Regioselective Diversification of a Cardiac Glycoside, Lanatoside C, by Organocatalysis
Acylation of lanatoside C in the presence of organocatalyst 5 gave the C(4′′′′)-O-acylate in up to 90% regioselectivity (catalyst-controlled regioselectivity). Various functionalized acyl groups can be introduced at the C(4′′′′)-OH by a mixed anhydride method in the presence of 5 or the related orga...
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Veröffentlicht in: | Journal of organic chemistry 2012-09, Vol.77 (18), p.7850-7857 |
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Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Acylation of lanatoside C in the presence of organocatalyst 5 gave the C(4′′′′)-O-acylate in up to 90% regioselectivity (catalyst-controlled regioselectivity). Various functionalized acyl groups can be introduced at the C(4′′′′)-OH by a mixed anhydride method in the presence of 5 or the related organocatalyst. On the other hand, DMAP-catalyzed acylation of lanatoside C gave the C(3′′′′)-O-acylate in up to 97% regioselectivity (substrate-controlled regioselectivity). Thus, diverse regioselective introduction of acyl groups among eight free hydroxy groups of lanatoside C was achieved. |
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ISSN: | 0022-3263 1520-6904 |
DOI: | 10.1021/jo301007x |