A facile tetrahydrothiophene-catalyzed ylide route to vinyloxiranes.
Kai Li, Xianming Deng, Yong Tang
Abstract
Kai Li, Xianming Deng, Yong Tang
Abstract
Access to vinyloxiranes using aldehydes and allylic bromides in the presence of 1-5 mol% tetrahydrothiophene is reported. Both aliphatic and aromatic aldehydes work well in this reaction and the catalyst loading could be reduced as low as 0.5 mol%.
OpenAlex reports 19 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Access to vinyloxiranes using aldehydes and allylic bromides in the presence of 1-5 mol% tetrahydrothiophene is reported. Both aliphatic and aromatic aldehydes work well in this reaction and the catalyst loading could be reduced as low as 0.5 mol%.
Key concepts: Tetrahydrothiophene, Catalysis, Allylic rearrangement, Ylide, Chemistry, Organic chemistry, Medicinal chemistry