Journal of the Chinese Chemical Society p. 391 - 400 (1998)
Update date:2022-08-11
Topics:
Wakabayashi, Hidetsugu
Kurihara, Teruo
Shindo, Kimio
Tsukada, Masaaki
Yang, Paw-Wang
Yasunami, Masafumi
Nozoe, Tetsuo
A very convenient, one-pot synthesis (over 80% yield) of 3-bromo-1,5- and -1,7-azulenequinones has been developed by bromination of azulene in aqueous tetrahydrofuran. Reduction of 3-bromo-1,5- and -1,7-azulenequinones with tin or zinc powder in acetic acid gave the parent 1,5- and 1,7-azulenequinones, and further reduction products.
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