Synthesis of Carbapyochelins via Diastereoselective Azidation of 5-(Ethoxycarbonyl)methylproline Derivatives
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https://figshare.com/articles/dataset/Synthesis_of_Carbapyochelins_via_Diastereoselective_Azidation_of_5_Ethoxycarbonyl_methylproline_Derivatives/2912860
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资源简介：
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 derivatives.
创建时间：
2016-02-27
