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

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]

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;
2006

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
English
Diels-Alder reaction (Diels-Alder cycloaddn. reactions of 3-aminoisothiazole S,S-dioxides with dimethylbutadiene, cyclopentadiene and furan)
Settore CHIM/06 - Chimica Organica
Articolo
Sì, ma tipo non specificato
2006
Wiley-VCH
2006
18
4285
4290
Pubblicato
Periodico con rilevanza internazionale
AN 2006:994365
info:eu-repo/semantics/article
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]
none
Prodotti della ricerca::01 - Articolo su periodico
6
262
Article (author)
si
F. Clerici, A. Casoni, M.L. Gelmi, D. Nava, S. Pellegrino, A. Sala
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/24093
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