172987-08-5Relevant articles and documents
Carbopeptoids: Peptides and diketopiperazines incorporating the anomeric centre of mannopyranose
Long, Daniel D.,Tennant-Eyles, Richard J.,Estevez, Juan C.,Wormald, Mark R.,Dwek, Raymond A.,Smith, Martin D.,Fleet, George W.J.
, p. 807 - 813 (2007/10/03)
An approach to the synthesis of D-mannopyranose derivatives incorporating an anomeric α-amino acid component is described. An N-acylated bicyclic [2.2.2] lactone, formed via an oxidative ring closure, provides access to a new class of glycopeptide analogues of D-mannopyranose and determines the anomeric configuration of compounds derived therefrom. The mannopyranose diketopiperazine may be equilibrated to the more stable furanose form under basic conditions; in general, mannopyranose derivatives containing an α-amino acid moiety at the anomeric position are less stable than the mannofuranose isomers.