Synlett p. 310 - 312 (1997)
Update date:2022-07-29
Topics:
Akai, Shuji
Iio, Kiyosei
Takeda, Yoshifumi
Ueno, Hiroshi
Kita, Yasuyuki
The combination of the oxidative intramolecular [4+2]cycloaddition of o-acylphenol derivatives 10a,b and 16 having the ω-phenylthioethynyl group in the acyl chain and the Pummerer-type reaction of the cyclization products afforded the peri-hydroxy dihydroquinones 9a,b and 18 in good overall yields.
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Doi:10.1055/s-1997-791
(1997)Doi:10.1021/ja00998a023
(1967)Doi:10.1016/S0957-4166(97)00096-7
(1997)Doi:10.1016/S0040-4039(97)00639-4
(1997)Doi:10.1016/S0960-894X(97)00164-9
(1997)Doi:10.1016/S0022-328X(96)06680-6
(1997)
