N-Glycosylation with Sulfoxide Donors for the Synthesis of Peptidonucleosides
<p>We report here the synthesis of peptidonucleosides obtained after glycosylation of different pyrimidine bases with glucopyranosyl donors carrying an azide group at the C4 position. A methodological study involving different anomeric leaving groups (acetate, phenylsulfoxide and <i>ortho</i>-hexynylbenzoate) showed that a sulfoxide donor in combination with trimethylsilyl triflate as the promoter led to the best yields.</p>
1972 ◽
Vol 27
(03)
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pp. 610-618
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Keyword(s):
2010 ◽
Vol 33
(11)
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pp. 2202-2210
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