Abstract
AbstractAn efficient and simple IBX-promoted oxidative ring-opening of spiro-cyclopropanyl-cyclohexadienones was developed. Disubstituted para-quinone methides were obtained with good to excellent yields and high regioselectivity (33 examples, 45–90% yields). This convenient transformation provides a new method to construct significant para-quinone methides and features high efficiency, broad substrate scope, and good functional group compatibility
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