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Direct, stereoselective thioglycosylation enabled by an organophotoredox radical strategy
While strategies involving a 2e(−) transfer pathway have dictated glycosylation development, the direct glycosylation of readily accessible glycosyl donors as radical precursors is particularly appealing because of high radical anomeric selectivity and atom- and step-economy. However, the developmen...
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
The Royal Society of Chemistry
2020
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8163235/ https://www.ncbi.nlm.nih.gov/pubmed/34094490 http://dx.doi.org/10.1039/d0sc04136j |