ArticleOrganic & biomolecular chemistry2017
OFox imidates as versatile glycosyl donors for chemical glycosylation.
Article in Organic & biomolecular chemistry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
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Who cites it
9 citing papers in PubMed, 17 citations in OpenAlex.
- Synthesis and Glycosidation of Anomeric Halides: Evolution from Early Studies to Modern Methods of the 21st Century.Chemical reviews · 2022Review
- HPLC-Based Automated Synthesis of Glycans in Solution.Chemistry (Weinheim an der Bergstrasse, Germany) · 2022Article
- Recent Advances in Stereoselective ChemicalFrontiers in molecular biosciences · 2022Review
- A Streamlined Regenerative Glycosylation Reaction: Direct, Acid-Free Activation of Thioglycosides.Chemistry (Weinheim an der Bergstrasse, Germany) · 2021Article
- Recent Developments in Stereoselective Chemical Glycosylation.Asian journal of organic chemistry · 2019Article
- Investigation of Glycosyl Nitrates as Building Blocks for Chemical Glycosylation.European journal of organic chemistry · 2018Article
- Automated Chemical Oligosaccharide Synthesis: Novel Approach to Traditional Challenges.Chemical reviews · 2018Review
- The Experimental Evidence in Support of Glycosylation Mechanisms at the SChemical reviews · 2018Review
- Regenerative Glycosylation.The Journal of organic chemistry · 2018Article
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Authors and funding
6 authors at 1 institution in 1 country.
Funding
Abstract
Previously we communicated 3,3-difluoroxindole (HOFox) - mediated glycosylations wherein 3,3-difluoro-3H-indol-2-yl (OFox) imidates were found to be key intermediates. Both the in situ synthesis from the corresponding glycosyl bromides and activation of the OFox imidates could be conducted in a regenerative fashion. Herein, we extend this study with the main focus on the synthesis of various OFox imidates and their investigation as glycosyl donors for chemical 1,2-cis and 1,2-trans glycosylation.
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Registered trials
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