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Intramolecular hydrogen bonding guides a cationic amphiphilic organocatalyst to highly stereoselective aldol reactions in water†
Ángel M. Valdivielso,Alba Catot,Ignacio Alfonso,Ciril Jimeno
RSC Advances Pub Date : 07/10/2015 00:00:00 , DOI:10.1039/C5RA12135C
Abstract

A novel amphiphilic guanidine organocatalyst, efficient for asymmetric aldol reactions of ketones in water at neutral pH, is disclosed. The reaction presented a clear substrate dependence depicting a free energy linear correlation with ee. Intramolecular hydrogen bonding in the acylguanidine moiety was identified as the key structural motif.

Graphical abstract: Intramolecular hydrogen bonding guides a cationic amphiphilic organocatalyst to highly stereoselective aldol reactions in water
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