| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5266111 | Tetrahedron Letters | 2012 | 5 Pages |
Abstract
A three-component sequential process consisting in (1) in situ formation of carbodiimides by Staudinger reaction, (2) reaction with 2-(bromomethyl)-3-aryl-2-propenoic acids, and (3) final cyclization of the resulting N-acylurea intermediates in order to obtain the synthesis of an array of N,Nâ²-disubstituted 5-arylidenedihydropyrimidine-2,4-dione under mild conditions is presented.
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Authors
Maria Cristina Bellucci, Alessandro Volonterio,