A microwave-assisted prepn. of sym. thiazolo[5,4-d]thiazoles from the corresponding aldehydes is presented. The two-step reaction sequence comprises the condensation of aldehydes with dithiooxamide followed by oxidn./aromatization with 1,4-benzoquinone derivs. The new procedure provides the desired products in good yields and in most cases allows redn. of the excess of aldehyde employed in the process compared to previous methodologies. For the first time, application of the reaction both on arom. and aliph. aldehydes is demonstrated.

Microwave-activated synthesis of thiazolo[5,4-d]thiazoles by a condensation/oxidation sequence

Dessi Alessio;Calamante Massimo;Mordini Alessandro;Zani Lorenzo;Reginato Gianna
2014

Abstract

A microwave-assisted prepn. of sym. thiazolo[5,4-d]thiazoles from the corresponding aldehydes is presented. The two-step reaction sequence comprises the condensation of aldehydes with dithiooxamide followed by oxidn./aromatization with 1,4-benzoquinone derivs. The new procedure provides the desired products in good yields and in most cases allows redn. of the excess of aldehyde employed in the process compared to previous methodologies. For the first time, application of the reaction both on arom. and aliph. aldehydes is demonstrated.
2014
Istituto di Chimica dei Composti OrganoMetallici - ICCOM -
Microwave
thiazole
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/247100
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