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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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Chem Sci
Päätekijät: Ji, Peng, Zhang, Yueteng, Gao, Feng, Bi, Fangchao, Wang, Wei
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: The Royal Society of Chemistry 2020
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC8163235/
https://ncbi.nlm.nih.gov/pubmed/34094490
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1039/d0sc04136j
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