3-Amino-substituted isothiazole S,S-dioxides as dienophiles in Diels-Alder cycloaddition reactions with cyclic, acyclic and heterocyclic dienes
Articolo
Data di Pubblicazione:
2006
Citazione:
3-Amino-substituted isothiazole S,S-dioxides as dienophiles in Diels-Alder cycloaddition reactions with cyclic, acyclic and heterocyclic dienes / F. Clerici, A. Casoni, M.L. Gelmi, D. Nava, S. Pellegrino, A. Sala. - In: EUROPEAN JOURNAL OF ORGANIC CHEMISTRY. - ISSN 1434-193X. - 2006:18(2006), pp. 4285-4290. [10.1002/ejoc.200600369]
Abstract:
The Diels-Alder reactions of two 3-aminoisothiazole S,S-dioxides with various dienes, such as 2,3-dimethylbutadiene, cyclopentadiene or furan, under diverse reaction conditions are investigated. Differences of reactivity and selectivity between the studied isothiazoles and the influence of the reaction conditions on the outcome of the reactions are discussed
Tipologia IRIS:
01 - Articolo su periodico
Keywords:
Diels-Alder reaction (Diels-Alder cycloaddn. reactions of 3-aminoisothiazole S,S-dioxides with dimethylbutadiene, cyclopentadiene and furan)
Elenco autori:
F. Clerici, A. Casoni, M.L. Gelmi, D. Nava, S. Pellegrino, A. Sala
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