1,6-Conjugate addition of zinc alkyls to para-quinone methides in a continuous-flow microreactor†

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Royal Society of Chemistry

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An efficient method for the synthesis of alkyl diarylmethanes through the 1,6-conjugate addition of dialkylzinc reagents to para-quinone methides (p-QMs) has been developed under continuous flow conditions using a microreactor. This protocol allows to access unsymmetrical alkyl diarylmethanes in moderate to excellent yields using a wide range of p-QMs and dialkylzinc reagents. Interestingly, this transformation worked well without the requirement of a catalyst.

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Organic and Biomolecular Chemistry, 15(1), pp. 56-60.

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