Glycosylation via remote activation of anomeric leaving groups: development of 2-(2-propylsulfinyl)benzyl glycosides as novel glycosyl donors
Author:
Affiliation:
1. Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation
2. School of Pharmacy
3. Huazhong University of Science and Technology
4. Wuhan
5. China
Abstract
New glycosyl donors with recyclable and regenerable leaving groups, which could be activated via remote mode, were designed for latent-active glycosylation.
Funder
National Natural Science Foundation of China
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2016/QO/C5QO00359H
Reference78 articles.
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2. K. Toshima and K.Sasaki, in Comprehensive Glycoscience, ed. J. P. Karmerling, G.-J. Boons, Y. C. Lee, A. Suzuki, N. Taniguchi and A. G. J. Voragen, Elsevier, Oxford, UK, 2007, pp. 261–311
3. Recent progress in O-glycosylation methods and its application to natural products synthesis
4. Strategies in Oligosaccharide Synthesis
5. Chapter 5 Oligosaccharide Synthesis: From Conventional Methods to Modern Expeditious Strategies
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