Chemistry Letters p. 1415 - 1418 (1988)
Update date:2022-09-26
Topics:
Kang, Wen-Bing
Nan'Ya, Seiko
Toru, Takeshi
Ueno, Yoshio
The regioselective addition of lithium enolates to thio-substituted 1,4-naphthoquinones gave alkylated 1,4-naphthoquinones via 1,4-addition products.A phenacyl 1,4-naphthoquinone was cyclized to a naphthofuran-4,9-dione ring system.
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