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- W2079258085 abstract "A study of the nuclear magnetic resonance, infrared, and ultraviolet spectra showed that some doubly and triply ortho-substituted diphenyl ethers adopt, principally but not exclusively, the H-inside conformation, while the quadruply ortho-substituted 7-(4′-carbomethoxy-2′,6′-dinitrophenoxy)metameconine (V) adopts the methoxy-insideconformation. Interconversion of conformational isomers is extremely fast. Reduction of methyl 4-methoxy-3-nitrobenzoate with tin and hydrochloric acid gave methyl 3-amino-2-chloro-4-methoxybenzoate." @default.
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- W2079258085 date "1964-11-01" @default.
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- W2079258085 title "THE PRINCIPAL CONFORMATIONS OF SOME ORTHO-SUBSTITUTED DIPHENYL ETHERS" @default.
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- W2079258085 doi "https://doi.org/10.1139/v64-373" @default.
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