ARTICLE;
CARBON NUCLEAR MAGNETIC RESONANCE;
DRUG IDENTIFICATION;
DRUG ISOLATION;
DRUG STRUCTURE;
INFRARED SPECTROSCOPY;
LAPPULA ANOCARPA;
MASS SPECTROMETRY;
MEDICINAL PLANT;
NONHUMAN;
NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY;
PROTON NUCLEAR MAGNETIC RESONANCE;
STRUCTURE ANALYSIS;
4,5-Dihydroblumenol A, a new nor-isoprenoid from Perrottetia multiflora
Gonzáles AG, Guillermo JA, Ravelo AG, Jimenez IA (1994) 4,5-Dihydroblumenol A, a new nor-isoprenoid from Perrottetia multiflora. J Nat Prod 57: 400-402.
Mior and trace sterols in marine invertebrates 26: Isolation and structure elucidation of nine new 5α, 8α-epidioxy sterols from four marine organisms
Gunatilaka AAL, Gopichand Y, Schmitz FI, Djerassi C (1981) Mior and trace sterols in marine invertebrates 26: isolation and structure elucidation of nine new 5α, 8α-epidioxy sterols from four marine organisms. J Org Chem 46: 3860-3866.
In vitro fibrinolytic phytosterols isolated from the roots of Spatholobus suberetus
Yoshiyasu F, Yoshinori N, Geng PW, Wang R, Junko S, Bao XJ, Kazuyuki N (1988) In vitro fibrinolytic phytosterols isolated from the roots of Spatholobus suberetus. Planta Med 54: 34-36.
Axial selectivity of 1,2-nucleophilic addition to 2-(alkylidene) cyclohexanones: Is it higher than that of 2-cyclohexenone
You ZQ, Masato K (1993) Axial selectivity of 1,2-nucleophilic addition to 2-(alkylidene)cyclohexanones: is it higher than that of 2-cyclohexenone. Tetrahedron Lett 34: 2745-2748.