| Literature DB >> 31674791 |
Helen L Barlow1, Pauline T G Rabet1, Alastair Durie1, Tim Evans1, Michael F Greaney1.
Abstract
A range of electron-poor and heterocyclic sulfonamides react with phenylacetyl chlorides to produce benzhydryl derivatives in a single step. The reaction proceeds via tandem amide bond formation/Dohmori-Smiles rearrangement under the simple conditions of an aqueous base. In the case of o-nosylamides, a further reaction takes place at the nitro group to yield indazoles.Entities:
Year: 2019 PMID: 31674791 DOI: 10.1021/acs.orglett.9b03429
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005