The pseudo-Michael reaction of 1-aryl-4,5-dihydro-1H-imidazol-2-amines with ethyl ethoxymethylenecyanoacetate.

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The pseudo-Michael reaction of 1-aryl-4,5-dihydro-1H-imidazol-2-amines with ethyl ethoxymethylenecyanoacetate.

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2013 nî lūn-bûn

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2013年の論文

@ja

2013年論文

@yue

2013年論文

@zh-hant

2013年論文

@zh-hk

2013年論文

@zh-mo

2013年論文

@zh-tw

2013年论文

@wuu

2013年论文

@zh

2013年论文

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name

The pseudo-Michael reaction of ...... l ethoxymethylenecyanoacetate.

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type

Item

label

The pseudo-Michael reaction of ...... l ethoxymethylenecyanoacetate.

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prefLabel

The pseudo-Michael reaction of ...... l ethoxymethylenecyanoacetate.

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P1476

The pseudo-Michael reaction of ...... l ethoxymethylenecyanoacetate.

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P2093

Jari Sinkkonen

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Kalevi Pihlaja

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Urszula Kijkowska-Murak

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P2860

A short history of SHELX

Systematic structure modifications of imidazo[1,2-a]pyrimidine to reduce metabolism mediated by aldehyde oxidase (AO).

Structure-activity relationship of 2-hydroxy-2-aryl-2,3-dihydro-imidazo[1,2-a]pyrimidinium salts and 2N-substituted 4(5)-aryl-2-amino-1H-imidazoles as inhibitors of biofilm formation by Salmonella Typhimurium and Pseudomonas aeruginosa.

2-(oxadiazolyl)- and 2-(thiazolyl)imidazo[1,2-a]pyrimidines as agonists and inverse agonists at benzodiazepine receptors.

Generation and exploration of new classes of antitubercular agents: The optimization of oxazolines, oxazoles, thiazolines, thiazoles to imidazo[1,2-a]pyridines and isomeric 5,6-fused scaffolds.

Discovery of aryloxy tetramethylcyclobutanes as novel androgen receptor antagonists.

Imidazo[1,2-a]pyrimidines as functionally selective and orally bioavailable GABA(A)alpha2/alpha3 binding site agonists for the treatment of anxiety disorders.

The mutagenic screening of fourteen imidazo compounds using a modified Ames' test.

Synthesis and antifungal activity evaluation of 3-hydroxyimidazo[1,2-a]pyridine and 3-hydroxyimidazo[1,2-a]pyrimidine derivatives.

Synthesis of acyclo-C-nucleosides in the imidazo[1,2-a]pyridine and pyrimidine series as antiviral agents.

P2888

s00706-013-0982-y

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1171-1182

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scholarly article

P356

10.1007/S00706-013-0982-Y

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P433

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P478

144

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P577

2013-05-14T00:00:00Z

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257450465

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26166883

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4495018

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