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- W2073713546 abstract "Electron transfer from α- (1) or β-pinene (2), to 2,3,5,6-tetrachlorobenzoquinone generates radical cations, which are rapidly deprotonated by the semiquinone radical anion. (1S,5S)-2 is converted to (1S,5S)-1 and (1R,5R)-1 yields a dehydrogenation product, verbenene, (1R,5R)-9 with essentially quantitative retention of optical activity. The results support chiral, “ring-closed” radical cation structures in which the allylic-quaternary cyclobutane CC bond retains a significant degree of bonding." @default.
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- W2073713546 date "1996-04-01" @default.
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- W2073713546 title "Electron transfer induced deprotonation of α- and β-pinene: Evidence for ring-closed vinylcyclobutane radical cations" @default.
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- W2073713546 doi "https://doi.org/10.1016/0040-4039(96)00332-2" @default.
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