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Pd/BIPHEPHOS is an Efficient Catalyst for the Pd-Catalyzed S-Allylation of Thiols with High n-Selectivity.
Schlatzer, Thomas; Schröder, Hilmar; Trobe, Melanie; Lembacher-Fadum, Christian; Stangl, Simon; Schlögl, Christoph; Weber, Hansjörg; Breinbauer, Rolf.
Afiliação
  • Schlatzer T; Institute of Organic Chemistry Graz University of Technology Stremayrgasse 9 A-8010 Graz Austria.
  • Schröder H; Institute of Organic Chemistry Graz University of Technology Stremayrgasse 9 A-8010 Graz Austria.
  • Trobe M; Institute of Organic Chemistry Graz University of Technology Stremayrgasse 9 A-8010 Graz Austria.
  • Lembacher-Fadum C; Institute of Organic Chemistry Graz University of Technology Stremayrgasse 9 A-8010 Graz Austria.
  • Stangl S; Institute of Organic Chemistry Graz University of Technology Stremayrgasse 9 A-8010 Graz Austria.
  • Schlögl C; Institute of Organic Chemistry Graz University of Technology Stremayrgasse 9 A-8010 Graz Austria.
  • Weber H; Institute of Organic Chemistry Graz University of Technology Stremayrgasse 9 A-8010 Graz Austria.
  • Breinbauer R; Institute of Organic Chemistry Graz University of Technology Stremayrgasse 9 A-8010 Graz Austria.
Adv Synth Catal ; 362(2): 331-336, 2020 Jan 23.
Article em En | MEDLINE | ID: mdl-32063821
The Pd-catalyzed S-allylation of thiols with stable allylcarbonate and allylacetate reagents offers several advantages over established reactions for the formation of thioethers. We could demonstrate that Pd/BIPHEPHOS is a catalyst system which allows the transition metal-catalyzed S-allylation of thiols with excellent n-regioselectivity. Mechanistic studies showed that this reaction is reversible under the applied reaction conditions. The excellent functional group tolerance of this transformation was demonstrated with a broad variety of thiol nucleophiles (18 examples) and allyl substrates (9 examples), and could even be applied for the late-stage diversification of cephalosporins, which might find application in the synthesis of new antibiotics.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article