Application of the Suzuki-Miyaura reaction in the synthesis of flavonoids. - Test2 - elhamkhani - TriplyDB

Application of the Suzuki-Miyaura reaction in the synthesis of flavonoids.

Application of the Suzuki-Miyaura reaction in the synthesis of flavonoids.

http://www.wikidata.org/entity/Q34681469

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Efficient synthesis of eriodictyol from L-tyrosine in Escherichia coli.Isoflavones, their Glycosides and Glycoconjugates. Synthesis and Biological Activity.Chalcone Derivatives: Promising Starting Points for Drug Design.

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P2860

Application of the Suzuki-Miyaura reaction in the synthesis of flavonoids.

http://www.wikidata.org/entity/Q34681469

description

2013 nî lūn-bûn

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2013 թուականի Ապրիլին հրատարակուած գիտական յօդուած

@hyw

2013 թվականի ապրիլին հրատարակված գիտական հոդված

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2013年の論文

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2013年論文

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2013年論文

@zh-hant

2013年論文

@zh-hk

2013年論文

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2013年論文

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2013年论文

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name

Application of the Suzuki-Miyaura reaction in the synthesis of flavonoids.

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Application of the Suzuki-Miyaura reaction in the synthesis of flavonoids.

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Application of the Suzuki-Miyaura reaction in the synthesis of flavonoids.

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type

label

Application of the Suzuki-Miyaura reaction in the synthesis of flavonoids.

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Application of the Suzuki-Miyaura reaction in the synthesis of flavonoids.

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Application of the Suzuki-Miyaura reaction in the synthesis of flavonoids.

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prefLabel

Application of the Suzuki-Miyaura reaction in the synthesis of flavonoids.

@ast

Application of the Suzuki-Miyaura reaction in the synthesis of flavonoids.

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Application of the Suzuki-Miyaura reaction in the synthesis of flavonoids.

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Application of the Suzuki-Miyaura reaction in the synthesis of flavonoids

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Mamoalosi A Selepe

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

Dietary phytoestrogens and health.

Isoflavonoids of the leguminosae.

Prenylated isoflavonoids: Botanical distribution, structures, biological activities and biotechnological studies. An update (1995-2006).

Nickel-catalysed Negishi cross-coupling reactions: scope and mechanisms.

Synthesis and cytotoxicity evaluation of biaryl-based chalcones and their potential in TNFα-induced nuclear factor-κB activation inhibition.

A chrysin analog exhibited strong inhibitory activities against both PGE2 and NO production.

Synthesis and biological evaluation of 4-arylcoumarin analogues of combretastatins. Part 2.

Synthesis and antiprotozoal activity of 4-arylcoumarins.

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F R van Heerden

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