Journal of the Chemical Society. Perkin transactions I p. 3221 - 3224 (1981)
Update date:2022-08-04
Topics:
Gilchrist, Thomas L.
Rees, Charles W.
Tuddenham, David
The trienones (1), (2), and (3) have been converted into the corresponding enolate anions by reaction with potassium hydride below -10 deg C.Methyl fluorosulphonate was added to each solution: with the trienones (1) and (3), transient 3aH-indenes (4a) and
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(1982)
