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• W2022267776 endingPage "1091" @default.
• W2022267776 startingPage "1088" @default.
• W2022267776 abstract "Nonproteinogenic amino acids are prepared by an unprecedented domino aza-Michael addition-1,3-dipolar cycloaddition, leading to enantiopure highly substituted pyrrolidinopyrazolines. Nonaflyl azide serves as highly effective diazo transfer reagent, forming the link between the conjugate addition and cycloaddition steps. The resulting pyrrolidinopyrazolines can be rapidly transformed to either α,β,γ-triamino acids or 3,4-methano-β-prolines. Peptide coupling can be regioselectively conducted at each of the amino groups." @default.
• W2022267776 created "2016-06-24" @default.
• W2022267776 creator A5014563631 @default.
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• W2022267776 date "2014-02-07" @default.
• W2022267776 modified "2023-10-03" @default.
• W2022267776 title "Asymmetric Domino Aza-Michael Addition/[3 + 2] Cycloaddition Reactions as a Versatile Approach to α,β,γ-Triamino Acid Derivatives" @default.
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• W2022267776 doi "https://doi.org/10.1021/ol403660w" @default.
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