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Asymmetric dearomatization of benzyl 1-naphthyl ethers via [1,3] O-to-C rearrangement.

Hongkun ZengGang WenLili LinXiaoming Feng
Published in: Chemical communications (Cambridge, England) (2024)
A catalytic asymmetric dearomatization reaction of benzyl 1-naphthyl ethers accelerated by a chiral N , N '-dioxide/Co(II) complex is disclosed. The reaction proceeds via an enantioselective [1,3] O-to-C rearrangement through a tight ion-pair pathway, providing a wide array of α-naphthalenone derivatives bearing an all-carbon quaternary center in high yields with excellent ee values.
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