Asymmetric synthesis of fully substituted cyclopentane-oxindoles through an organocatalytic triple Michael domino reaction.

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Asymmetric synthesis of cyclopentanes bearing four contiguous stereocenters via an NHC-catalyzed Michael/Michael/esterification domino reaction.An Asymmetric Organocatalytic Quadruple Domino Reaction Employing a Vinylogous Friedel-Crafts/Michael/Michael/Aldol Condensation Sequence.

P2860

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P2860

Asymmetric synthesis of fully substituted cyclopentane-oxindoles through an organocatalytic triple Michael domino reaction.

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2014 nî lūn-bûn

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2014年の論文

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2014年論文

@yue

2014年論文

@zh-hant

2014年論文

@zh-hk

2014年論文

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2014年論文

@zh-tw

2014年论文

@wuu

2014年论文

@zh

2014年论文

@zh-cn

name

Asymmetric synthesis of fully ...... riple Michael domino reaction.

@en

Asymmetric synthesis of fully ...... riple Michael domino reaction.

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type

Item

label

Asymmetric synthesis of fully ...... riple Michael domino reaction.

@en

Asymmetric synthesis of fully ...... riple Michael domino reaction.

@nl

prefLabel

Asymmetric synthesis of fully ...... riple Michael domino reaction.

@en

Asymmetric synthesis of fully ...... riple Michael domino reaction.

@nl

P1476

Asymmetric synthesis of fully ...... triple Michael domino reaction

@en

P2093

Arne R Philipps

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

Dieter Enders

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Gerhard Raabe

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P2860

Asymmetric Organocatalytic Domino Reactions

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Development of cascade reactions for the concise construction of diverse heterocyclic architectures.

Synthesis and structure-activity relationships of 3-aryloxindoles: a new class of calcium-dependent, large conductance potassium (maxi-K) channel openers with neuroprotective properties.

Synthesis and antitumor effect in vitro and in vivo of substituted 1,3-dihydroindole-2-ones.

Structure-based design of spiro-oxindoles as potent, specific small-molecule inhibitors of the MDM2-p53 interaction.

Catalytic asymmetric intramolecular alpha-alkylation of aldehydes.

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

Construction of bispirooxindoles containing three quaternary stereocentres in a cascade using a single multifunctional organocatalyst.

P304

1004-1008

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scholarly article

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10.1002/CHEM.201406047

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English

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P478

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P50

Liang-Hua Zou

P577

2014-12-02T00:00:00Z

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269042181

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25470781

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P932

4648040

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Asymmetric synthesis of fully substituted cyclopentane-oxindoles through an organocatalytic triple Michael domino reaction.

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P2860

P2860

Asymmetric synthesis of fully substituted cyclopentane-oxindoles through an organocatalytic triple Michael domino reaction.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P5875

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P5875

P698

P932