2026-10-21T12:45:57Zhttps://riubu.ubu.es/oai/request

oai:riubu.ubu.es:10259/39132025-04-22T10:06:25Zcom_10259_3593com_10259_5086com_10259_2604col_10259_3594

Guilarte Moreno, Verónica Castroviejo Fernández, Mª Pilar García García, Patricia Fernández Rodríguez, Manuel A. Sanz Díez, Roberto 2016-01-27T09:24:07Z 2016-01-27T09:24:07Z 2011-03 0022-3263 http://hdl.handle.net/10259/3913 10.1021/jo200406f 2,3-Dihaloanilines have been proved as useful starting materials for synthesizing 4-halo-1H-indoles. Subsequent or in situ functionalization of the prepared haloindoles allows the access to a wide variety of 2,4- or 2,3,4-regioselectively functionalized indoles in good overall yields. As no efficient synthetic routes to 2,3-dihaloanilines have been described in the literature, different approaches to the preparation of these 1,2,3-functionalized aromatic precursors are now presented. The most general one involves a Smiles rearrangement from the corresponding 2,3-dihalophenols and allows the preparation of 2,3-dihaloanilides in a straightforward and synthetically useful manner. eng info:eu-repo/semantics/openAccess Approaches to the synthesis of 2,3-dihaloanilines. Useful precursors of 4-functionalized-1 H-indoles info:eu-repo/semantics/article