Synthesis of macrocycles with one and more ent-beyerane skeletons based on the diterpenoid isosteviol
Macrocycles with one and more ent -beyerane skeletons were prepared by the reaction of 16,19-dihydroxyent-beyerane with several dibasic carboxylic acid chlorides. The structures of the synthesized compounds, namely, the number of ent -beyerane skeletons in the macrocycle, depended on the length of t...
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Veröffentlicht in: | Chemistry of natural compounds 2011-07, Vol.47 (3), p.422-427 |
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Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | Macrocycles with one and more
ent
-beyerane skeletons were prepared by the reaction of 16,19-dihydroxyent-beyerane with several dibasic carboxylic acid chlorides. The structures of the synthesized compounds, namely, the number of
ent
-beyerane skeletons in the macrocycle, depended on the length of the polymethylene chain in the acid chloride. The molecular structures of two of the synthesized macrocycles were establishedby x-ray crystal structures. |
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ISSN: | 0009-3130 1573-8388 |
DOI: | 10.1007/s10600-011-9949-6 |