(+)-neo-olivil from roots of Urtica dioica

Phytochemistry
1997.0

Abstract

The all-trans configuration of (+)-neo-olivil from Urtica dioica was established by NMR-spectroscopy. After transforming it to (-)-epipinoresinol and (-)-pinoresinol with trimethylorthoformate and H2SO4 the absolute configuration was determined as 7R,7'R,8S,8'S. © 1997 Elsevier Science Ltd

Knowledge Graph

Similar Paper

(+)-neo-olivil from roots of Urtica dioica
Phytochemistry 1997.0
The Absolute Configuration of 1-(3‘,4‘-Dihydroxycinnamoyl)cyclopentane-2,3-diol from the Amazonian Tree <i>Chimarrhis </i><i>t</i><i>urbinata</i>
Journal of Natural Products 2006.0
Stereochemistry of the 4-hydroxyisoleucine from Trigonella foenum-graecum
Phytochemistry 1989.0
Uraline, a New Norditerpenoid Alkaloid from Aerial Parts of Delphinium uralense Nevski
Russian Journal of Bioorganic Chemistry 2005.0
New Chemical Constituents of<i>Euphorbia</i><i>q</i><i>uinquecostata</i>and Absolute Configuration Assignment by a Convenient Mosher Ester Procedure Carried Out in NMR Tubes
Journal of Natural Products 2002.0
Prenylcoumarins from Murraya paniculata var. omphalocarpa(Rutaceae): The Absolute Configuration of Sibiricin, Mexoticin and Omphamurin.
Chemical and Pharmaceutical Bulletin 1996.0
The absolute configuration of regelidine, a novel 6-nicotinoyl dihydroagarofuran sesquiterpene alkaloid from Tripterygium regelii.
Chemical and Pharmaceutical Bulletin 1987.0
Lignans from the Roots of<i>Urtica dioica</i>and their Metabolites Bind to Human Sex Hormone Binding Globulin (SHBG)
Planta Medica 1997.0
5′-O-demethyl-8-O-methyl-7-epi-dioncophylline a and its ‘regularly’ configurated atropisomer from Triphyophyllum peltatum
Phytochemistry 1994.0
The absolute configuration of regelidine, a novel 6-nicotinoyl dihydroagarofuran sesquiterpene alkaloid from Tripterygium regelii.
Chemical and Pharmaceutical Bulletin 1987.0