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- W2092033416 abstract "1H n.m.r. spectra of 36 derivatives of 6-acetoxy-2,4-cyclohexadienones were analysed. All available evidence indicates that all members of the series have similar conformations which do not depart significantly from planarity. Substituent-induced chemical shifts and interproton coupling constants correlate well with those in the analogously substituted ethylene and benzene derivatives. In particular, it appears that a substituent on the central carbon atom exerts a similar influence on 4J(HH) across a ‘W’ path when the three intervening carbon atoms are a part of a benzene ring, an allylic system (i.e. sp3–sp2–sp2), a localized sp2–sp2–sp2 system or a saturated (i.e. sp3–sp3–sp3) system." @default.
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- W2092033416 date "1977-03-01" @default.
- W2092033416 modified "2023-10-16" @default.
- W2092033416 title "1H n.m.r. spectra of 6-acetoxy-2,4-cyclohexadienones" @default.
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- W2092033416 doi "https://doi.org/10.1002/mrc.1270090314" @default.
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