Home > News > Enantioselective amination of silylketene acetals with [N-(arylsufonyl)imino]phenyliodinanes catalyzed by chiral dirhodium(II)  carboxylatesa

Enantioselective amination of silylketene acetals with [N-(arylsufonyl)imino]phenyliodinanes catalyzed by chiral dirhodium(II)  carboxylatesa

June 20, 2024

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    Enantioselective amination of silylketene acetals with [N-(arylsufonyl)imino]phenyliodinanes catalyzed by chiral dirhodium(II)  carboxylatesa

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    Enantioselective amination of silylketene acetals with (N-arylsulfonylimino)phenyliodinanes catalyzed by chiral dirhodium(II) carboxylates: asymmetric synthesis of phenylglycine derivatives

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    Table 1

  • Associated context:

    The reaction in CH2Cl2 proceeded smoothly at 0 ℃ to completion in less than 15 min, giving N-(2-nitrophenylsulfonyl)phenylglycine methyl ester (4b)21 in 95% yield after column chromatography on silica gel (Table 1, entry 1).

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