With benzophenone (1a) and fluorenone (1b) anthracene hydride (AH−) rapidly forms the anions 3a, b of the corresponding tertiary alcohols 4a, b, the intense colour of the reaction mixture indicating the presence of the ketyls 2a, b. Excess of AH− converts 3a, b into the diarylcarbinols. a mechanism is proposed for this ketone reduction.
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Sommer et al. (1988) studied this question.
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