189811-41-4Relevant articles and documents
Oxidative Intramolecular [4+2]Cycloaddition of o-[(ω-Phenylthioethynyl)acyl]phenols Followed by the Aromatic Pummerer-type Reaction: A Novel Preparation of the peri-Hydroxy Dihydroquinone Structure
Akai, Shuji,Iio, Kiyosei,Takeda, Yoshifumi,Ueno, Hiroshi,Kita, Yasuyuki
, p. 310 - 312 (1997)
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.