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Synthesis of sulfamide linked dinucleotide analogues

✍ Scribed by Jason Micklefield; Kevin J. Fettes


Publisher
Elsevier Science
Year
1997
Tongue
French
Weight
220 KB
Volume
38
Category
Article
ISSN
0040-4039

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✦ Synopsis


Novel sulfamide [-NHSO2NH-] linked dinucleotide analogues d(TnsnT) and d(TnsnA) have been synthesised from 3"--and 5"-amino nucleosides. Treatment of these amino nucleosides with catechol sulfate results in the formation of 2-hydroxyphenyl sulfamate esters which couple smoothly in good yields with either 5"--or 3"-amines of similar nucleosides. NMR studies showed that the 3"sulfamide group results in a preferential C3"--endo (Northern) sugar conformation.


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