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- W2952807947 abstract "Abstract Diethyl α-amino-α-alkyl-phosphonates are obtained in good to high enantiomeric excesses by alkylation of chiral phosphonoglycine equivalents embodying the camphor skeleton. The chelating effects in the alkylation step play an important role in enhancing the diastereoselectivity of the reaction as substantiated by semiempirical calculations (AM1)." @default.
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- W2952807947 date "2010-08-21" @default.
- W2952807947 modified "2023-09-26" @default.
- W2952807947 title "ChemInform Abstract: Asymmetric Synthesis of Diethyl α-Amino-α-alkyl- phosphonates by Alkylation of Chiral Phosphonoglycine Equivalents: Role of Chelating Effects." @default.
- W2952807947 cites W2041857201 @default.
- W2952807947 doi "https://doi.org/10.1002/chin.199301060" @default.
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