Amat Tusón, MercedesFabregat, RobertGriera Farres, RosaBosch Cartes, Joan2017-03-102017-03-102009-02-200022-3263https://hdl.handle.net/2445/108263A practical synthetic route to enantiopure 5-substituted cisdecahydroquinolines has been developed, the key steps being a stereoselective cyclocondensation of 2-substituted 6-oxocyclohexenepropionates 2 with (R)-phenylglycinol, the stereoselective hydrogenation of the resulting unsaturated tricyclic lactams, and the stereoselective reductive cleavage of the oxazolidine ring.4 p.application/pdfeng(c) American Chemical Society , 2009QuinolonesSíntesi orgànicaLactamesReacció d'oxidació-reduccióQuinolone antibacterial agentsOrganic synthesisLactamsOxidation-reduction reactioninfo:eu-repo/semantics/article5660152017-03-10info:eu-repo/semantics/openAccess