Iron Porphyrin Catalysts Induce Stereospecific Glycosylation with Glycal Epoxides
Year: 2026
Type: article
Abstract: This account highlights an iron porphyrin-catalyzed highly stereospecific glycosylation method for glycal epoxides. This method is effective for a wide variety of previously challenging, hindered secondary sugar acceptors and a broad array of both electron-rich and electron-deficient glycal epoxide donors. It plays a pivot role in stereoselective heparan sulfate oligosaccharide synthesis, and the kinetic studies revealed that this glycosylation proceeds through SN2-type pathways with both primary and hindered secondary acceptors.
Source: Synlett
DOI: 10.1055/a-2861-7444
Institution: Brandeis University
Language: English
Subfield: Organic Chemistry
Field: Chemistry
Domain: Physical Sciences
Open Access status: green
OpenAlex ID: W7155188884
