ARTICLE;
CHIRALITY;
CONTROLLED STUDY;
DRUG DETERMINATION;
DRUG ISOLATION;
DRUG STRUCTURE;
DRUG SYNTHESIS;
PHYTOCHEMISTRY;
PLANT ROOT;
PROTON NUCLEAR MAGNETIC RESONANCE;
STEVIA;
STEVIA TOMENTOSA;
CHEMICAL STRUCTURE;
CHEMISTRY;
PLANT;
Kinghorn AD (Eds.), Stevia: the genus Stevia; Ch. 5. Taylor & Francis, London
Cerda-García-Rojas CM, Pereda-Miranda R. (2002) The phytochemistry of Stevia: a general survey. In: Kinghorn AD (Eds.), Stevia: the genus Stevia; Medicinal and Aromatic Plants Industrial Profiles, Vol. 19, Ch. 5. Taylor & Francis, London, pp. 86-118.
DOI 10.1016/S0031-9422(99)00217-4, PII S0031942299002174
Sánchez-Arreola E, Cerda-García-Rojas CM, Román LU, Hernández JD, Joseph-Nathan P. (1999) Longipinene derivatives from Stevia porphyrea. Phytochemistry, 52, 473-477. (Pubitemid 29436351)
Absolute configuration of the α-methylbutyryl residue in longipinene derivatives from Stevia pilosa
DOI 10.1016/j.phytochem.2004.12.001, Reports on Structure Elucidation
Álvarez-García R, Torres-Valencia JM, Román LU, Hernández JD, Cerda-García-Rojas CM, Joseph-Nathan P. (2005) Absolute configuration of the α-methylbutyryl residue in longipinene derivatives from Stevia pilosa. Phytochemistry, 66, 639-642. (Pubitemid 40357952)
Kiem PV, Minh CV, Huong HT, Nam NH, Lee JJ, Kim YH. (2004) Pentacyclic triterpenoids from Mallotus apelta. Archives of Pharmacal Research, 27, 1109-1113.
Flavonoids from Distemonanthus benthamianus Baillon. Methoxylated flavones and inter-relationships of benthamianin, a [2]benzopyrano-[4,3-b][1] benzopyran
Malan E, Roux DG. (1979) Flavonoids from Distemonanthus benthamianus Baillon. Methoxylated flavones and inter-relationships of benthamianin, a [2]benzopyrano-[4,3-b][1]benzopyran. Journal of the Chemical Society, Perkin Transaction 1, 2696-2703.
Chemical composition and antioxidant activity of phenolic compounds from wild and cultivated Sclerocarya birrea (Anacardiaceae) leaves
Braca A, Politi M, Sanogo R, Sanou H, Moreli I, Pizza C, De Tommasi N. (2003) Chemical composition and antioxidant activity of phenolic compounds from wild and cultivated Sclerocarya birrea (Anacardiaceae) leaves. Journal of Agricultural and Food Chemistry, 51, 6689-6695.
The absolute configuration of a sesquiterpene enone from Stevia purpurea and a phenol from Lasianthaea podocephala
Ghisalberti EL, Jefferies PR, Stuart AD. (1979) The absolute configuration of a sesquiterpene enone from Stevia purpurea and a phenol from Lasianthaea podocephala. Australian Journal of Chemistry, 32, 1627-1630.
The relationship between proton-proton NMR coupling constants and substituent electronegativities - I: An empirical generalization of the Karplus equation
Haasnoot CAG, de Leeuw FAAM, Altona C. (1980) The relationship between proton-proton NMR coupling constants and substituent electronegativities - I: An empirical generalization of the Karplus equation. Tetrahedron, 36, 2783-2792.