Synthesis of ganglioside Hp-s1
RSC Advances, ISSN: 2046-2069, Vol: 4, Issue: 88, Page: 47752-47761
2014
- 8Citations
- 6Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Article Description
A simple protocol for the synthesis of a ganglioside Hp-s1 (1) starting from commercially available phytosphingosine, sialic acid, and d-glucose is described. This synthesis involved a glycosylation reaction of a phytosphingosine derived acceptor with a highly active benzyl protected glucosyl donor, a second glycosylation of a glucosyl acceptor with a sialyl donor followed by Staudinger reaction, amidation, and global deprotection as key steps. This journal is
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84907887555&origin=inward; http://dx.doi.org/10.1039/c4ra08272a; http://xlink.rsc.org/?DOI=C4RA08272A; http://pubs.rsc.org/en/content/articlepdf/2014/RA/C4RA08272A; https://xlink.rsc.org/?DOI=C4RA08272A; https://dx.doi.org/10.1039/c4ra08272a; https://pubs.rsc.org/en/content/articlelanding/2014/ra/c4ra08272a
Royal Society of Chemistry (RSC)
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