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Inter- and intramolecular rearrangements of cyanuric acid triallyl esters

✍ Scribed by V. R. Likhterov; S. V. Klenovich; V. S. étlis; L. A. Tsareva; é. G. Pomerantseva; S. M. Shmuilovich

Publisher
Springer US
Year
1988
Tongue
English
Weight
333 KB
Volume
24
Category
Article
ISSN
0009-3122

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## Abstract Bicyclo[2.2.0]hex‐5‐ene‐2‐endo‐carboxylic acids and their methyl esters give the corresponding γ‐lactones, together with isomerized products, upon treatment with hydrochloric acid in acetic acid. The reaction mechanism is discussed.