Thiazolylketol Acetates as Glycosyl Donors: Stereoselective Synthesis of a <i>C</i>-Ketoside
We have already proven that thiazolylketol acetates, synthetised by addition of 2-lithiothiazole to sugar lactones followed by acetylation, are efficient glycosyl donors in the presence of <i>O</i>-, <i>N</i>-, and <i>P</i>-nucleophiles. We describe here their first use in the C-glycosidation using...
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| Autori principali: | , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
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MDPI AG
2024-09-01
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| Serie: | Molbank |
| Soggetti: | |
| Accesso online: | https://www.mdpi.com/1422-8599/2024/3/M1883 |
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