysts

@en

P2093

Gang Zhao

http://www.w3.org/2001/XMLSchema#string

Gang Zou

http://www.w3.org/2001/XMLSchema#string

Qiao-Wen Jin

http://www.w3.org/2001/XMLSchema#string

You-Ming Huang

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P2860

Phosphine-catalyzed formation of carbon-sulfur bonds: catalytic asymmetric synthesis of gamma-thioesters

Enantioselective [3 + 2] cycloaddition of allenes to acrylates catalyzed by dipeptide-derived phosphines: facile creation of functionalized cyclopentenes containing quaternary stereogenic centers.

aza-Baylis-Hillman reaction.

Asymmetric carbon-carbon bond formation gamma to a carbonyl group: phosphine-catalyzed addition of nitromethane to allenes.

Advances in nucleophilic phosphine catalysis of alkenes, allenes, alkynes, and MBHADs.

Recent contributions from the Baylis-Hillman reaction to organic chemistry.

Enantioselective organocatalytic allylic amination.

Highly enantioselective organocatalytic α-amination reactions of aryl oxindoles: developing designer multifunctional alkaloid catalysts.

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

Phosphine-catalyzed asymmetric synthesis of beta-lactones from arylketoketenes and aromatic aldehydes.

P304

725-731

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P31

scholarly article

P356

10.3762/BJOC.12.72

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

Zhuo Chai

P577

2016-04-15T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

27340464

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P932

4902028

http://www.w3.org/2001/XMLSchema#string

Asymmetric α-amination of 3-substituted oxindoles using chiral bifunctional phosphine catalysts

about

P2860

P2860

Asymmetric α-amination of 3-substituted oxindoles using chiral bifunctional phosphine catalysts

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P478

P50

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P478

P50

P577

P698

P932