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On the reaction of 3-nitroimidazo[1,2-a]pyridine-2-carbonitrile with amino acid derivatives

DOI: 10.1515/HC.2009.15.1.73

Source and publish data:

Heterocyclic Communications p. 73 - 78 (2009)

Update date:2022-08-05

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Authors:

Hernandez, JorgeHernandez, Jorge

Salgado-Zamora, HectorSalgado-Zamora, Hector

Cervantes, HumbertoCervantes, Humberto

Arias, LucinaArias, Lucina

Campos, Ma. ElenaCampos, Ma. Elena

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Article abstract of DOI:10.1515/HC.2009.15.1.73

The displacement of the nitrile group in 3-nitroimidazo[l,2-a]pyridine-2- carbonitrile by amino acids led to the preparation of corresponding AMmidazo[l,2-a]pyridine-.N-amino acid derivatives. In the case of amino acid derived bidentated nucleophiles, exp

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Full text of DOI:10.1515/HC.2009.15.1.73

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Brought to you by | University of Arizona  
Authenticated  
Download Date | 5/25/15 8:19 PM  
Brought to you by | University of Arizona  
Authenticated  
Download Date | 5/25/15 8:19 PM  
Brought to you by | University of Arizona  
Authenticated  
Download Date | 5/25/15 8:19 PM  
Brought to you by | University of Arizona  
Authenticated  
Download Date | 5/25/15 8:19 PM  
Brought to you by | University of Arizona  
Authenticated  
Download Date | 5/25/15 8:19 PM  

Products guided by the article

Product name:2-N-(3'-nitroimidazo[1,2-a]pyridin-2-yl)-2-phenylaminoethanol

Cas No:1208112-94-0

1208112-94-0

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