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- W2005065356 abstract "[structure: see text] Bifunctional macrolides projecting an anchor group to the right or left spatial position of the lactone ring were synthesized. The regioselectivity of the key [3 + 2] cycloaddition process was controlled by the remote cladinose group attached to the C-3 position. These conformationally constrained molecules were employed as molecular probes to study the ribosomal binding sites of bifunctional macrolide antibiotics." @default.
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- W2005065356 date "2002-02-21" @default.
- W2005065356 modified "2023-10-16" @default.
- W2005065356 title "Regioselective Synthesis of Bifunctional Macrolides for Probing Ribosomal Binding" @default.
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- W2005065356 doi "https://doi.org/10.1021/ol025554g" @default.
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