๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Mechanism of the thio-claisen rearrangement of 3-methylallyl phenyl sulfide

โœ Scribed by T. A. Danilova; R. G. Aukharieva; S. N. Petrov; S. Ya. Grobovenko; E. A. Viktorova


Book ID
112348484
Publisher
Springer US
Year
1981
Tongue
English
Weight
278 KB
Volume
17
Category
Article
ISSN
0009-3122

No coin nor oath required. For personal study only.


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