Additive-controlled synthesis of 1- and 2-dexoysugars from thioglycosides
Author:
Affiliation:
1. State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, Beijing, China
2. State Key Laboratory of Pharmaceutical Biotechnology, School of Life Sciences, Nanjing University, Nanjing, China
Funder
National Natural Science Foundation of China
the open fund of State Key Laboratory of Pharmaceutical Biotechnology, Nanjing University, China
Fundamental Research Funds for the Central Universities
Publisher
Informa UK Limited
Subject
Organic Chemistry,Biochemistry
Link
https://www.tandfonline.com/doi/pdf/10.1080/07328303.2021.2015366
Reference38 articles.
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2. Pearce, A. J.; Mallet, J.M.; Sinaÿ, P. 2001. Radicals in Carbohydrate Chemistry; Renaud, P., Sibi, M.P., Eds. Wiley-VCH Verlag GmbH: Weinheim, Germany, 2001. DOI: 10.1002/9783527618293.ch52.
3. Radical C-glycosylation reaction of pyranosides with the 2,3-trans carbamate group
4. First protection-free protocol for synthesis of 1-deoxy sugars through glycosyl dithiocarbamate intermediates
5. Synthesis of Postulated Molecular Probes: Stereoselective Free-Radical-Mediated C-Glycosylation in Tandem with Hydrogen Transfer
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