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- W2051929406 abstract "The feasibilities of both the LDA-induced and silyl triflate-mediated [2,3]-sigmatropic rearrangements of α-allylamino esters were studied. While the former enolate rearrangement does not proceed under the usual [2,3]Wittig conditions, the latter rearrangement is shown to proceed via the N-silylated ylide to provide the formal amino-[2,3]Wittig product with a high diastereoselectivity." @default.
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- W2051929406 date "2010-08-22" @default.
- W2051929406 modified "2023-09-26" @default.
- W2051929406 title "ChemInform Abstract: Feasibility Studies on Amino-(2,3)Wittig Rearrangement. Silyl Triflate- Mediated(2,3)-Sigmatropic Rearrangement of α-Allylamino Esters." @default.
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- W2051929406 doi "https://doi.org/10.1002/chin.199211077" @default.
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