## Abstract The self‐complementary tetrameric propargyl triols **8, 14, 18**, and **21** were synthesized to investigate the duplex formation of self‐complementary, ethynylene‐linked UUAA, AAUU, UAUA, and AUAU analogues with integrated bases and backbone (ONIBs). The linear synthesis is based on re
Oligonucleotide Analogues with Integrated Bases and Backbone. Part 13. Synthesis and Association of Ethynylene-Linked Self-Complementary Dimers.
✍ Scribed by Xiaomin Zhang; Bruno Bernet; Andrea Vasella
- Publisher
- John Wiley and Sons
- Year
- 2007
- Weight
- 11 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0931-7597
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The self-complementary, ethylene-linked U\*[c a ]A ( \* ) dinucleotide analogues 8, 10, 12, 14, 16, and 18, and the sequence-isomeric A\*[c a ]U ( \* ) analogues 20, 22, 24, 26, 28, and 30 were obtained by Pd/Ccatalyzed hydrogenation of the corresponding, known ethynylene-linked dimers. The associat
The self-complementary (Z)-configured U\*[c e ]A ( \* ) dinucleotide analogues 6, 8, 10, 12, 14, and 16, and the A\*[c e ]U ( \* ) dimers 19, 21, 23, 25, 27, and 29 were prepared by partial hydrogenation of the corresponding ethynylene linked dimers. Photolysis of 14 led to the (E)-alkene 17. These
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