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- W2950223102 abstract "The first synthesis of spirolactone (+)-vitedoin B (14 steps, 8.0% global yield) and spiro enol ether (+)-negundoin A (19 steps, 3.7% global yield), via a nor-labdane acetoxy ester, has been achieved starting from commercial (+)-abietic acid." @default.
- W2950223102 created "2019-06-27" @default.
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- W2950223102 date "2014-04-24" @default.
- W2950223102 modified "2023-10-18" @default.
- W2950223102 title "Stereoselective Transformations of (+)-Abietic Acid into (+)-Vitedoin B and (+)-Negundoin A" @default.
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- W2950223102 doi "https://doi.org/10.1021/jo5003533" @default.
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