| [1] Webley D, Jones J D. Selevtive reaction of the free hydeoxyl groups of 2,3,4,3′,4′-penta-O-benzylsucrose[J]. J Carbohydr Chem，1996, 15:73-79.[2] Jones J D, Hacking A J, Cheetham P S. Biological Method for Protection of 6-position of Sucrose and Its Use in Synthesis of Disaccharide High Intensity Sweenter[J]. Biotechnol Bioeng, 1992, 39:203-210.[3] Rich J O, Bedell B A, Dordick J S. Controlling enzyme-catalysed regioselectivity in sugar ester synthesis[J]. Biotechnol Bioeng, 1995, 45:426-434.[4] Therisod M, Klibanov A M. Lipase-catalyzed irreversible transesterification using enol ester as reagents: preparative enantio- and regioselective synthsis of alcohol, glycerol derivatives, sugars and organometallies[J]. J Am Chem Soc, 1987, 109:3927-3932.[5] Riva S, Chopineau J, Kieboom A P G, et al. Protease catalyzed regioselective esterification of sugar and related compounds in anhydrous dimethylformamide[J]. J Am Chem Soc, 1988, 110:584-589.[6] Jones J B. Solvent variation inverts substrate specificity of a enzyme[J]. Tetrahedron, 1986, 42:3351-3357.[7] David S, Hanessian S. Regioselective manipulation of hydroxyl groups via organotin derivatives[J]. Tetrahedron, 1985, 41:643-663. |
