Synthesis and Triplex Forming Properties of an Acyclic N7-Glycosylated Guanine Nucleoside
摘要:
A chiral acyclic nucleoside, one in which the ribose carbohydrate has been replaced with a glycerol-based linker, is prepared by glycosylating guanine at the N-7-nitrogen. The stereochemically pure derivative is converted to a DMT-protected phosphoramidite for incorporation into DNA sequences. Sequence containing the acyclic N-7-dG nucleoside are capable of forming DNA triplexes in which it is likely that the N-1-H and N-2-amino groups of the N-7-dG are involved in recognition of the guanine base in G-C base pairs.
Synthesis and Triplex Forming Properties of an Acyclic N7-Glycosylated Guanine Nucleoside
摘要:
A chiral acyclic nucleoside, one in which the ribose carbohydrate has been replaced with a glycerol-based linker, is prepared by glycosylating guanine at the N-7-nitrogen. The stereochemically pure derivative is converted to a DMT-protected phosphoramidite for incorporation into DNA sequences. Sequence containing the acyclic N-7-dG nucleoside are capable of forming DNA triplexes in which it is likely that the N-1-H and N-2-amino groups of the N-7-dG are involved in recognition of the guanine base in G-C base pairs.