Benzyne arylation of oxathiane glycosyl donors
The arylation of bicyclic oxathiane glycosyl donors has been achieved using benzyne generated in situ from 1-aminobenzotriazole (1-ABT) and lead tetraacetate. Following sulfur arylation, glycosylation of acetate ions proceeded with high levels of stereoselectivity to afford α-glycosyl acetates in a...
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| Hauptverfasser: | , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Beilstein-Institut
2010-02-01
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| Schriftenreihe: | Beilstein Journal of Organic Chemistry |
| Schlagworte: | |
| Online-Zugang: | https://doi.org/10.3762/bjoc.6.19 |
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