Photodimerizations of hydroxy- and benzoylated 4-azachalcones and quantum chemical investigation of the reactions.

about

Photodimerizations of hydroxy- and benzoylated 4-azachalcones and quantum chemical investigation of the reactions.

Item

http://www.wikidata.org/entity/Q43169523

description

2010 nî lūn-bûn

@nan

2010年の論文

@ja

2010年学术文章

@wuu

2010年学术文章

@zh

2010年学术文章

@zh-cn

2010年学术文章

@zh-hans

2010年学术文章

@zh-my

2010年学术文章

@zh-sg

2010年學術文章

@yue

2010年學術文章

@zh-hant

name

Photodimerizations of hydroxy- ...... nvestigation of the reactions.

@en

Photodimerizations of hydroxy- ...... nvestigation of the reactions.

@nl

type

Item

label

Photodimerizations of hydroxy- ...... nvestigation of the reactions.

@en

Photodimerizations of hydroxy- ...... nvestigation of the reactions.

@nl

prefLabel

Photodimerizations of hydroxy- ...... nvestigation of the reactions.

@en

Photodimerizations of hydroxy- ...... nvestigation of the reactions.

@nl

P1476

Photodimerizations of hydroxy- ...... nvestigation of the reactions.

@en

P2093

Ahmet Yaşar

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

Asu Usta

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

Nuran Yayli

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

Nurettin Yayli

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

P2860

Development of the Colle-Salvetti correlation-energy formula into a functional of the electron density

Inhibition of myeloperoxidase release from rat polymorphonuclear leukocytes by a series of azachalcone derivatives

A new mixing of Hartree–Fock and local density‐functional theories

(Rel)-1beta,2alpha-di-(2,4-dihydroxy-6-methoxybenzoyl)-3beta, 4alpha-di-(4-methoxyphenyl)-cyclobutane and other flavonoids from the aerial parts of Goniothalamus gardneri and Goniothalamus thwaitesii.

Photocyclization of iminyl radicals: theoretical study and photochemical aspects.

Stereoselective synthesis of monomeric flavonoids.

Synthesis and antimicrobial properties of N-substituted derivatives of (E)-4-azachalcones.

Cyclobutanes from Combretum albopunctatum.

Multiorbital interactions during Acyl radical addition reactions involving imines and electron-rich olefins.

P2888

s00894-009-0642-7

P304

1347-1355

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

P31

scholarly article

P356

10.1007/S00894-009-0642-7

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

P433

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

P478

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

P577

2010-02-06T00:00:00Z

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

P5875

41414977

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

P698

20140472

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