Strategies for the enantioselective synthesis of spirooxindoles (Q38009722)

26 August 2017

Strategies for the enantioselective synthesis of spirooxindoles (English)

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26 August 2017

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Nicolas R Ball-Jones

1

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PubMed ID

22581310

26 August 2017

Joseph J Badillo

series ordinal

2

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PubMed ID

22581310

26 August 2017

Annaliese K Franz

series ordinal

3

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26 August 2017

14 May 2012

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Organic and Biomolecular Chemistry

26 August 2017

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26 August 2017

10

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26 August 2017

27

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26 August 2017

5165-5181

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Highly enantioselective synthesis and cellular evaluation of spirooxindoles inspired by natural products

26 August 2017

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https://api.crossref.org/works/10.1039%2FC2OB25184A

Luminescent bichromophoric spiroindolones--synthesis and electronic properties.

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC2OB25184A

Spirotryprostatin B, a novel mammalian cell cycle inhibitor produced by Aspergillus fumigatus.

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC2OB25184A

NMR spectra of gelsemine derivatives. The structure and biogenesis of the alkaloid gelsemine

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC2OB25184A

Spirotetrahydro beta-carbolines (spiroindolones): a new class of potent and orally efficacious compounds for the treatment of malaria.

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC2OB25184A

Identification of thiazolidinones spiro-fused to indolin-2-ones as potent and selective inhibitors of the Mycobacterium tuberculosis protein tyrosine phosphatase B.

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC2OB25184A

Oxindole derivatives as orally active potent growth hormone secretagogues.

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC2OB25184A

Pyrrolidinyl-spirooxindole natural products as inspirations for the development of potential therapeutic agents

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC2OB25184A

A library of spirooxindoles based on a stereoselective three-component coupling reaction.

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC2OB25184A

Organocatalytic synthesis of spiro[pyrrolidin-3,3'-oxindoles] with high enantiopurity and structural diversity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC2OB25184A

A unique approach to the concise synthesis of highly optically active spirooxazolines and the discovery of a more potent oxindole-type phytoalexin analogue

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC2OB25184A

Enantioselective construction of spirocyclic oxindolic cyclopentanes by palladium-catalyzed trimethylenemethane-[3+2]-cycloaddition

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC2OB25184A

Core-structure-motivated design of a phosphine-catalyzed [3+2] cycloaddition reaction: enantioselective syntheses of spirocyclopenteneoxindoles.

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC2OB25184A

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC2OB25184A

Targeting structural and stereochemical complexity by organocascade catalysis: construction of spirocyclic oxindoles having multiple stereocenters

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC2OB25184A

Organocatalytic asymmetric formal [4 + 2] cycloaddition for the synthesis of spiro[4-cyclohexanone-1,3'-oxindoline] derivatives in high optical purity

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC2OB25184A

Organocatalytic tandem reaction to construct six-membered spirocyclic oxindoles with multiple chiral centres through a formal [2+2+2] annulation

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC2OB25184A

Asymmetric quadruple aminocatalytic domino reactions to fused carbocycles incorporating a spirooxindole motif

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC2OB25184A

Highly efficient hydrogen-bonding catalysis of the Diels-Alder reaction of 3-vinylindoles and methyleneindolinones provides carbazolespirooxindole skeletons.

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC2OB25184A

Bis-tetrahydrofuran: a privileged ligand for darunavir and a new generation of hiv protease inhibitors that combat drug resistance

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC2OB25184A

Enantioselective synthesis of spirocyclic benzopyranones by rhodium-catalyzed intermolecular [4+2] annulation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC2OB25184A

Catalytic asymmetric [3+2] annulation of allylsilanes with isatins: synthesis of spirooxindoles.

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC2OB25184A

Aspects of Nucleophilic Carbene Chemistry

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC2OB25184A

Organocatalysis by N-heterocyclic carbenes

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC2OB25184A

Highly enantioselective construction of spiro[4H-pyran-3,3'-oxindoles] through a domino Knoevenagel/Michael/cyclization sequence catalyzed by cupreine

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC2OB25184A

Stereoselective synthesis of spirocyclic oxindoles via Prins cyclizations

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC2OB25184A

Enantioselective Pictet-Spengler Reactions of Isatins for the Synthesis of Spiroindolones

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC2OB25184A

Spiroindolones, a potent compound class for the treatment of malaria

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC2OB25184A

Organocatalytic asymmetric synthesis of substituted 3-hydroxy-2-oxindoles via Morita-Baylis-Hillman reaction.

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC2OB25184A

Catalytic asymmetric synthesis of substituted 3-hydroxy-2-oxindoles

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC2OB25184A

Asymmetric addition of indoles to isatins catalysed by bifunctional modified cinchona alkaloid catalysts

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC2OB25184A

Enantioselective and regioselective indium(III)-catalyzed addition of pyrroles to isatins

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC2OB25184A

Catalytic enantioselective stereoablative alkylation of 3-halooxindoles: facile access to oxindoles with C3 all-carbon quaternary stereocenters

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC2OB25184A

The palladium catalyzed asymmetric addition of oxindoles and allenes: an atom-economical versatile method for the construction of chiral indole alkaloids

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC2OB25184A

Asymmetric synthesis of allenyl oxindoles and spirooxindoles by a catalytic enantioselective Saucy-Marbet Claisen rearrangement

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC2OB25184A

An N-heterocyclic carbene/Lewis acid strategy for the stereoselective synthesis of spirooxindole lactones.

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC2OB25184A

Flexible Strategy for Syntheses of Spirooxindoles using Palladium-Catalyzed Carbosilylation and Sakurai-Type Cyclization

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC2OB25184A

Catalytic Asymmetric Synthesis of Oxindoles Bearing a Tetrasubstituted Stereocenter at the C-3 Position

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC2OB25184A

Organocatalytic Michael-alkylation cascade: the enantioselective nitrocyclopropanation of oxindoles

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC2OB25184A

21 January 2018

Identifiers

DOI

10.1039/C2OB25184A

1 reference

26 August 2017

1 reference

PubMed ID

22581310