Synthesis of carbapyochelins via diastereoselective azidation of 5-(ethoxycarbonyl)methylproline derivatives.

ABSTRACT: Two configurationally stable carbon-based analogues of pyochelin have been prepared from Boc-pyroglutamic acid-tert-butyl ester in 11 and 13 steps. Introduction of the amino group was achieved by a highly diastereoselective electrophilic azidation reaction to afford novel bis-alpha-amino acid proline derivatives.

SUBMITTER: Liyanage W 

PROVIDER: S-EPMC2802343 | biostudies-literature | 2008 Sep

REPOSITORIES: biostudies-literature