Synthesis of the Macrolactone Cores of Maltepolides via a Diene–Ene Ring-Closing Metathesis Strategy
Keyword(s):
Synthesis of the C19-truncated maltepolide E has been accomplished via a diene–ene RCM strategy without damage to the C11–C14 alkenyl epoxy unit. Upon release of the C17-OH group, it attacked at the C14 position with double bond migration and epoxide ring-opening to furnish the C19-truncated maltepolide A and B as proposed for the biosynthesis of maltepolides. Preliminary cytotoxicity data of the synthesized C19-truncated maltepolides against L929 mouse fibroblast cell line suggest irrelevance of the vinyl epoxide and importance of the conjugated dienyl keto unit for the observed anticancer activity.
2018 ◽
Vol 296
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pp. 98-104
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2016 ◽
Vol 243
(7)
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pp. 1137-1148
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1987 ◽
Vol 52
(6)
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pp. 871-882
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2003 ◽
Vol 197
(1)
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pp. 103-109
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2020 ◽
Vol 4
(1)
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pp. 34-41
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