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- W4386558049 abstract "Nitration of aromatic aldehydes with difluoromethoxy group results in the partial ipso-substitution of the aldehyde group if difluoromethoxy group is located in the para-position to the aldehyde group. The presence of a chlorine atom in the meta-position to the aldehyde group increases the contribution of the ipso-substitution, while the presence of a chlorine atom in the ortho-position to the aldehyde group reduces it. The presence of strong donors (alkoxy groups) in the molecule eliminates the contribution of the ipso-substitution." @default.
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- W4386558049 date "2023-09-05" @default.
- W4386558049 modified "2023-10-16" @default.
- W4386558049 title "Features of Nitration of Aromatic Aldehydes with the Difluoromethoxy Group" @default.
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- W4386558049 doi "https://doi.org/10.24959/ophcj.23.285469" @default.
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