Calix[4]arenes derivatives 1 and 2, featuring two guanidine units at the upper rim, catalyze the transesterification of diribonucleoside monophosphates much more effectively than that of HPNP. Rate accelerations relative to the background range from 10(3) to 10(4)-fold, and approach 10(5)-fold with the most favorable substrate-catalyst combinations.

Salvio, R., Cacciapaglia, R., Mandolini, L., Sansone, F., Casnati, A. (2014). Diguanidinocalix[4]arenes as effective and selective catalysts of the cleavage of diribonucleoside monophosphates. RSC ADVANCES, 4(65), 34412-34416 [10.1039/c4ra05751a].

Diguanidinocalix[4]arenes as effective and selective catalysts of the cleavage of diribonucleoside monophosphates

Salvio R.
;
2014-01-01

Abstract

Calix[4]arenes derivatives 1 and 2, featuring two guanidine units at the upper rim, catalyze the transesterification of diribonucleoside monophosphates much more effectively than that of HPNP. Rate accelerations relative to the background range from 10(3) to 10(4)-fold, and approach 10(5)-fold with the most favorable substrate-catalyst combinations.
2014
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore CHIM/06 - CHIMICA ORGANICA
English
Con Impact Factor ISI
Salvio, R., Cacciapaglia, R., Mandolini, L., Sansone, F., Casnati, A. (2014). Diguanidinocalix[4]arenes as effective and selective catalysts of the cleavage of diribonucleoside monophosphates. RSC ADVANCES, 4(65), 34412-34416 [10.1039/c4ra05751a].
Salvio, R; Cacciapaglia, R; Mandolini, L; Sansone, F; Casnati, A
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/247719
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