作者:Ramachandra V. Joshi、Virupax V. Badiger
DOI:10.1002/jhet.5570250107
日期:1988.1
dl-threo-2-Dichloroacetamidol-1-[3-(6-bromocoumarinyl)]propane-1,3-diol (7) was synthesized according to Sorm's method. The fragmentation of dichloroacetamidomethyl 3-(6-bromocoumarinyl)ketone (4) under electron impact is reported. The results of in vitro antibacterial screening of the newly synthesized compounds have been presented.
根据Sorm法合成了dl-苏--2--2-二氯乙酰胺-1- [3-(6-溴香豆基)]丙烷-1,3-二醇(7)。报道了在电子冲击下二氯乙酰氨基甲基3-(6-溴香豆基)酮(4)的断裂。已经提出了对新合成的化合物进行体外抗菌筛选的结果。