2026-06-17T16:48:22Zhttps://riubu.ubu.es/oai/request

oai:riubu.ubu.es:10259/42882021-11-10T09:38:24Zcom_10259_3593com_10259_5086com_10259_2604col_10259_3594

Suárez, Anisley Martínez Lara, Fernando Sanz Díez, Roberto 2016-12-01T10:00:54Z 2017-12-21T03:45:06Z 2016-12 1477-0520 http://hdl.handle.net/10259/4288 10.1039/c6ob02125e A new and efficient synthesis of α-functionalized α-indol-3-yl ketones from easily available indolyl α-acyloins is reported. This process, catalyzed by Brønsted or Lewis acids, involves an uncommon direct nucleophilic substitution reaction of a secondary α-carbonyl-substituted hydroxyl group. The described methodology allows the introduction of a variety of nucleophiles such as (hetero)arenes, thiophenols, nitroanilines and 1,3-dicarbonyl derivatives. The synthesized α-indol-3-yl carbonyl compounds are important synthetic targets also useful for accessing functionalized tryptophols and furan-3-yl indoles. eng info:eu-repo/semantics/openAccess Synthesis of α-functionalized α-indol-3-yl carbonyls through direct SN reactions of indol-3-yl α-acyloins info:eu-repo/semantics/article