The Thio-Claisen Rearrangement. The Mechanism of Thermal Rearrangement of Allyl Aryl Sulfides
โ Scribed by Kwart, Harold; Evans, E. Robert
- Book ID
- 120364960
- Publisher
- American Chemical Society
- Year
- 1966
- Tongue
- English
- Weight
- 1011 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0022-3263
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
It was reported in our previous papers (1) that, on heating at 2oo0, ally1 bquinolyl ethers were readily converted into the Claisen products, 3-allyl-4(1H)quinolones, in good yields accompanying small amounts of ring closure products, P,%dihydrofuro-[ 32-cjquinolines. H A ? or HBr-AcOH Several previ
Earlier, we reported that the thio-Cloisen reorrongement of ally1 4quinolyl sulfides (I) to 2,3-dihydrothieno[3.2-clquinolines (III) proceeded through the prototropic cyclizotion of the initially formed 3-allyl-4(1 H)-quinolinethiones (II), on the basis of the quantitative transformation of II into