A simple strategy for changing the regioselectivity of glycosidase-catalysed formation of disaccharides: Part II, enzymic synthesis in situ of various acceptor glycosides
作者:Kurt G.I. Nilsson
DOI:10.1016/0008-6215(88)80063-6
日期:1988.9
trimethylsilylethanol, respectively. Similarly, α- d -galactosidase catalysed the formation of allyl α- d -galactopyranoside from raffinose and allyl alcohol. The galactosides were used as acceptors for the preparation of the following disaccharide glycosides: β- d -Gal-(1→3)-β- d -Gal-OCH2CHCH2, β- d -Gal-(1→6)-β- d -Gal-OCH2CHCH2, β- d -Gal-(1→3)-β- d -Gal-OBn, β- d -Gal-(1→6)-β- d -Gal-OBn, β- d -Gal-(1→3)-β-