Inside Cover: Iterative Synthesis of 2‐Deoxyoligosaccharides Enabled by Stereoselective Visible‐Light‐Promoted Glycosylation (Angew. Chem. Int. Ed. 20/2022).

2-Deoxyglycosides, Bromine Radical, Intermolecular Hydroetherification, Photoreaction, Stereoselectivity The rapid constructions of oligosaccharides, 20-mer deoxyglycan, and digoxin are facilitated by a bromide-based hydrogen species through an electron transfer process. Keywords: 2-Deoxyglycosides; Bromine Radical; Intermolecular Hydroetherification; Photoreaction; Stereoselectivity EN 2-Deoxyglycosides Bromine Radical Intermolecular Hydroetherification Photoreaction Stereoselectivity 1 1 1 05/05/22 20220509 NES 220509 B A visible-light-promoted b iterative synthesis of 2-deoxyoligosaccharides is reported by De-Cai Xiong, Xin-Shan Ye, and co-workers in their Research Article (e202114726). [Extracted from the article]