Tetrahedron Letters, volume 26, issue 7, pages 913-916

Biomimetic transformation of dehydrocurdione into curcumenol and isocurcumenol and their stereochemistries

YOSHINORI SHIOBARA ¹

Tomoko Iwata ¹

Mitsuaki Kodama ¹

Yoshinori Asakawa ¹

Tsunematsu Takemoto ¹

Yoshimasa Fukazawa ^{2, 3}

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Faculty of Pharmaceutical Sciences, Tokushima-bunri University, Tokushima 770, Japan |

Department of Chemistry, Hiroshima University, Hiroshima 730, JAPAN |

Faculty of Pharmaceutical Sciences, Tokushima Bunri University, Tokushima 770, Japan |

Publication type: Journal Article

Publication date: 1985-01-01

Elsevier

Journal: Tetrahedron Letters

scimago Q3

wos Q3

SJR: 0.323

CiteScore: 3.5

Impact factor: 1.5

ISSN: 00404039, 18733581

DOI: 10.1016/s0040-4039(00)61963-9

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Organic Chemistry

Drug Discovery

Biochemistry

Abstract

Dehydrocurdione, a sesquiterpene isolated from Curcuma zedoaria , was converted to curcumenol, isocurcumenol or new spirolactones in a highly selective manner and their absolute configurations were determined.

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Publisher

Elsevier

Journal

Tetrahedron Letters

scimago Q3

wos Q3

SJR

0.323

CiteScore

3.5

Impact factor

1.5

ISSN

00404039 (Print)

18733581 (Electronic)

Biomimetic transformation of dehydrocurdione into curcumenol and isocurcumenol and their stereochemistries

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