Diguanidinocalix[4]arenes as effective and selective catalysts of the cleavage of diribonucleoside monophosphates
Author:
Affiliation:
1. Dipartimento di Chimica and IMC – CNR Sezione Meccanismi di Reazione
2. Università La Sapienza
3. 00185 Roma, Italy
4. Dipartimento di Chimica
5. Università degli Studi di Parma
6. 43124 Parma, Italy
Abstract
Upper rim diguanidino-cone-calix[4]arenes catalyze the hydrolytic cleavage of diribonucleoside monophosphates in aqueous DMSO with good substrate selectivity and rate accelerations approaching 105-fold in the most favourable substrate-catalyst combinations.
Publisher
Royal Society of Chemistry (RSC)
Subject
General Chemical Engineering,General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2014/RA/C4RA05751A
Reference46 articles.
1. Degrees of Difficulty of Water-Consuming Reactions in the Absence of Enzymes
2. Dinuclear metallo-phosphodiesterase models: application of calix[4]arenes as molecular scaffolds
3. Synthetic metallonucleases for RNA cleavage
4. Di- and Trinuclear Zn2+ Complexes of Calix[4]arene Based Ligands as Catalysts of Acyl and Phosphoryl Transfer Reactions
5. Catalysis of Diribonucleoside Monophosphate Cleavage by Water Soluble Copper(II) Complexes of Calix[4]arene Based Nitrogen Ligands
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