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Decarboxylation of 6-nitrobenzisoxazole-3-carboxylate ion in dichloromethane: The possible role of reverse micelles

โœ Scribed by Raimondo Germani; Pier Paolo Ponti; Nicoletta Spreti; Gianfranco Savelli; Antonio Cipiani; Giorgio Cerichelli; Clifford A Bunton; Victoria Si


Publisher
Elsevier Science
Year
1990
Tongue
English
Weight
584 KB
Volume
138
Category
Article
ISSN
0021-9797

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๐Ÿ“œ SIMILAR VOLUMES


Decarboxylation of 6-Nitrobenzisoxazole-
โœ Pietro Di Profio; Raimondo Germani; Gianfranco Savelli; Nicoletta Spreti; Giorgi ๐Ÿ“‚ Article ๐Ÿ“… 1996 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 75 KB

## NOTE Decarboxylation of 6-Nitrobenzisoxazole-3-Carboxylate Ion in Dichloromethane: The Effects of Surfactant Structure ation of 1 is relatively simple; with or without added water bulky groups at the ammonium ion center increase catalysis, probably by making it The spontaneous decarboxylation

Effect of Ethanol on Micellization and o
โœ Lucia Brinchi; Pietro Di Profio; Raimondo Germani; Gianfranco Savelli; Nicoletta ๐Ÿ“‚ Article ๐Ÿ“… 2002 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 135 KB

The effects of ethanol on the critical micellar concentration (cmc) and the rates of decarboxylation of 6-nitrobenzisoxazole-3-carboxylate (6-NBIC) have been investigated in aqueous cationic surfactants of the cetyltrialkylammonium family with bromide [CT(R)ABr], chloride [CT(R)ACl], and nitrate [CT

SN2 Displacement by Bromide Ions in Dich
โœ Lucia Brinchi; Raimondo Germani; Gianfranco Savelli; Nicoletta Spreti ๐Ÿ“‚ Article ๐Ÿ“… 2006 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 127 KB

## Abstract Reverse micellar systems are of interest as reaction media because they are powerful models for biological compartmentalization, enzymatic catalysis and separation of biomolecules. Solutions of ionic surfactants in apolar solvents may contain reverse micelles, but they may also contain