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ChemInform Abstract: Isothiazoles. Part 5. Cycloaddition Reaction of Nitrile Oxides to 3- Diethylamino-4-(4-methoxyphenyl)-isothiazole 1,1-Dioxide: An Entry to 5-Acyl- and 5-Cyano-isothiazole 1,1-Dioxide Derivatives.

✍ Scribed by F. CLERICI; F. FERRARIS; M. L. GELMI


Book ID
112028978
Publisher
John Wiley and Sons
Year
2010
Weight
31 KB
Volume
27
Category
Article
ISSN
0931-7597

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πŸ“œ SIMILAR VOLUMES


ChemInform Abstract: Isothiazoles. Part
✍ Egle M. Beccalli; Francesca Clerici; Maria Luisa Gelmi πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 33 KB πŸ‘ 2 views

Isothiazoles. Part 9. An Efficient Synthetic Route to 5-Substituted-3-amino-4-arylisothiazole 1,1-Dioxides and Their 4,5-Dihydro Derivatives. -The thiazole dioxide (I) does not react with alcohols, while the derivative (VIII) does not undergo addition with aliphatic and aromatic amines but with the

Isothiazoles. Part IX. An efficient synt
✍ Egle M Beccalli; Francesca Clerici; Maria Luisa Gelmi πŸ“‚ Article πŸ“… 1999 πŸ› Elsevier Science 🌐 French βš– 599 KB

A simple method to introduce an heteroatom substituent at C-5 of isothiazole dioxides is reported. Through Michael addition reaction 5-substituted isothiazole and 4,5-dihydroisothiazole 1,1-dioxides were obtained allowing the preparation of a series of derivatives of special interest for biological