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Exopericyclic stereocontrol in Johnson–Claisen rearrangements of allylic sulfides

✍ Scribed by Craig, Donald; Harvey, John W.; O'Brien, Alexander G.; White, Andrew J. P.

Book ID
118273201
Publisher
Royal Society of Chemistry
Year
2010
Tongue
English
Weight
536 KB
Volume
46
Category
Article
ISSN
1359-7345

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The thio-Claisen rearrangement of allyl
The thio-Claisen rearrangement of allyl 4-quinolyl sulfides
✍ Yasuo Makisumi 📂 Article 📅 1966 🏛 Elsevier Science 🌐 French ⚖ 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