Bis- and trisuracil nucleosides with nucleobases anchored to 11-, 12-, and 16-membered macrocyclic scaffolds: Synthesis and aggregation study
Metadata of CSIR Papers
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Title |
Bis- and trisuracil nucleosides with nucleobases anchored to 11-, 12-, and 16-membered macrocyclic scaffolds: Synthesis and aggregation study
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Creator |
Sengupta, J
Mukhopadhyay, R Bhattacharjya, A |
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Subject |
Chemistry, Organic
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Description |
Bis- and trisuracil nucleosides, in which the nucleobases are anchored to isoxazoline ring-fused 11-, 12-, and 16-membered macrooxacycles, were synthesized by nucleosidation of 1,2-isopropylidenefuranose ring-fused macrocycles. The nucleosides exhibited spherical and fiber-like morphologies in water. In one case, the morphology was significantly altered by complexation with an adenine nucleoside via complementary base pairing.
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Publisher |
AMER CHEMICAL SOCWASHINGTON1155 16TH ST, NW, WASHINGTON, DC 20036 USA
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Date |
2011-09-20T12:12:35Z
2011-09-20T12:12:35Z 2007 |
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Type |
Article
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Identifier |
JOURNAL OF ORGANIC CHEMISTRY
0022-3263 http://hdl.handle.net/123456789/14330 |
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Language |
English
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