| Literature DB >> 10866405 |
J Matulic-Adamic1, A T Daniher, A Karpeisky, P Haeberli, D Sweedler, L Beigelman.
Abstract
A series of novel 2'-modified nucleoside 5'-triphosphates was synthesized. The amino, imidazole, and carboxylate functionalities were attached to the 5-position of pyrimidine base of these molecules through alkynyl and alkyl spacers, respectively. Two different phosphorylation methods were used to optimize the yields of these highly modified triphosphates.Entities:
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Year: 2000 PMID: 10866405 DOI: 10.1016/s0960-894x(00)00226-2
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823