Bicyclic diazasugars 2. Synthesis and structures of L-arabinose and D-ribose analogues
暂无分享,去创建一个
[1] N. K. Dalley,et al. (7R,8S,9S,9aR)-Octahydro-7,8,9-trihydroxy- 2H-pyrido[1,2-a]pyrimidine: A Bicyclic Diazasugar , 1998 .
[2] G. Besra,et al. Inhibition of UDP-Gal Mutase and Mycobacterial Galactan Biosynthesis by Pyrrolidine Analogues of Galactofuranose , 1997 .
[3] Sophie Wilkinson,et al. Fuel chemistry focus of TWA Flight 800 investigation , 1997 .
[4] K. Tatsuta,et al. The Total Synthesis of a Glycosidase Inhibitor, Nagstatin , 1997 .
[5] A. Wadouachi,et al. A facile route to diastereomerically pure analogues of castanospermine and australine , 1996 .
[6] G. Jacob,et al. Glycosylation inhibitors in biology and medicine. , 1995, Current opinion in structural biology.
[7] J. Dennis,et al. Inhibitors of carbohydrate processing: A new class of anticancer agents. , 1995, Clinical Cancer Research.
[8] G. Kaushal,et al. Glycosidase inhibitors in study of glycoconjugates. , 1994, Methods in enzymology.
[9] D. Grierson,et al. Synthesis of (6R,7R,8S,8aR)-6,7,8-trihydroxyperhydro[1,3]thiazolo[3,2-a]pyridine and its 8aS-epimer. Novel, biologically active analogs of castanospermine , 1992 .
[10] T. Aoyagi,et al. The structure of nagstatin, a new inhibitor of N-acetyl-beta-D-glucosaminidase. , 1992, The Journal of antibiotics.
[11] A. Elbein. Glycosidase inhibitors: inhibitors of N‐linked oligosaccharide processing , 1991, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[12] S. Koda,et al. Structure of kifunensine, a new immunomodulator isolated from an actinomycete , 1989 .
[13] P. Dey. Further characterization of β-l-arabinosidase from Cajanus indicus , 1983 .
[14] P. Dey. β-l-arabinosidase from Cajanus inducus: A new enzyme , 1973 .