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Synthesis of Carbapyochelins via Diastereoselective Azidation of 5-(Ethoxycarbonyl)methylproline Derivatives

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-α-amino acid proline de...

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Detalhes bibliográficos
Main Authors: Liyanage, Wathsala, Weerasinghe, Laksiri, Strong, Roland K., Del Valle, Juan R.
Formato: Artigo
Idioma:Inglês
Publicado em: 2008
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2802343/
https://ncbi.nlm.nih.gov/pubmed/18698823
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/jo801294p
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