Abstract
A novel sugar-modified thymidine analogue, 3'-deoxy-4'-C-(2-hydroxyethyl)thymidine (X), was designed and synthesized to show that it can stabilize hairpin structures when it is present in the loop moiety, probably due to the flexibility of the one-carbon-elongated 4'-branched structure.
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APA
Shuto, S., Tamura, Y., Yamamoto, Y., Kodama, T., Hoshika, S., Ichikawa, S., … Matsuda, A. (2004). Stable hairpins having a loop consisting of 3’-deoxy-4’-C-(2-hydroxyethyl)thymidines. Nucleic Acids Symposium Series (2004), (48), 67–68. https://doi.org/10.1093/nass/48.1.67
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