Issue 15, 1992

Electrophile-induced intramolecular cyclization of ortho-(aryloxy)phenylalkynes to dibenz[b,f] oxepines

Abstract

Reaction of o-(aryloxy)phenylalkynes with electrophiles such as perchloric acid, tetrafluoroboric acid, benzenesulfenyl chloride, and iodine monochloride yielded dibenz[b,f]oxepine derivatives. Cyclization to the dibenz[b,f]oxepines competed with 1,2-addition of the electrophiles. The effect of substituents on the alkyne is also discussed.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1992, 1969-1973

Electrophile-induced intramolecular cyclization of ortho-(aryloxy)phenylalkynes to dibenz[b,f] oxepines

T. Kitamura, T. Takachi, H. Kawasato and H. Taniguchi, J. Chem. Soc., Perkin Trans. 1, 1992, 1969 DOI: 10.1039/P19920001969

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