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Syntheses of 11-hydroxylated guaianolides

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Two epimeric guaianolides, both prepared from alpha-santonin, were 11-hydroxylated using 2-phenylsulfonyl-3-phenyloxaziridine as a reagent. Extensive use of protecting groups enabled selective acylation of the 3- and 10-hydroxy groups.
OriginalsprogUdefineret/Ukendt
TidsskriftActa Chemica Scandinavica. Supplementum
Vol/bind50
Udgave nummer2
Sider (fra-til)150-157
Antal sider8
ISSN0065-1133
StatusUdgivet - 1996

    Forskningsområder

  • sesquiterpene lactones thapsigargin chemistry

ID: 38061827