期刊
CHEMISTRYSELECT
卷 7, 期 44, 页码 -出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/slct.202202745
关键词
heterocyclization; iminodihydrofuran; Michael addition; nucleophilic substitution; thiazolidinone
The catalyst-free and eco-friendly synthesis of potentially bioactive compounds comprising iminodihydrofuran and thiazolidinone rings has been developed using two strategies from iminodihydrofuran thiosemicarbazones. The methodologies are simple, efficient, inexpensive, and yield good to excellent yields of the polyheteroconjugated products with operational simplicity.
We have developed the catalyst-free and eco-friendly synthesis of potentially bioactive compounds comprising iminodihydrofuran and thiazolidinone rings by subsequent Michael addition/ heterocyclization and nucleophilic substitution/heterocyclization reactions according to two strategies from iminodihydrofuran thiosemicarbazones. The methodologies are simple, efficient and inexpensive affording good to excellent yields of the polyheteroconjugated products with operational simplicity.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据