(Q28142967)

English

A convenient extension of the Wessely-Moser rearrangement for the synthesis of substituted alkylaminoflavones as neuroprotective agents in vitro

scientific article (publication date: 17 April 2000)

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scholarly article

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10782697%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

A convenient extension of the Wessely-Moser rearrangement for the synthesis of substituted alkylaminoflavones as neuroprotective agents in vitro (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10782697%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

Martine Largeron

4

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6 November 2019

author name string

R Larget

1

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6 November 2019

B Lockhart

2

1 reference

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6 November 2019

P Renard

3

1 reference

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6 November 2019

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publication date

1 April 2000

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6 November 2019

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4

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Bioorganic & Medicinal Chemistry Letters

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6 November 2019

10

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6 November 2019

835-838

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6 November 2019

8

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6 November 2019

Synthesis of novel orthoalkylaminophenol derivatives as potent neuroprotective agents in vitro.

1 reference

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7 January 2021

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322. Molecular rearrangement of some o-acyloxyacetophenones and the mechanism of the production of 3-acylchromones

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Synthese und Konstitution des Skutellareins

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Selective reduction of aromatic nitro compounds with stannous chloride in non acidic and non aqueous medium

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The Use of Diethyl Azodicarboxylate and Triphenylphosphine in Synthesis and Transformation of Natural Products

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