92549-17-2Relevant academic research and scientific papers
Reversal of the regioselectivity in a cycloaddition of o-quinones by varying the position of alkoxy substituents
Kuboki, Atsuhito,Yamamoto, Toru,Taira, Mamie,Arishige, Tetsuya,Konishi, Rina,Hamabata, Mami,Shirahama, Mutsumi,Hiramatsu, Takeya,Kuyama, Kohei,Ohira, Susumu
, p. 2558 - 2561 (2008/09/21)
We have investigated the regioselective cycloaddition of o-quinones 1b-e with the protected sinapyl alcohol 2. It was found that the position of the alkoxy substituent on the o-quinone ring controlled the regioselectivity of the cycloaddition. In addition
