Add time:08/22/2019         Source:sciencedirect.com

A thermally induced intramolecular 1,3-dipolar cycloaddition of an azidoester and subsequent sodium cyanoborohydride reduction of the resulting bicyclic vinylogous urethane to give a bicyclic aminolactone allows access to an eight carbon homologue of α-homomannojirimycin which is a weak fucosidase inhibitor. Intermediates with both an α- and β-amino acid moiety are described and may be useful for incorporation of homopipecolic acids into novel peptide libraries.

We also recommend Trading Suppliers and Manufacturers of homomannojirimycin (cas 127995-29-3). Pls Click Website Link as below: cas 127995-29-3 suppliers