| Literature DB >> 21443246 |
Verónica Guilarte1, M Pilar Castroviejo, Patricia García-García, Manuel A Fernández-Rodríguez, Roberto Sanz.
Abstract
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.Entities:
Mesh:
Substances:
Year: 2011 PMID: 21443246 DOI: 10.1021/jo200406f
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354