An easy and efficient strategy to obtain libraries of 5-phosphodiester and 5-phosphoramidate monoester nucleoside analogues in a highly pure form has been developed, starting from a new nucleoside based solid support. The nucleoside scaffold has been anchored through a 5-phosphodiester linkage to Tentagel® HL resin, functionalized with a 3-chloro-4-hydroxyphenylacetic linker. The solid phase synthesis of small libraries of 5-phosphodiester and 5-phosphoramidate monoester thymidine analogues is also reported.
An efficient solid phase synthesis of 5’-phosphodiester and phosphoramidate monoester nucleoside analogues / DE NAPOLI, Lorenzo; DI FABIO, Giovanni; J., D’Onofrio; Montesarchio, Daniela. - In: CHEMICAL COMMUNICATIONS. - ISSN 1359-7345. - ELETTRONICO. - (2005), pp. 2586-2588. [10.1039/B501043H]
An efficient solid phase synthesis of 5’-phosphodiester and phosphoramidate monoester nucleoside analogues
DE NAPOLI, LORENZO;DI FABIO, GIOVANNI;MONTESARCHIO, DANIELA
2005
Abstract
An easy and efficient strategy to obtain libraries of 5-phosphodiester and 5-phosphoramidate monoester nucleoside analogues in a highly pure form has been developed, starting from a new nucleoside based solid support. The nucleoside scaffold has been anchored through a 5-phosphodiester linkage to Tentagel® HL resin, functionalized with a 3-chloro-4-hydroxyphenylacetic linker. The solid phase synthesis of small libraries of 5-phosphodiester and 5-phosphoramidate monoester thymidine analogues is also reported.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.