Water has proved to be an excellent reaction medium for the definition of highly chemically-efficient and environmentallyfriendly synthetic processes. In several cases, by exploiting the unique properties of water it has been possible to realize more selective and efficient processes than those performed in organic media, including the ring-opening of epoxides by nucleophiles. In this review article the role of water in influencing the stereoselectivity of epoxide ring-opening reactions will be presented, including the most recent examples of enzyme-catalyzed processes.



Titolo: Stereoselective Ring-Opening Reactions of Epoxides in Water
Autori: 
BONOLLO, SIMONA
LANARI, DANIELA
MARROCCHI, Assunta
VACCARO, Luigi
Data di pubblicazione: 2011
Rivista: 
CURRENT ORGANIC SYNTHESIS  
Abstract: Water has proved to be an excellent reaction medium for the definition of highly chemically-efficient and environmentallyfriendly synthetic processes. In several cases, by exploiting the unique properties of water it has been possible to realize more selective and efficient processes than those performed in organic media, including the ring-opening of epoxides by nucleophiles. In this review article the role of water in influencing the stereoselectivity of epoxide ring-opening reactions will be presented, including the most recent examples of enzyme-catalyzed processes.
Handle: http://hdl.handle.net/11391/367095
Appare nelle tipologie:1.1 Articolo in rivista

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