Bulletin of the Chemical Society of Japan p. 3853 - 3854 (1983)
Update date:2022-08-04
Topics:
Shimizu, Nobujiro
Yamaoka, Shintaro
Tsuno, Yuho
A series of five different 2,2-diphenyl-3-oxetanols was synthesized by photocycloadditiion of benzophenone and enol trimethylsilyl ethers followed by protolysis of the resultant 3-trimethylsiloxyoxetanes.Thermal cleavage and acid-catalyzed rearrangement of these oxetanes are described.
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