145295-41-6Relevant articles and documents
Unusual stereoselectivity in sialic acid aldolase-catalyzed aldol condensations: Synthesis of both enantiomers of high-carbon monosaccharides
Lin, Chun-Hung,Sugai, Takeshi,Halcomb, Randall L.,Ichikawa, Yoshitaka,Wong, Chi-Huey
, p. 10138 - 10145 (1992)
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
