| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5276751 | Tetrahedron Letters | 2010 | 5 Pages |
Abstract
A series of 6-aryl-5-(1-cyclohexen-1-yl)pyrrolo[2,3-d]pyrimidines 9a-q were obtained by the three-component reaction between 6-aminopyrimidines 6, 7, 8, dimedone 2, and arylglyoxal 5a,b. The unexpected cyclization process was established by NMR and X-ray diffraction measurements.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
![Generation of pyrrolo[2,3-d]pyrimidines. Unexpected products in the multicomponent reaction of 6-aminopyrimidines, dimedone, and arylglyoxal](/preview/png/5276751.png "First Page Preview: Generation of pyrrolo[2,3-d]pyrimidines. Unexpected products in the multicomponent reaction of 6-aminopyrimidines, dimedone, and arylglyoxal")
Authors
Jairo Quiroga, Paola A. Acosta, Silvia Cruz, Rodrigo AbonÃa, Braulio Insuasty, Manuel Nogueras, Justo Cobo,