By reacting 4,5-unsubstituted isothiazole dioxides with diazoalkanes and nitrile oxides bicyclic pyrazolo[3,4-d]isothiazole and isothiazolo[5,4-d]isoxazole S,S-dioxides were obtained in good yield through a regioselective cycloaddn. reaction. Through cycloaddn. reaction of 3-benzylamino-4-bromo-isothiazole S,S-dioxide labile cycloadducts were formed that underwent in situ dehydrobromination affording the corresponding aromatized compds
Isothiazolo[5,4-d]isoxazole S,S-dioxides and pyrazolo [3,4-d]-isothiazole S,S-dioxides through cycloaddition reaction on 3-benzylaminoisothiazole S,S-dioxides / F. Clerici, M.L. Gelmi, C. Monzani, D. Pocar, A. Sala. - In: JOURNAL OF HETEROCYCLIC CHEMISTRY. - ISSN 0022-152X. - 43:4(2006), pp. 1045-1049.
Isothiazolo[5,4-d]isoxazole S,S-dioxides and pyrazolo [3,4-d]-isothiazole S,S-dioxides through cycloaddition reaction on 3-benzylaminoisothiazole S,S-dioxides
F. Clerici;M.L. Gelmi;C. Monzani;D. Pocar;
2006
Abstract
By reacting 4,5-unsubstituted isothiazole dioxides with diazoalkanes and nitrile oxides bicyclic pyrazolo[3,4-d]isothiazole and isothiazolo[5,4-d]isoxazole S,S-dioxides were obtained in good yield through a regioselective cycloaddn. reaction. Through cycloaddn. reaction of 3-benzylamino-4-bromo-isothiazole S,S-dioxide labile cycloadducts were formed that underwent in situ dehydrobromination affording the corresponding aromatized compdsPubblicazioni consigliate
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