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- W1974233152 abstract "The 1H-NMR spectra of a series of chlorinated norbornene and derived norbornanone and norbornane systems have been recorded and analysed. Several characteristics of the observed spectral parameters can be explained by considering the rotameric behaviour of the endo-CH2X group that shows a preference for a conformation with the C-X bond synclinal to the methine proton of the carbon it is attached to." @default.
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- W1974233152 date "2010-09-01" @default.
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- W1974233152 title "1H-NMR spectral study of chlorinated derivatives of the norbornane system. Rotameric Preference of an Endo CH2X Group." @default.
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- W1974233152 doi "https://doi.org/10.1002/bscb.19780870207" @default.
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