A two step synthesis of BzR/GABAergic active flavones via a Wacker-related oxidation.

about

A versatile approach to flavones via a one-pot Pd(II)-catalyzed dehydrogenation/oxidative boron-Heck coupling sequence of chromanones.

P2860

Q53654927-EA496843-0677-43E4-91FF-F01743BEF28E

P2860

A two step synthesis of BzR/GABAergic active flavones via a Wacker-related oxidation.

Item

http://www.wikidata.org/entity/Q41845290

description

2010 nî lūn-bûn

@nan

2010年の論文

@ja

2010年論文

@yue

2010年論文

@zh-hant

2010年論文

@zh-hk

2010年論文

@zh-mo

2010年論文

@zh-tw

2010年论文

@wuu

2010年论文

@zh

2010年论文

@zh-cn

name

A two step synthesis of BzR/GABAergic active flavones via a Wacker-related oxidation.

@en

type

Item

label

A two step synthesis of BzR/GABAergic active flavones via a Wacker-related oxidation.

@en

prefLabel

A two step synthesis of BzR/GABAergic active flavones via a Wacker-related oxidation.

@en

P1476

A two step synthesis of BzR/GABAergic active flavones via a Wacker-related oxidation.

@en

P2093

James M Cook

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

M Shahjahan Kabir

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

Michael Lorenz

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

P2860

PWZ-029, a compound with moderate inverse agonist functional selectivity at GABA(A) receptors containing alpha5 subunits, improves passive, but not active, avoidance learning in rats

Flavonoids as antioxidants.

An updated unified pharmacophore model of the benzodiazepine binding site on gamma-aminobutyric acid(a) receptors: correlation with comparative models.

Cytotoxic constituents of the lichen Diploicia canescens.

Antiseizure activity of novel gamma-aminobutyric acid (A) receptor subtype-selective benzodiazepine analogues in mice and rat models

The mechanism of the Wacker reaction: a tale of two hydroxypalladations.

Selective benzopyranone and pyrimido[2,1-a]isoquinolin-4-one inhibitors of DNA-dependent protein kinase: synthesis, structure-activity studies, and radiosensitization of a human tumor cell line in vitro.

Synthesis, in vitro affinity, and efficacy of a bis 8-ethynyl-4H-imidazo[1,5a]- [1,4]benzodiazepine analogue, the first bivalent alpha5 subtype selective BzR/GABA(A) antagonist.

Commonly occurring plant flavonoids have estrogenic activity.

Triterpenoids and flavonoids from celery (Apium graveolens).

P304

1095

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

P31

scholarly article

P356

10.1016/J.TETLET.2009.12.107

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

P433

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

P478

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

P577

2010-02-01T00:00:00Z

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

P5875

41453458

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

P698

20161661

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

P932

2818993

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

A two step synthesis of BzR/GABAergic active flavones via a Wacker-related oxidation.

about

P2860

P2860

A two step synthesis of BzR/GABAergic active flavones via a Wacker-related oxidation.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P5875

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P5875

P698

P932