Building blocks of methyl alpha-D-glucopyranoside possessing free hydroxyl functions in the position 2 or 3 and orthogonal acid-labile protecting groups on the other reacting sites can be conveniently prepared by means of benzophenone dimethyl ketal under very mild experimental conditions. Trityl and diphenylmethoxymethyl groups have been easily built on secondary hydroxyl groups of monosaccharides for the first time. (C) 1999 Elsevier Science Ltd. All rights reserved.
Building blocks of methyl alpha-D-glucopyranoside possessing free hydroxyl functions in the position 2 or 3 and orthogonal acid-labile protecting groups on the other reacting sites can be conveniently prepared by means of benzophenone dimethyl ketal under very mild experimental conditions. Trityl and diphenylmethoxymethyl groups have been easily built on secondary hydroxyl groups of monosaccharides for the first time. (C) 1999 Elsevier Science Ltd. All rights reserved. RI NAPOLI, ANNA/B-5250-2011; Di Donna, Leonardo/D-5707-2011
A simple procedure for the development of acid-labile protecting groups on position 2 and 3 of methyl alpha-D-glucopyranoside
DI DONNA, Leonardo;Napoli A;SICILIANO, Carlo;SINDONA, Giovanni
1999-01-01
Abstract
Building blocks of methyl alpha-D-glucopyranoside possessing free hydroxyl functions in the position 2 or 3 and orthogonal acid-labile protecting groups on the other reacting sites can be conveniently prepared by means of benzophenone dimethyl ketal under very mild experimental conditions. Trityl and diphenylmethoxymethyl groups have been easily built on secondary hydroxyl groups of monosaccharides for the first time. (C) 1999 Elsevier Science Ltd. All rights reserved. RI NAPOLI, ANNA/B-5250-2011; Di Donna, Leonardo/D-5707-2011I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
