Kinetics of Strain-Promoted Alkyne-Nitrone Cycloadditions (SPANC) with Unprotected Carbohydrate Scaffolded Nitrones
- 1 May 2024
- journal article
- research article
- Published by American Chemical Society (ACS) in Organic Letters
- Vol. 26 (18) , 3917-3922
Abstract
The use of unprotected carbohydrate-derived nitrones as partners in strain-promoted alkyne-nitrone cycloadditions was investigated as a new tool for bioconjugation. The observed second-order reactions displayed rate constants of 3.4 × 10-4-5.8 × 10-2 M-1 s-1, which is the common order of magnitude of reaction kinetics with other simple aliphatic or aromatic nitrones. Applicability of this method to aqueous media was demonstrated by performing a one-pot protocol, which combines sequential formation of the nitrone and cycloaddition with cyclooctyne in water.Keywords
Funding Information
- Centre National de la Recherche Scientifique
- Université de Reims Champagne-Ardenne
This publication has 40 references indexed in Scilit:
- Bioorthogonal chemistry: Bridging chemistry, biology, and medicineChem, 2023
- In Vivo Applications of Bioorthogonal Reactions: Chemistry and Targeting MechanismsChemistry – A European Journal, 2023
- To View Your Biomolecule, Click inside the CellAngewandte Chemie International Edition, 2021
- Cycloadditions of Trans‐Cyclooctenes and Nitrones as Tools for Bioorthogonal LabellingChemBioChem, 2019
- Getting a grip on glycans: A current overview of the metabolic oligosaccharide engineering toolboxCarbohydrate Research, 2016
- Strain-promoted cycloadditions involving nitrones and alkynes — rapid tunable reactions for bioorthogonal labelingCurrent Opinion in Chemical Biology, 2014
- Bioorthogonal Chemistry: Fishing for Selectivity in a Sea of FunctionalityAngewandte Chemie International Edition, 2009
- A Photoinducible 1,3‐Dipolar Cycloaddition Reaction for Rapid, Selective Modification of Tetrazole‐Containing ProteinsAngewandte Chemie International Edition, 2008
- Desoxy‐nitrozucker. 13. Mitteilung. Herstellung ungeschützter und partiell geschützter 1‐Desoxy‐1‐nitro‐D‐aldosen sowie Röntgenstrukturanalysen einiger ihrer VertreterHelvetica Chimica Acta, 1986
- Stereoselektivität und Reaktivität bei der 1,3‐dipolaren Cycloaddition chiraler N‐(Alkoxyalkyl)nitroneHelvetica Chimica Acta, 1977