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A reagent for the convenient, solid-phase synthesis of N-terminal peptide hydroxylamines for chemoselective ligations.

ABSTRACT: A new N-sulfonyloxaziridine reagent for the conversion of N-terminal peptide amines to the corresponding hydroxylamines without overoxidation or erosion of stereochemistry is described. The products are N-terminal hydroxylamines, which are substrates for chemoselective amide-bond forming reactions with alpha-ketoacids. The success of this reagent arises from covalent precomplexation with the substrate via imine bond formation followed by an intramolecular oxygen-atom transfer to the amine. An unexpected stereochemical mismatch between the racemic reagent and the chiral peptide substrates was addressed by the preparation of an enantipure version of this reagent and provides further support for the proposed mechanism.

SUBMITTER: Fukuzumi T

PROVIDER: S-EPMC2677186 | biostudies-literature | 2009 Mar

REPOSITORIES: biostudies-literature

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A reagent for the convenient, solid-phase synthesis of N-terminal peptide hydroxylamines for chemoselective ligations.

Fukuzumi Takeo T Bode Jeffrey W JW

Journal of the American Chemical Society 20090301 11

A new N-sulfonyloxaziridine reagent for the conversion of N-terminal peptide amines to the corresponding hydroxylamines without overoxidation or erosion of stereochemistry is described. The products are N-terminal hydroxylamines, which are substrates for chemoselective amide-bond forming reactions with alpha-ketoacids. The success of this reagent arises from covalent precomplexation with the substrate via imine bond formation followed by an intramolecular oxygen-atom transfer to the amine. An un ...[more]

PMID: 19256487

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