Obtention de nouveaux squelettes diterpéniques lors de l'isomérisation d'époxydes diterpéniques sur alumine active
Keyword(s):
The isomerization of diterpene epoxides on active neutral alumina has established the existence of new rearrangements of the diterpene skeleton. Methyl 8,14β-epoxysandarcopimarate leads to bicyclic diterpene compounds by a Grob fragmentation, to derivatives of cleistanthane by a 1,2 migration of the vinyl substituent, as well as to one cycloditerpene compound. The 7,8 (or 8,9) derivatives of methyl isopimarate lead essentially to hydroxyolefins formed by a bifunctional acid–base mechanism at the alumina surface. [Journal translation]
2013 ◽
Vol 117
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pp. 12268-12279
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1987 ◽
Vol 45
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pp. 19-34
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1994 ◽
Vol 116
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pp. 11631-11635
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1948 ◽
Vol 41
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pp. 27
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2019 ◽
Vol 89
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pp. 255-260
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2007 ◽
Vol 33
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pp. 123-129