Jack Porter
3,4,6-Tri-O-acetyl-1-S-acetyl-2-deoxy-2-S-phenylthio-α-d-mannopyranoside
Porter, Jack; Miller, Gavin J.
Abstract
The title compound was isolated as the unexpected reaction product from a reaction attempting to access a glycosyl 1-phosphate. The product was isolated in good yield, as one diastereoisomer, and was characterised by 1H, 13C, and 2D NMR, alongside HRMS analysis.
Citation
Porter, J., & Miller, G. J. (2025). 3,4,6-Tri-O-acetyl-1-S-acetyl-2-deoxy-2-S-phenylthio-α-d-mannopyranoside. Molbank, 2025(1), 1-6. https://doi.org/10.3390/M1981
Journal Article Type | Article |
---|---|
Acceptance Date | Mar 11, 2025 |
Online Publication Date | Mar 17, 2025 |
Publication Date | 2025-03 |
Deposit Date | Apr 3, 2025 |
Journal | Molbank |
Electronic ISSN | 1422-8599 |
Publisher | MDPI |
Peer Reviewed | Peer Reviewed |
Volume | 2025 |
Issue | 1 |
Article Number | M1981 |
Pages | 1-6 |
DOI | https://doi.org/10.3390/M1981 |
Keywords | mannose, thioglycoside, sulphur, glycoside, NMR |
Public URL | https://keele-repository.worktribe.com/output/1112765 |
You might also like
Fluorinated nucleosides, nucleotides and sugar nucleotides
(2023)
Journal Article
Synthesis of 4-thio-d-glucopyranose and interconversion to 4-thio-d-glucofuranose.
(2023)
Journal Article
Downloadable Citations
About Keele Repository
Administrator e-mail: research.openaccess@keele.ac.uk
This application uses the following open-source libraries:
SheetJS Community Edition
Apache License Version 2.0 (http://www.apache.org/licenses/)
PDF.js
Apache License Version 2.0 (http://www.apache.org/licenses/)
Font Awesome
SIL OFL 1.1 (http://scripts.sil.org/OFL)
MIT License (http://opensource.org/licenses/mit-license.html)
CC BY 3.0 ( http://creativecommons.org/licenses/by/3.0/)
Powered by Worktribe © 2025
Advanced Search