Synthesis and biological activity of the nucleoside analogs based on polyfluoroalkyl-substituted 1,2,3-triazoles.

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Synthesis of new 1,2,3-triazole derivatives of uracil and thymine with potential inhibitory activity against acidic corrosion of steels.

P2860

Q43843069-942B35B8-9400-482E-9467-2FDDC6886CE2

P2860

Synthesis and biological activity of the nucleoside analogs based on polyfluoroalkyl-substituted 1,2,3-triazoles.

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http://www.wikidata.org/entity/Q39464017

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2011 nî lūn-bûn

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2011年の論文

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2011年論文

@yue

2011年論文

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2011年論文

@zh-hk

2011年論文

@zh-mo

2011年論文

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2011年论文

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2011年论文

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2011年论文

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name

Synthesis and biological activ ...... l-substituted 1,2,3-triazoles.

@en

Synthesis and biological activ ...... l-substituted 1,2,3-triazoles.

@nl

type

Item

label

Synthesis and biological activ ...... l-substituted 1,2,3-triazoles.

@en

Synthesis and biological activ ...... l-substituted 1,2,3-triazoles.

@nl

prefLabel

Synthesis and biological activ ...... l-substituted 1,2,3-triazoles.

@en

Synthesis and biological activ ...... l-substituted 1,2,3-triazoles.

@nl

P1476

Synthesis and biological activ ...... yl-substituted 1,2,3-triazoles

@en

P2093

Anna V Golovan

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Ganna P Gudz

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

Nadezhda V Nesterova

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

Oleksandr S Kanishchev

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

Yuriy G Shermolovich

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

P2860

Synthesis of alpha- and beta-D-glucopyranosyl triazoles by CuAAC 'click chemistry': reactant tolerance, reaction rate, product structure and glucosidase inhibitory properties.

Fluorinated nucleosides.

Click chemistry reactions in medicinal chemistry: applications of the 1,3-dipolar cycloaddition between azides and alkynes.

Fluorinated Nucleosides: Synthesis and Biological Implication

Cu(I)-catalyzed Huisgen azide-alkyne 1,3-dipolar cycloaddition reaction in nucleoside, nucleotide, and oligonucleotide chemistry.

A stereoselective intramolecular halo-etherification of chiral enamides in the synthesis of halogenated cyclic ethers.

1,2,3-Triazole-[2',5'-bis-O-(tert-butyldimethylsilyl)-beta-D- ribofuranosyl]-3'-spiro-5"-(4"-amino-1",2"-oxathiole 2",2"-dioxide) (TSAO) analogues: synthesis and anti-HIV-1 activity.

Growth inhibition and induction of cellular differentiation of human myeloid leukemia cells in culture by carbamoyl congeners of ribavirin.

Synthesis of 2'-aminoalkyl-substituted fluorinated nucleobases and their influence on the kinetic properties of hammerhead ribozymes.

beta-1,2,3-Triazolyl-nucleosides as nicotinamide riboside mimics.

P304

768-783

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P31

scholarly article

P356

10.1080/15257770.2011.602654

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P433

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

P478

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

P50

Svetlana D Zagorodnya

P577

2011-10-01T00:00:00Z

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P5875

51689055

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P698

21967288

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Synthesis and biological activity of the nucleoside analogs based on polyfluoroalkyl-substituted 1,2,3-triazoles.

about

P2860

P2860

Synthesis and biological activity of the nucleoside analogs based on polyfluoroalkyl-substituted 1,2,3-triazoles.

description

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type

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P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P5875

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P5875

P698