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- W2024237189 endingPage "3974" @default.
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- W2024237189 abstract "In this, the second of two Letters, we describe an effective assembly of (+)-4, an eastern hemisphere subtarget comprising the FGH rings of (+)-nodulisporic acid A (1) (17 steps, 9% overall yield). Central to the synthesis is a Koga three-component conjugate addition-alkylation sequence which secures the trans orientation of the vicinal quaternary methyl groups. [reaction: see text]" @default.
- W2024237189 created "2016-06-24" @default.
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- W2024237189 date "2001-11-01" @default.
- W2024237189 modified "2023-10-03" @default.
- W2024237189 title "Nodulisporic Acid A Synthetic Studies. 2. Construction of an Eastern Hemisphere Subtarget" @default.
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- W2024237189 doi "https://doi.org/10.1021/ol016888t" @default.
- W2024237189 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/11720582" @default.
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