Syntheses of 11-hydroxylated guaianolides
Research output: Contribution to journal › Journal article › peer-review
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.
|Journal||Acta Chemica Scandinavica. Supplementum|
|Number of pages||8|
|Publication status||Published - 1996|