3-Aminoisothiazol S-oxides: Reactivity in Diels Alder Cycloaddition ReactionWe studied the Diels Alder cycloaddition reaction of 3-aminoisothiazole S oxides substituted or not at 4 position. The isothiazole system appeared to be an efficient dienophile giving the cycloaddition products in good yields and in a short time. A eco-friendly protocol under microwave conditions with benign solvent or without is presented.
3-Aminoisothiazol S-oxides : Reactivity in Diels Alder Cycloaddition Reaction / F. Clerici, C. Monzani, A. Sala. ((Intervento presentato al 1. convegno Austrian-German-Italian Meeting of Organic Chemistry, tenutosi a Wien nel 2005.
3-Aminoisothiazol S-oxides : Reactivity in Diels Alder Cycloaddition Reaction
F. ClericiPrimo
;
2005
Abstract
3-Aminoisothiazol S-oxides: Reactivity in Diels Alder Cycloaddition ReactionWe studied the Diels Alder cycloaddition reaction of 3-aminoisothiazole S oxides substituted or not at 4 position. The isothiazole system appeared to be an efficient dienophile giving the cycloaddition products in good yields and in a short time. A eco-friendly protocol under microwave conditions with benign solvent or without is presented.
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