Rohan T. Ranasinghe, David A Rusling, Vicki E. C. Powers
May 16, 2005
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0
Influential Citations
42
Citations
Journal
Chemical communications
Abstract
Substituted 3H-pyrrolo[2,3-d]pyrimidin-2(7H)-one nucleoside analogues have been synthesised from 5-alkynyl-uridine derivatives, incorporated into triplex forming oligonucleotides (TFOs) and found to selectively bind CG inversions with enhanced affinity compared to T.