Abstract
We reported a remote control glycosylation method using the picoloyl protecting group for 2-deoxy-β-glycosidic bond formation. The method is applicable to various 2-deoxythioglycosyl donors and the utility is illustrated by the synthesis of a deoxytrisaccharide component of landomycins. This journal is
| Original language | English |
|---|---|
| Pages (from-to) | 5394-5397 |
| Number of pages | 4 |
| Journal | Chemical Communications |
| Volume | 51 |
| Issue number | 25 |
| DOIs | |
| State | Published - 28 Mar 2015 |
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Ruei, J. H., Venukumar, P., Ingle, A. B., & Mong, K-K. (2015). C6 picoloyl protection: A remote stereodirecting group for 2-deoxy-β-glycoside formation. Chemical Communications, 51(25), 5394-5397. https://doi.org/10.1039/c4cc08465a