Abstract
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.
Original language | Undefined/Unknown |
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Journal | Acta Chemica Scandinavica. Supplementum |
Volume | 50 |
Issue number | 2 |
Pages (from-to) | 150-157 |
Number of pages | 8 |
ISSN | 0065-1133 |
Publication status | Published - 1996 |