Abstract
Abstract By treatment with BF 3 -etheratelethylene glycol, cyclohexanone with a carbonyl function at the 2′-(or 3′-) position of γ-side chain underwent novel ring transformation to afford five- (or six-) membered rings, and the fused bicyclic rings (bicyclo[3.3.0]octanone skeleton) were readily converted to bridged bicyclic rings (bicyclo[3.2.1]octene derivative).
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