Syntheses of 11-hydroxylated guaianolides
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Syntheses of 11-hydroxylated guaianolides. / Lauridsen, A.; Cornett, Claus; Vulpius, T.; Moldt, P.; Christensen, S. B.
In: Acta Chemica Scandinavica. Supplementum, Vol. 50, No. 2, 1996, p. 150-157.Research output: Contribution to journal › Journal article › Research › peer-review
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TY - JOUR
T1 - Syntheses of 11-hydroxylated guaianolides
AU - Lauridsen, A.
AU - Cornett, Claus
AU - Vulpius, T.
AU - Moldt, P.
AU - Christensen, S. B.
PY - 1996
Y1 - 1996
N2 - 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.
AB - 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.
KW - sesquiterpene lactones thapsigargin chemistry
M3 - Tidsskriftartikel
VL - 50
SP - 150
EP - 157
JO - Acta Chemica Scandinavica. Supplementum
JF - Acta Chemica Scandinavica. Supplementum
SN - 0065-1133
IS - 2
ER -
ID: 38061827