The Reaction of arylatrloxythiophosphoric hydrazide 2a～2d with glycosyl isothiocyanates 3a～3d gave the corresponding aryl N-（glycosylthioureylene）-arylthiophosphoramidates 4a～4d,5a～5d,6a～6d,7a～7d.The resulted ...The Reaction of arylatrloxythiophosphoric hydrazide 2a～2d with glycosyl isothiocyanates 3a～3d gave the corresponding aryl N-（glycosylthioureylene）-arylthiophosphoramidates 4a～4d,5a～5d,6a～6d,7a～7d.The resulted compounds contained glycosylthioureylene and thiophosphoric amide fragments.The glycosyl isothiocyanates 3a～3d were prepared by the reaction of α-D-glycosyl bromides with Pb（SCN）2.The biologic activities of the representative compounds were studied.展开更多
文摘The Reaction of arylatrloxythiophosphoric hydrazide 2a～2d with glycosyl isothiocyanates 3a～3d gave the corresponding aryl N-（glycosylthioureylene）-arylthiophosphoramidates 4a～4d,5a～5d,6a～6d,7a～7d.The resulted compounds contained glycosylthioureylene and thiophosphoric amide fragments.The glycosyl isothiocyanates 3a～3d were prepared by the reaction of α-D-glycosyl bromides with Pb（SCN）2.The biologic activities of the representative compounds were studied.
