A new and efficient synthesis of fully substituted 2,5-dihydrothiophenes by a sequential one-pot four component reaction between primary amines, -ketoesters, aryl isothiocyanates and 1,2-diaza-1,3-dienes (DDs) is reported. A careful selection of the starting materials enables the choice up to six different variations in the architecture of the final products. Furthermore, the acidic treatment of the so obtained 2,5-dihydrothiophenes furnishes the corresponding 5-amino thiophene-2,4-dicarboxylates.

Assembly of Fully Substituted 2,5-Dihydrothiophenes via a Novel Sequential Multicomponent Reaction.

G. Mari;L. De Crescentini;F. Mantellini
Conceptualization
;
S. Santeusanio;G. Favi
2018

Abstract

A new and efficient synthesis of fully substituted 2,5-dihydrothiophenes by a sequential one-pot four component reaction between primary amines, -ketoesters, aryl isothiocyanates and 1,2-diaza-1,3-dienes (DDs) is reported. A careful selection of the starting materials enables the choice up to six different variations in the architecture of the final products. Furthermore, the acidic treatment of the so obtained 2,5-dihydrothiophenes furnishes the corresponding 5-amino thiophene-2,4-dicarboxylates.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11576/2660386
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