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Matching Glycosyl Donor Reactivity to Sulfonate Leaving Group Ability Permits S(N)2 Glycosylations
[Image: see text] Here we demonstrate that highly β-selective glycosylation reactions can be achieved when the electronics of a sulfonyl chloride activator and the reactivity of a glycosyl donor hemiacetal are matched. While these reactions are compatible with the acid- and base-sensitive protecting...
Tallennettuna:
| Julkaisussa: | J Am Chem Soc |
|---|---|
| Päätekijät: | , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
American Chemical
Society
2019
|
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6814073/ https://ncbi.nlm.nih.gov/pubmed/31550879 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/jacs.9b07022 |
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