Synthesis of 1,2,4-Triazolo[4,3-a]pyridines and Related Heterocycles by Sequential Condensation and Iodine-Mediated Oxidative Cyclization.

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Synthesis of 1,2,4-Triazolo[4,3-a]pyridines and Related Heterocycles by Sequential Condensation and Iodine-Mediated Oxidative Cyclization.

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http://www.wikidata.org/entity/Q51275356

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2016 nî lūn-bûn

@nan

2016年の論文

@ja

2016年学术文章

@wuu

2016年学术文章

@zh

2016年学术文章

@zh-cn

2016年学术文章

@zh-hans

2016年学术文章

@zh-my

2016年学术文章

@zh-sg

2016年學術文章

@yue

2016年學術文章

@zh-hant

name

Synthesis of 1,2,4-Triazolo[4, ...... ediated Oxidative Cyclization.

@en

Synthesis of 1,2,4-Triazolo[4, ...... ediated Oxidative Cyclization.

@nl

type

Item

label

Synthesis of 1,2,4-Triazolo[4, ...... ediated Oxidative Cyclization.

@en

Synthesis of 1,2,4-Triazolo[4, ...... ediated Oxidative Cyclization.

@nl

prefLabel

Synthesis of 1,2,4-Triazolo[4, ...... ediated Oxidative Cyclization.

@en

Synthesis of 1,2,4-Triazolo[4, ...... ediated Oxidative Cyclization.

@nl

P1476

Synthesis of 1,2,4-Triazolo[4, ...... Mediated Oxidative Cyclization

@en

P2093

Ertong Li

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

Junbiao Chang

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

Lina Song

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

Zhiyuan Hu

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P2860

Novel triazolopyridylbenzamides as potent and selective p38α inhibitors

Preclinical pharmacokinetics and metabolism of 6-(4-(2,5-difluorophenyl)oxazol-5-yl)-3-isopropyl-[1,2,4]-triazolo[4,3-a]pyridine, a novel and selective p38alpha inhibitor: identification of an active metabolite in preclinical species and human liver

Discovery of 3-cyclopropylmethyl-7-(4-phenylpiperidin-1-yl)-8-trifluoromethyl[1,2,4]triazolo[4,3-a]pyridine (JNJ-42153605): a positive allosteric modulator of the metabotropic glutamate 2 receptor.

Palladium-catalyzed chemoselective monoarylation of hydrazides for the synthesis of [1,2,4]triazolo[4,3-a]pyridines.

1,2,4-triazolo[3,4-a]pyridine as a novel, constrained template for fibrinogen receptor (GPIIb/IIIa) antagonists.

Hypervalent iodine mediated synthesis of 1-aryl/hetryl-1,2,4-triazolo[4,3-a] pyridines and 1-aryl/hetryl 5-methyl-1,2,4-triazolo[4,3-a]quinolines as antibacterial agents.

A straightforward, one-pot protocol for the synthesis of fused 3-aminotriazoles.

Potent 1,3,4-trisubstituted pyrrolidine CCR5 receptor antagonists: effects of fused heterocycles on antiviral activity and pharmacokinetic properties.

Theoretical and experimental design of atypical kinase inhibitors: application to p38 MAP kinase.

4-Amino[1,2,4]triazolo[4,3-a]quinoxalines. A novel class of potent adenosine receptor antagonists and potential rapid-onset antidepressants.

P304

11022-11027

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P31

scholarly article

P356

10.1002/CHEM.201601744

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P407

English

P433

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

P478

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

P50

Wenquan Yu

P577

2016-06-29T00:00:00Z

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P698

27355559

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