ArticleAngewandte Chemie (International ed. in English)2013
Chemical diversification of sialic acid glycosides by stereospecific, chemoselective deamination.
Article in Angewandte Chemie (International ed. in English), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.
What it found
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Who cites it
11 citing papers in PubMed.
- Syntheses of Legionaminic Acid, Pseudaminic Acid, Acetaminic Acid, 8-Organic letters · 2022Article
- Use of hydroxylamines, hydroxamic acids, oximes and amines as nucleophiles in the Zbiral oxidative deamination of N-acetyl neuraminic acid. Isolation and characterization of novel mono- and disubstitution products.Carbohydrate research · 2020Article
- Use of Phenols as Nucleophiles in the Zbiral Oxidative Deamination ofThe Journal of organic chemistry · 2019Article
- Synthesis of saccharocin from apramycin and evaluation of its ribosomal selectivity.MedChemComm · 2019Article
- Synthesis and Stereocontrolled Equatorially Selective Glycosylation Reactions of a Pseudaminic Acid Donor: Importance of the Side-Chain Conformation and Regioselective Reduction of Azide Protecting Groups.Journal of the American Chemical Society · 2018Article
- Reductive Deamination by Benzyne for Deoxy Sugar Synthesis Through a Domino Reaction.ChemistryOpen · 2017Article
- Stereoselective Synthesis of 5-epi-α-Sialosides Related to the Pseudaminic Acid Glycosides. Reassessment of the Stereoselectivity of the 5-Azido-5-deacetamidosialyl Thioglycosides and Use of Triflate as Nucleophile in the Zbiral Deamination of Sialic Acids.The Journal of organic chemistry · 2016Article
- Oxidative Deamination of N-Acetyl Neuraminic Acid: Substituent Effects and Mechanism.Journal of the American Chemical Society · 2016Article
- The isothiocyanato moiety: an ideal protecting group for the stereoselective synthesis of sialic acid glycosides and subsequent diversification.Angewandte Chemie (International ed. in English) · 2015Article
- Probing the influence of protecting groups on the anomeric equilibrium in sialic acid glycosides with the persistent radical effect.Journal of the American Chemical Society · 2014Article
- Oxidative deamination of amino sugars: recent advances.Carbohydrate chemistry · 1979Article
Corrections and comments
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Authors and funding
2 authors.
Funding
Abstract
Late bloomer: Nitrosation of peracetylated sialic acid glycosides followed by treatment with sodium trifluoroethoxide and then a suitable nucleophile enables the late-stage modification of these glycosides with stereospecific replacement of the acetamido group. This method should enable access to many glycoside derivatives with a minimum of synthetic effort.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.