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- W2762157071 abstract "Abstract Axial naphthols are applied in asymmetric halogenative dearomatization reactions under simple and mild conditions in the work presented herein. The axial‐to‐central chirality conversion is efficiently accomplished, and the desired halogenated dearomatization products are obtained in high yields and enantioselectivities. By using commercially available halogenation reagents, the asymmetric fluorinative, chlorinative and brominative dearomatization reactions of axial naphthols derived from BINOLs are achieved. (BINOL=1,1′‐Bi‐2‐naphthol) magnified image" @default.
- W2762157071 created "2017-10-20" @default.
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- W2762157071 date "2017-10-24" @default.
- W2762157071 modified "2023-10-16" @default.
- W2762157071 title "Asymmetric Dearomative Halogenation of β-Naphthols: The Axial Chirality Transfer Reaction" @default.
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- W2762157071 doi "https://doi.org/10.1002/adsc.201700745" @default.
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