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The Thio-Claisen Rearrangement. The Mechanism of Thermal Rearrangement of Allyl Aryl Sulfides

โœ 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

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๐Ÿ“œ SIMILAR VOLUMES


The thio-Claisen rearrangement of allyl
โœ Yasuo Makisumi ๐Ÿ“‚ Article ๐Ÿ“… 1966 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 192 KB

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

The thio-Claisen rearrangements of allyl
โœ Yasuo Makisumi; Akira Murabayashi ๐Ÿ“‚ Article ๐Ÿ“… 1969 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 155 KB

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