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ChemInform Abstract: Preparation of Diazenes by Electrophilic C-Coupling Reactions of Dry Arenediazonium o- Benzenedisulfonimides with Grignard Reagents.

โœ Scribed by M. BARBERO; I. DEGANI; S. DUGHERA; R. FOCHI; P. PERRACINO


Publisher
John Wiley and Sons
Year
2010
Weight
32 KB
Volume
29
Category
Article
ISSN
0931-7597

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โœฆ Synopsis


Preparation of Diazenes by Electrophilic C-Coupling Reactions of Dry Arenediazonium o-Benzenedisulfonimides with Grignard Reagents. -Twenty-three different aryldiazenes (III) are prepared by electrophilic C-coupling reactions of highly pure and stable salts (I) with Grignard reagents. Work-up temp. of 30 โ€ข C gives both E-and Z-isomers, whereas heating to 70 โ€ข C for 1 hour results in exclusive formation of the E-isomer. -(BARBERO, M.;


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ChemInform Abstract: A Simple Preparatio
โœ Margherita Barbero; Iacopo Degani; Stefano Dughera; Rita Fochi; Paolo Perracino ๐Ÿ“‚ Article ๐Ÿ“… 2010 ๐Ÿ› John Wiley and Sons โš– 29 KB

A Simple Preparation of Aryl Methanesulfonates by Thermal Decomposition of Dry Arenediazonium o-Benzenedisulfonimides in Methanesulfonic Acid. -The thermal decomposition of the highly stable arenediazonium salts (I) in methanesulfonic acid fails when a methoxy, fluoro or nitro group is in ortho-posi