Tetrahedron Letters p. 7529 - 7532 (1999)
Update date:2022-08-11
Topics:
Saito, Shinichi
Tsuboya, Norie
Chounan, Yukiyasu
Nogami, Tsutomu
Yamamoto, Yoshinori
We report the high reactivity of alkoxycarbonyl- and cyanoenynes in the homo-benzannulation of conjugated enynes. The introduction of these electron-withdrawing groups enabled us to carry out the benzannulation of 1-substituted enynes as well as 1,2- and
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