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
Hauptverfasser: Ueda, Yoshihiro, Mishiro, Kenji, Yoshida, Keisuke, Furuta, Takumi, Kawabata, Takeo
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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.
ISSN:0022-3263
1520-6904
DOI:10.1021/jo301007x