Unusual stereoselectivity in sialic acid aldolase-catalyzed aldol condensations: Synthesis of both enantiomers of high-carbon monosaccharides
An inversion of stereoselectivity in aldol condensations catalyzed by sialic acid aldolase (from Escherichia coli, Shinko American Inc.) was observed when L-mannose, 6-deoxy-L-mannose, L-talose, 2-deoxy-L-glucose, 2-deoxy-L-rhamnose, N-acetyl-L-mannosamin
Studies on sialic acids. XXV. Synthesis of the α- and β-N-glycosides of 3-deoxy-D-glycero-D-galacto-2-nonulosonic acid (KDN)
Several α- and β-N-glycosides of 3-deoxy-D-glycero-D-galacto-2-nonulosonic acid (1, KDN) were synthesized under Vorbruggen and Williamson reaction conditions. Two hexa-O-acetyl derivatives of 1 were treated with trimethylsilyl derivatives of pyrimidine, 5
Nakamura,Furuhata,Yamasaki,Ogura
p. 3140 - 3144
(2007/10/02)
More Articles about upstream products of 145295-41-6