Bulletin of the Chemical Society of Japan p. 2657 - 2662 (1995)
Update date:2022-08-28
Topics:
Matsui, Makoto
Yamamoto, Hisashi
The regioselective protonation of acyclic polyene was achieved, dependent on the choice of catalyst.The addition of myrcene to trimethylhydroquinone, using boron trifluoride-diethyl ether (1/1), predominantly gave a spiro structure.When (+)-10-camphorsulfonic acid was used as a catalyst, the major compound produced was chroman.
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