92617-59-9Relevant articles and documents
A MODEL FOR OLEFIN HYDRATION: INTRAMOLECULAR NUCLEOPHILIC ADDITION OF PHENOLATE OXYGEN TO THE UNACTIVATED DOUBLE BOND
Evans, Christopher M.,Kirby, Anthony J.
, p. 1259 - 1268 (2007/10/02)
Two series of phenol-olefins with strained ground states cyclise rapidly to ethers at high pH, where the phenol is fully ionised.The reaction involves intramolecular nucleophilic addition of phenolate oxygen to a monoalkylethylene.A primary carbanion is n