Literature DB >> 31674791

Arylation Using Sulfonamides: Phenylacetamide Synthesis through Tandem Acylation-Smiles Rearrangement.

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


  4 in total

1.  Modular synthesis of α-arylated carboxylic acids, esters and amides via photocatalyzed triple C-F bond cleavage of methyltrifluorides.

Authors:  Sifan Li; Paul W Davies; Wei Shu
Journal:  Chem Sci       Date:  2022-05-12       Impact factor: 9.969

2.  1,4-Aryl migration in ketene-derived enolates by a polar-radical-crossover cascade.

Authors:  Niklas Radhoff; Armido Studer
Journal:  Nat Commun       Date:  2022-06-02       Impact factor: 17.694

3.  Density Functional Theory Evaluation of a Photoinduced Intramolecular Aryl Ether Rearrangement.

Authors:  Péter Pál Fehér
Journal:  J Org Chem       Date:  2021-01-07       Impact factor: 4.354

4.  Diarylamine Synthesis via Desulfinylative Smiles Rearrangement.

Authors:  Thomas Sephton; Jonathan M Large; Sam Butterworth; Michael F Greaney
Journal:  Org Lett       Date:  2022-01-30       Impact factor: 6.005

  4 in total

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