183199-41-9Relevant academic research and scientific papers
An efficient preparation of peri-hydroxy dihydroquinone derivatives through a Pummerer-type rearrangement of silylene-protected peri-hydroxy aromatic sulfoxides
Kita, Yasuyuki,Takeda, Yoshifumi,Iio, Kiyosei,Yokogawa, Kayoko,Takahashi, Kenji,Akai, Shuji
, p. 7545 - 7548 (2007/10/03)
Silylene protection of two dihydroxy groups of the peri-hydroxy aromatic sulfides 6a-f was essential for the subsequent Pummerer-type reaction. The overall process provided a novel and efficient approach to the peri-hydroxy dihydroquinone derivatives 9a-f.
