Thiophenols as Protic Nucleophilic Triggers in Aryne Three-Component Coupling.


Journal

Organic letters
ISSN: 1523-7052
Titre abrégé: Org Lett
Pays: United States
ID NLM: 100890393

Informations de publication

Date de publication:
20 Nov 2020
Historique:
pubmed: 6 11 2020
medline: 6 11 2020
entrez: 5 11 2020
Statut: ppublish

Résumé

The synthetic potential of thiophenols as a protic nucleophilic trigger in the transition-metal-free and Grignard-reagent-free three-component coupling involving arynes is demonstrated. Employing aldehydes as the third component, the reaction allowed the mild and broad scope synthesis of 2-arylthio benzyl alcohol derivatives in good yields. Moreover, selenophenol could be used as the nucleophilic trigger, and activated ketones could be used as the third component in this reaction.

Identifiants

pubmed: 33151079
doi: 10.1021/acs.orglett.0c03494
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

9097-9101

Auteurs

Subrata Bhattacharjee (S)

Department of Organic Chemistry, Indian Institute of Science, Bangalore 560012, India.

Avishek Guin (A)

Department of Organic Chemistry, Indian Institute of Science, Bangalore 560012, India.

Rahul N Gaykar (RN)

Department of Organic Chemistry, Indian Institute of Science, Bangalore 560012, India.

Akkattu T Biju (AT)

Department of Organic Chemistry, Indian Institute of Science, Bangalore 560012, India.

Classifications MeSH