Total Synthesis of Biselide A, A Cytotoxic Macrolide of Marine Origin
Abstract The total synthesis of biselide A based on our earlier strategy of synthesizing haterumalides is reported. The highlights of this approach are the use of regioselective enzymatic hydrolysis for the installation of a C20 oxygen functional group and an asymmetric aldol reaction for the stereo...
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Veröffentlicht in: | Synthesis (Stuttgart) 2017-07, Vol.49 (13), p.2958-2970 |
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Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | Abstract
The total synthesis of biselide A based on our earlier strategy of synthesizing haterumalides is reported. The highlights of this approach are the use of regioselective enzymatic hydrolysis for the installation of a C20 oxygen functional group and an asymmetric aldol reaction for the stereoselective introduction of a C3 oxygen functional group. |
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ISSN: | 0039-7881 1437-210X |
DOI: | 10.1055/s-0036-1588169 |