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Influence of the 2-aryl group on the ipso electrophilic substitution process of 2-arylimidazo[1,2-a]pyridines

DOI: 10.1515/HC.2008.14.1-2.27

Source and publish data:

Heterocyclic Communications p. 27 - 32 (2008)

Update date:2022-07-30

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Authors:

Salgado-Zamora, HectorSalgado-Zamora, Hector

Velazquez, ManuelVelazquez, Manuel

Mejia, DanielMejia, Daniel

Campos-AldreteCampos-Aldrete

Jimenez, RogelioJimenez, Rogelio

Cervantes, HumbertoCervantes, Humberto

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Article abstract of DOI:10.1515/HC.2008.14.1-2.27

A systematic study of electrophilic substitution reactions of 3-nitroso-2-arylimidazo[1,2-a]pyridine confirmed that the nitroso group may be ipso-substituted by bromine (NBS in DMF) and that bromine in turn may be substituted by the nitroso group. Electro

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Full text of DOI:10.1515/HC.2008.14.1-2.27

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Download Date | 5/27/15 9:12 AM  
Brought to you by | Purdue University Libraries  
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Download Date | 5/27/15 9:12 AM  
Brought to you by | Purdue University Libraries  
Authenticated  
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Download Date | 5/27/15 9:12 AM  
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Products guided by the article

Product name:2-(4'-fluorophenyl)-3-nitrosoimidazo[1,2-a]pyridine

Cas No:1115604-53-9

1115604-53-9

R&D Labs maybe for 1115604-53-9

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