
Chemistry Letters p. 135 - 138 (1981)
Update date:2022-08-02
Topics:
Tsuge, Otohiko
Ueno, Kazunori
Oe, Koji
The intramolecular anionic cyclization of o-cinnamyloxybenzylideneamines proceeded via an allyl anion and/or an azaallyl anion to give a mixture of 2,3-dihydrobenzofurans and/or a perhydropyrro<3,2-c>benzopyrane.In a similar reaction o-phenylpropargyloxyb
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