Development of catalytic reactions using water as a solvent

Authors
Citation
K. Manabe, Development of catalytic reactions using water as a solvent, YAKUGAKU ZA, 121(6), 2001, pp. 395-401
Citations number
16
Categorie Soggetti
Pharmacology & Toxicology
Journal title
YAKUGAKU ZASSHI-JOURNAL OF THE PHARMACEUTICAL SOCIETY OF JAPAN
ISSN journal
00316903 → ACNP
Volume
121
Issue
6
Year of publication
2001
Pages
395 - 401
Database
ISI
SICI code
0031-6903(200106)121:6<395:DOCRUW>2.0.ZU;2-J
Abstract
In recent years, organic reactions in aqueous media have attracted much att ention, not only because these reactions eliminate the necessity of vigorou s drying of solvents and substrates, but also because unique reactivity and selectivity are often observed in the aqueous reactions. Furthermore, orga nic reactions in water may lead to the development of environmentally frien dly chemical processes. We have now developed various types of catalytic or ganic reactions in aqueous media. Catalytic asymmetric aldol reactions in a queous media have attained by using rare earth metal triflates and a chiral multi-dentate ligand. Lewis acid catalysis has become feasible in water by using combinations of water-compatible Lewis acidic cations and anionic su rfactants. These new catalysts were found to form stable colloidal dispersi ons and catalyze various reactions in water. Moreover, Bronsted acid- and p alladium-catalyzed reactions in water have also been performed with the aid of surfactants.