1,3,4-Oxadiazole Derivatives. Optical Properties in Pure and Mixed Solvents.

about

1,3,4-Oxadiazole Derivatives. Optical Properties in Pure and Mixed Solvents.

Item

http://www.wikidata.org/entity/Q38871283

description

2016 nî lūn-bûn

@nan

2016年の論文

@ja

2016年論文

@yue

2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

@zh-mo

2016年論文

@zh-tw

2016年论文

@wuu

2016年论文

@zh

2016年论文

@zh-cn

name

1,3,4-Oxadiazole Derivatives. Optical Properties in Pure and Mixed Solvents.

@en

type

Item

label

1,3,4-Oxadiazole Derivatives. Optical Properties in Pure and Mixed Solvents.

@en

prefLabel

1,3,4-Oxadiazole Derivatives. Optical Properties in Pure and Mixed Solvents.

@en

P1476

1,3,4-Oxadiazole Derivatives. Optical Properties in Pure and Mixed Solvents

@en

P2093

Anton Airinei

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

P2860

New family of polyamine macrocycles containing 2,5-diphenyl[1,3,4]oxadiazole as a signaling unit. Synthesis, acid-base and spectrophotometric properties.

Optical properties of some novel 2,5-disubstituted 1,3,4-oxadiazole derivatives and their application as an efficient cell staining azo dyes.

Synthesis, urease inhibition, antioxidant, antibacterial, and molecular docking studies of 1,3,4-oxadiazole derivatives.

Synthetic approaches and pharmacological activity of 1,3,4-oxadiazoles: a review of the literature from 2000-2012.

Design, Synthesis, and Antitumor Activity of Novel 5-Pyridyl-1,3,4-oxadiazole Derivatives against the Breast Cancer Cell Line MCF-7.

Solvent-dependent turn-on probe for dual monitoring of Ag(+) and Zn(2+) in living biological samples.

Synthesis and in vitro antiproliferative activity of new 1,3,4-oxadiazole derivatives possessing sulfonamide moiety.

Synthesis and biological screening of 5-(alkyl(1H-indol-3-yl))-2-(substituted)-1,3,4-oxadiazoles as antiproliferative and anti-inflammatory agents.

New 2-benzylsulfanyl-nicotinic acid based 1,3,4-oxadiazoles: their synthesis and biological evaluation.

Synthesis and anticancer activity of 5-(3-indolyl)-1,3,4-thiadiazoles.

P2888

s10895-016-1848-6

P304

1617-1635

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

P31

scholarly article

P356

10.1007/S10895-016-1848-6

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

P433

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

P478

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

P50

Mihaela Homocianu

P577

2016-06-20T00:00:00Z

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

P698

27324952

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