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- W2952350633 abstract "The diastereoselective imino 1,2-Wittig rearrangement of hydroximates provides a novel method for the construction of optically active α-hydroxy oxime ethers. Upon treatment with LDA, allyl p-methoxyphenylhydroximate carrying a chiral auxiliary smoothly underwent diastereoselective rearrangement to give the (R)-α-hydroxy oxime ether which was effectively converted into (+)-cytoxazone." @default.
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- W2952350633 date "2005-06-01" @default.
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- W2952350633 title "Preparation of optically active α-hydroxy oxime ether by diastereoselective imino 1,2-Wittig rearrangement of hydroximates and its application to synthesis of (+)-cytoxazone" @default.
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- W2952350633 doi "https://doi.org/10.1016/j.tetlet.2005.04.026" @default.
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