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- W2090671036 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-α-amino acid proline derivatives." @default.
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- W2090671036 date "2008-08-13" @default.
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- W2090671036 title "Synthesis of Carbapyochelins via Diastereoselective Azidation of 5-(Ethoxycarbonyl)methylproline Derivatives" @default.
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- W2090671036 doi "https://doi.org/10.1021/jo801294p" @default.
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