Nilsson, Kurt G. I. published the artcileA simple strategy for changing the regioselectivity of glycosidase-catalyzed formation of disaccharides. Part II. Enzymic synthesis in situ of various acceptor glycosides, Application In Synthesis of 2595-07-5, the main research area is galactopyranoside acceptor preparation; transglycosidation lactose galactosidase; raffinose transglycosidation; galactopyranosylgalactopyranoside disaccharide.
β-D-Galactosidase induced the formation of allyl, benzyl, and trimethylsilylethyl β-D-galactopyranosides on a 1-20 g scale from lactose and allyl alc., benzyl alc., and trimethylsilylethanol. Similarly, α-D-galactosidase catalyzed the formation of allyl α-D-galactopyranoside from raffinose and allyl alc. The galactosides were used as acceptors for the preparation of several galactopyranosylgalactopyranoside disaccharides.
Carbohydrate Research published new progress about Glycosides Role: SPN (Synthetic Preparation), PREP (Preparation). 2595-07-5 belongs to class alcohols-buliding-blocks, name is (2R,3R,4S,5R,6R)-2-(Allyloxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol, and the molecular formula is C9H16O6, Application In Synthesis of 2595-07-5.
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts