1999
Susana Rojas-Lima, Rosa L. Santillan Baca, Miguel-Angel Domínguez, Atilano Gutiérrez Furocoumarins of three species of the genus Dorstenia, Phytochemistry, 50, 863-868 (1999). DOI: http://dx.doi.org/10.1016/S0031-9422(98)00520-2
Abstract
Phytochemical studies of the roots of Dorstenia excentrica afforded a diastereoisomer of prandiol having the 2?S,1?S configuration, 4-[3-(4,5-dihydro-5,5-dimethyl-4-oxo-2-furanyl)-butoxy]-7H-furo[3,2-g][1]1benzopyran-7-one, psoralen and 7-hydroxycoumarin. The furocoumarins 5-[3-(4,5-dihydro-5,5-dimethyl-4-oxo-2-furanyl)-butoxyl]-7H-[3,2-[1]benzopyran-7-one and bergapten were also present in the roots of D. drakena, while 7-hydroxycoumarin, psoralen and the psoralen dimer were isolated from D. lindeniana. The structure of the psoralen dimer was established by X-ray diffraction analysis.
Diastereoselective alkylation of chiral glycinate derivatives containing the ?-phenylethyl group.
Synthesis and Structures of some Lithium and Sodium (Aminoalcoholato)hydrido Aluminates
Bis(acetylsalicylato-j2O,O00)diaquacadmium(II)
Diastereoselective Synthesis of Spiro-?-lactams via Staudinger Reaction
Structural studies of spiroarsoranes derived from 2-aminophenols