<p>Abstract. Previous studies on the Esenbeckia alata and Raputia heptaphylla,</p><p>both species belonging to the Rutaceae family, have shown</p><p>important results with respect to their chemistry. These species have</p><p>secondary metabolites (coumarins and alkaloids mainly), which act as</p><p>chemotaxonomic markers. This paper presents, for the first time, the phytochemical</p><p>work and isolated metabolites in these species: four coumarins:</p><p>bergapten, xanthyletin, xanthotoxin, 3-isoprenyl-4-methoxy-coumarin;</p><p>four alkaloids: skinmianine, kokusaginine, dictamnine, and 1-methyl-2-</p><p>methoxy-4-quinolone; two lignans: sesamin and mesodihydroguaiaretic</p><p>acid; two sterols: -sitosterol, stigmasterol; and a pentacyclic triterpene:</p><p>lupeol that have been isolated from leaves of E. alata. Five alkaloids</p><p>7-methoxy-2,2-dimethyl-2,6-dihidro-piran[3,2,c] quinolin-5-one, flindersiamine,</p><p>skinmianine, kokusaginine and dictamnine that have been isolated</p><p>from leaves of R. heptaphylla. Moreover, it presents a new method by</p><p>obtaining quinolone alkaloid analogue precursors trough the condensations</p><p>of Mannich adduct vinylogous and aldehydes followed by radical</p><p>cyclization to obtain products with high regio- and stereoselectivity.</p><p> </p>