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.
Study of the reactivity of squarylferrocenes. Addition of amines and aminoesters
Et3B, an Efficient Mediator for Xanthate Transfer Based Radical Processes
Diastereoselective alkylation of chiral glycinate derivatives containing the ?-phenylethyl group.
Synthesis of new homochiral 2,3-dialkylpiperazines derived from (R)-(?)-phenylglycinol
X-ray crystallographic study of neutral boron chelates with ?-diketones and tropolone
Diastereoselective Synthesis of Spiro-?-lactams via Staudinger Reaction