2019-04-012019-04-0120131875-6271http://repositorio.colciencias.gov.co/handle/11146/34174An efficient preparation of the girgensohnine and its close analogs with α-aminonitrile structure, and their spectral characterization were reported for the first time. The piperidine α-aminonitriles were obtained through 5 mol% InCl3-catalyzed one-pot Strecker reaction and tested for antioxidant activity and AChE inhibitory properties. It was found that girgensohnine possesses a moderate AChE inhibitory property while its spiroanalog shows good antioxidant capacitypdf5 páginasenginfo:eu-repo/semantics/embargoedAccessFirst Girgensohnine Analogs Prepared Through InCl3-catalyzed Strecker Reaction and their BioprospectionArtículo científicoContiene 26 referencias bibliográficas. Véase documento adjuntoBiología vegetalProductos químicosAceites vegetalesAChE inhibitory activityAlkaloidsα-AminonitrilesAntioxidant capacityGirgensohnineStrecker reactionAceites esencialesBioquímica vegetalBiotecnologíaCatalizadores