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Asymmetric ?-amination of ?-keto esters using a guanidine-bisurea bifunctional organocatalyst.


ABSTRACT: An asymmetric ?-amination of ?-keto esters with azodicarboxylate in the presence of a guanidine-bisurea bifunctional organocatalyst was investigated. The ?-amination products were obtained in up to 99% yield with up to 94% ee.

SUBMITTER: Odagi M 

PROVIDER: S-EPMC4778535 | biostudies-other | 2016

REPOSITORIES: biostudies-other

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Asymmetric α-amination of β-keto esters using a guanidine-bisurea bifunctional organocatalyst.

Odagi Minami M   Yamamoto Yoshiharu Y   Nagasawa Kazuo K  

Beilstein journal of organic chemistry 20160204


An asymmetric α-amination of β-keto esters with azodicarboxylate in the presence of a guanidine-bisurea bifunctional organocatalyst was investigated. The α-amination products were obtained in up to 99% yield with up to 94% ee. ...[more]

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