Syntheses of 11-hydroxylated guaianolides

Research output: Contribution to journal › Journal article › Research › peer-review

Standard

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

Harvard

Lauridsen, A, Cornett, C, Vulpius, T, Moldt, P & Christensen, SB 1996, 'Syntheses of 11-hydroxylated guaianolides', Acta Chemica Scandinavica. Supplementum, vol. 50, no. 2, pp. 150-157.

APA

Lauridsen, A., Cornett, C., Vulpius, T., Moldt, P., & Christensen, S. B. (1996). Syntheses of 11-hydroxylated guaianolides. Acta Chemica Scandinavica. Supplementum, 50(2), 150-157.

Vancouver

Lauridsen A, Cornett C, Vulpius T, Moldt P, Christensen SB. Syntheses of 11-hydroxylated guaianolides. Acta Chemica Scandinavica. Supplementum. 1996;50(2):150-157.

Author

Lauridsen, A. ; Cornett, Claus ; Vulpius, T. ; Moldt, P. ; Christensen, S. B. / Syntheses of 11-hydroxylated guaianolides. In: Acta Chemica Scandinavica. Supplementum. 1996 ; Vol. 50, No. 2. pp. 150-157.

Bibtex

@article{23d0ea2d3dc6459582bbffb7a268cc3b,
title = "Syntheses of 11-hydroxylated guaianolides",
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.",
keywords = "sesquiterpene lactones thapsigargin chemistry",
author = "A. Lauridsen and Claus Cornett and T. Vulpius and P. Moldt and Christensen, {S. B.}",
year = "1996",
language = "Udefineret/Ukendt",
volume = "50",
pages = "150--157",
journal = "Acta Chemica Scandinavica. Supplementum",
issn = "0065-1133",
publisher = "Acta Chemica Scandinavica. Supplementum",
number = "2",

}

RIS

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