76444-17-2Relevant academic research and scientific papers
THE REACTION OF 2-AMINO-2-DEOXYHEXOPYRANOSES WITH ISOCYANATES. SYNTHESIS OF UREAS AND THEIR TRANSFORMATION INTO HETEROCYCLIC DERIVATIVES.
Avalos, Martin,Babiano, Reyes,Cintas, Pedro,Jimenez, Jose L.,Palacios, Juan C.,Valencia, Concepcion
, p. 2655 - 2675 (2007/10/02)
The reactions of 2-amino-2-deoxyglycopyranoses with aryl isocyanates have been investigated in detail and ureas and heterocyclic derivatives are obtained.The mechanism of formation of glycofuranoimidazolidin-2-ones 62 has now become visible, while
Reaction of 2-amino-2-deoxy-D-glucose with aryl and acyl isothiocyanates, and aryl isocyanates: structure of the intermediate products
Guzman, Jose Fernandez-Bolanos,Rodriguez, Salud Garcia,Fernandez-Bolanos, Jose,Dianez, Ma. Jesus,Lopez-Castro, Amparo
, p. 125 - 143 (2007/10/02)
The structure of (4R)-1-aryl-5-hydroxy-4-(D-arabino-tetritol-1-yl)imidazolidine-2-thiones (1-3), obtained by reaction of 2-amino-2-deoxy-D-glucose with aryl isothiocyanates, has been confirmed by 1H- and 13C-n.m.r. spectroscopy.Likewise, the structures of
Synthesis of glycofuranoimidazolidin-2-ones
Gonzalez, Martin Avalos,Moreno, Pedro Cintas,Monterrey, Isabel M. Gomez,Requejo, Jose L. Jimenez,Albarran, Juan C. Palacios,et al.
, p. 1 - 14 (2007/10/02)
Several 2-(3-arylureido)-2-deoxyglycopyranoses (13-16) have been converted into the corresponding 1-aryl-(1,2-dideoxyglycofurano)imidazolidin-2-ones (17-20) by acid-catalyzed cyclization.Acetylation of these compounds gave 1-aryl-(per-O-acetyl-1,2-
