Thallium(III) p-tosylate (TTS) mediated oxidative rearrangement of 2-naphthyl and 2-heteroarylchromanones
Abstract
A practical and effective approach towards the synthesis of 3-hetroaryl-4H-chromen-4-ones by the oxidative rearrangement of the respective 2-hetroaryl chroman-4-ones using thallium(III) p-tosylate is described. The oxidative rearrangement of α and β-naphthyl and thiophene behave like aryl groups. However, pyridyl groups give only the dehydrogenated product.
Keyword(s)
Oxidative rearrangements, thallium(III) p-tosylate, dehydrogenation, thallium(III) acetate, 2- and 3-(β-naphthyl) chromones, 2- and 3-(2-theinyl)chromones, 2- and 3-(3-theinyl)chromones, 2-(3-pyridyl)chromones, 2-(4-pyridyl)chromones
Full Text: PDF (downloaded 555 times) PDF (downloaded 555 times)
Refbacks
- There are currently no refbacks.