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Spectral data for bisgersolanolide (1) have been deposited as Supporting Information.
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0344681596
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20 skeletons. On structural grounds, the majority of these bis-diterpenes appear to be derived from a classical Diels-Alder reaction of a diterpenoid diene with an activated dienophile-containing diterpenoid precursor. For well-documented examples, see: (a) Falshaw, C. P.; King, T. J. J. Chem. Soc., Perkin Trans. 1 1983, 1749-1752.
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0042576519
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If either the diene or the dienophile is chiral and optically active, facially selective addition will give rise to a nonstatistical mixture of optically active diastereomers.
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18
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0001147462
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Cycloaddition reactions in organic synthesis
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Baldwin, J. E., Magnus, P. D., Eds.; Pergamon Press: London
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Carruthers, W.1
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