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Ni-Catalyzed Stereoconvergent Reductive Dimerization of Bromocyclobutenes.
Spieß, Philipp; Matheu, Sergio Armentia; Bauer, Adriano; Coussanes, Guilhem; Shaaban, Saad; Maulide, Nuno.
Affiliation
  • Spieß P; Institute of Organic Chemistry, University of Vienna, Währinger Straße 38, 1090 Vienna, Austria.
  • Matheu SA; Institute of Organic Chemistry, University of Vienna, Währinger Straße 38, 1090 Vienna, Austria.
  • Bauer A; Institute of Organic Chemistry, University of Vienna, Währinger Straße 38, 1090 Vienna, Austria.
  • Coussanes G; Institute of Organic Chemistry, University of Vienna, Währinger Straße 38, 1090 Vienna, Austria.
  • Shaaban S; Institute of Organic Chemistry, University of Vienna, Währinger Straße 38, 1090 Vienna, Austria.
  • Maulide N; Institute of Organic Chemistry, University of Vienna, Währinger Straße 38, 1090 Vienna, Austria.
Org Lett ; 26(1): 355-359, 2024 Jan 12.
Article de En | MEDLINE | ID: mdl-38147458
ABSTRACT
A nickel-catalyzed reductive dimerization of bromocyclobutenes to produce unusual and unprecedented cyclobutene dimers was developed. In a stereoconvergent procedure, various bromocyclobutenes were readily dimerized in good yields, with good diastereoselectivities and broad functional group tolerance. Notably, the presence of a carbonyl group in the starting material appears to dictate diastereoselectivity.

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: Org Lett Sujet du journal: BIOQUIMICA Année: 2024 Type de document: Article Pays d'affiliation: Autriche

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: Org Lett Sujet du journal: BIOQUIMICA Année: 2024 Type de document: Article Pays d'affiliation: Autriche