Regio- and diastereoselective lipase-catalyzed preparation of acetylated 2-O-glucosylglycerols

• Published in: Tetrahedron: Asymmetry
• Main Authors: D. Colombo, F. Ronchetti, A. Scala, I. Taino, F. Albini, L. Toma
• Format: Article in Journal/Newspaper
• Language: English
• Published: 1994
• Subjects: Settore BIO/10 - Biochimica; Antarc*; Antarctica
• Online Access: http://hdl.handle.net/2434/176944; https://doi.org/10.1016/0957-4166(94)80181-9

2-O-(β-D-Glucopyranosyl)glycerol and 2-O-(2′,3′,4′,6′-tetra-O-acetyl-β-D-glucopyranosyl]glycerol have been submitted to lipase-catalyzed acetylation using Pseudomonas cepacia (LPS) and Candida antarctica (LCA) Upases in organic solvent. The reactions involved the glycerol moiety and were highly diastereoselective: LPS yielded the (2S)-1-O-acetylderivative, while, more interestingly, LCA yielded the (2R)-1-O-acetyl-derivative; in this way the natural compound lilioside A could be obtained. Conversely, lipase-catalyzed hydrolysis of the fully acetylated 1,3-di-O-acetyl-2-O-(2′,3′,4′,6′-tetra-O-acetyl-β-D-glucopyranosyl)glycerol using LCA fiunished the (2S)-1-O-acetyl-derivative showing the same steric preference as the reverse reaction.