Abstract
Mass spectral data are
reported for eight 3-hydroxyflavanones, ten flavan-3-ols, and twelve flavan-3,4-diol derivatives. The principal
fragmentation of each of these three classes of compound yields ions derived by
retro Diels-Alder fission of the heterocyclic
nucleus, accompanied in the case of 3-hydroxyflavanones
and flavan-3-ols by hydrogen transfer from the
3-hydroxyl group to the A ring fragment. Deuteration
experiments with flavan-3-ols confirmed the origin of
the hydrogen atom transferred. Flavan-3,4-diols show two
characteristic fragmentation patterns depending on the insertion technique.
Mass spectra obtained by indirect insertion of flavan-3,4-diols showed a very
marked enhancement of the intensities of the M-18 and M-18-28 peaks, and of
their fragmentation ions, compared with spectra obtained by direct insertion.
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