Multinuclear magnetic resonance studies of 2-aryl-1,3,4-thiadiazoles.

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Multinuclear magnetic resonance studies of 2-aryl-1,3,4-thiadiazoles.

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2012 nî lūn-bûn

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2012年の論文

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2012年学术文章

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2012年学术文章

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2012年学术文章

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2012年学术文章

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2012年学术文章

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2012年學術文章

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2012年學術文章

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2012年學術文章

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Multinuclear magnetic resonance studies of 2-aryl-1,3,4-thiadiazoles.

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Multinuclear magnetic resonance studies of 2-aryl-1,3,4-thiadiazoles.

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Multinuclear magnetic resonance studies of 2-aryl-1,3,4-thiadiazoles.

@en

Multinuclear magnetic resonance studies of 2-aryl-1,3,4-thiadiazoles.

@nl

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Multinuclear magnetic resonance studies of 2-aryl-1,3,4-thiadiazoles.

@en

Multinuclear magnetic resonance studies of 2-aryl-1,3,4-thiadiazoles.

@nl

P1476

Multinuclear magnetic resonance studies of 2-aryl-1,3,4-thiadiazoles

@en

P2093

Błażej Gierczyk

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Maciej Zalas

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Marcin Kaźmierczak

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Michał Cegłowski

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P2860

A survey of Hammett substituent constants and resonance and field parameters

Chemotherapy of human African trypanosomiasis.

Inhibition of growth of Leishmania donovani promastigotes by newly synthesized 1,3,4-thiadiazole analogs.

Pro-oxidant and antiproliferative effects of the 1,3,4-thiadiazole-based Schiff base and its metal complexes.

Thiosugar nucleosides. Synthesis and biological activity of 1,3,4-thiadiazole, thiazoline and thiourea derivatives of 5-thio-D-glucose.

Polysubstituted pyrazoles, part 5. Synthesis of new 1-(4-chlorophenyl)-4-hydroxy-1H-pyrazole-3-carboxylic acid hydrazide analogs and some derived ring systems. A novel class of potential antitumor and anti-HCV agents.

Evaluation of new thiadiazoles and benzothiazoles as potential radioprotectors: free radical scavenging activity in vitro and theoretical studies (QSAR, DFT).

Green synthesis and biological evaluation of some novel azoles as antimicrobial agents.

Amino acid derivatives, part 4: synthesis and anti-HIV activity of new naphthalene derivatives.

Synthesis and antileishmanial activity of novel 5-(5-nitrofuran-2-y1)-1,3,4-thiadiazoles with piperazinyl-linked benzamidine substituents.

P304

637-641

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P31

scholarly article

P356

10.1002/MRC.3850

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P433

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P478

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P50

P577

2012-07-31T00:00:00Z

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P698

22847904

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