Ask any question about EPFL courses, lectures, exercises, research, news, etc. or try the example questions below.
DISCLAIMER: The Graph Chatbot is not programmed to provide explicit or categorical answers to your questions. Rather, it transforms your questions into API requests that are distributed across the various IT services officially administered by EPFL. Its purpose is solely to collect and recommend relevant references to content that you can explore to help you answer your questions.
A method for the facile prepn. of oligoribonucleotide analogs contg. b-D-allo-furanosyl nucleosides with addnl. functional groups tethered to the 6'-O positions is presented. It is based on the synthesis in two protected nucleosides carrying a 6'-O-bromopentyl and a 6'-O-methylaminopentyl substituent. By a simple two-step procedure, these key intermediates were transformed into two phosphoramidites carrying a 1-aza-18-crown-6 and a triethyleneglycol group, resp., each capable of complexing metal ions. By automated synthesis, these functionalized nucleoside analogs were efficiently incorporated into short oligoribonucleotides. Under physiol. conditions (150 mM NaCl, 2 mM MgCl2, pH 7.4), incorporation of a single allo-furanosyl cytosine substituted with a triethyleneglycol moiety led to a significant enthalpic stabilization of an A-type RNA duplex. This observation is in agreement with a metal ion-mediated stabilizing interaction between the two pairing strands. [on SciFinder (R)]