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- W2076876216 abstract "A strategy for achieving enantiodivergency from R-(−)-carvone in the context of synthesis of eudesmanes and dihydroagarofurans is disclosed, which involves, among other things, sequential setting of the C10 quaternary centre and recreation of the desired C7 isopropyl stereochemistry to enter the antipodal series. A synthesis of 1-deacetoxy-ent-orbiculin has been achieved as a demonstration of the effectiveness and applicability of this approach." @default.
- W2076876216 created "2016-06-24" @default.
- W2076876216 creator A5024849259 @default.
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- W2076876216 date "2015-03-01" @default.
- W2076876216 modified "2023-10-18" @default.
- W2076876216 title "An enantiodivergent protocol from R-(−)-carvone: synthesis of dihydroagarofuran sesquiterpenoid 1-deacetoxy-ent-orbiculin A" @default.
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- W2076876216 doi "https://doi.org/10.1016/j.tet.2015.01.033" @default.
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