Organocatalytic Access to Enantioenriched Spirooxindole-Based 4-Methyleneazetidines.

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Organocatalytic Access to Enantioenriched Spirooxindole-Based 4-Methyleneazetidines.

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http://www.wikidata.org/entity/Q48262875

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2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年学术文章

@wuu

2017年学术文章

@zh

2017年学术文章

@zh-cn

2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

@yue

2017年學術文章

@zh-hant

name

Organocatalytic Access to Enantioenriched Spirooxindole-Based 4-Methyleneazetidines.

@en

Organocatalytic Access to Enantioenriched Spirooxindole-Based 4-Methyleneazetidines.

@nl

type

Item

label

Organocatalytic Access to Enantioenriched Spirooxindole-Based 4-Methyleneazetidines.

@en

Organocatalytic Access to Enantioenriched Spirooxindole-Based 4-Methyleneazetidines.

@nl

prefLabel

Organocatalytic Access to Enantioenriched Spirooxindole-Based 4-Methyleneazetidines.

@en

Organocatalytic Access to Enantioenriched Spirooxindole-Based 4-Methyleneazetidines.

@nl

P1476

Organocatalytic Access to Enantioenriched Spirooxindole-Based 4-Methyleneazetidines

@en

P2093

Claudia Spatti

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

Giordano Lesma

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

P2860

Therapeutic Potential of Spirooxindoles as Antiviral Agents

Lead-oriented synthesis: Investigation of organolithium-mediated routes to 3-D scaffolds and 3-D shape analysis of a virtual lead-like library.

Organocatalytic Asymmetric Biginelli-like Reaction Involving Isatin.

Isatins as privileged molecules in design and synthesis of spiro-fused cyclic frameworks.

Spirooxindoles: Promising scaffolds for anticancer agents.

The use of spirocyclic scaffolds in drug discovery.

Evaluation and synthesis of polar aryl- and heteroaryl spiroazetidine-piperidine acetamides as ghrelin inverse agonists.

Pd(II)-Catalyzed Asymmetric Addition of Arylboronic Acids to Isatin-Derived Ketimines.

A catalytic asymmetric construction of a tetrahydroquinoline-based spirooxindole framework via a diastereo- and enantioselective decarboxylative [4+2] cycloaddition.

The utilization of spirocyclic scaffolds in novel drug discovery.

P31

scholarly article

P356

10.3390/MOLECULES22112016

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

P407

English

P433

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

P478

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

P50

Alessandra Silvani

Giulia Rainoldi

M Faltracco

P577

2017-11-21T00:00:00Z

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

P698

29160827

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

P932

6150293

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