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α-Functionalisation of Cyclic Sulfides Enabled by Lithiation Trapping.
Seling, Nico; Atobe, Masakazu; Kasten, Kevin; Firth, James D; Karadakov, Peter B; Goldberg, Frederick W; O'Brien, Peter.
Afiliação
  • Seling N; Department of Chemistry, University of York, York, YO10 5DD, UK.
  • Atobe M; Department of Chemistry, University of York, York, YO10 5DD, UK.
  • Kasten K; Modulus Discovery, Inc., Daiichi Hibiya Building 7th Floor1-18-21 Shimbashi Minato-ku, Tokyo, 105-0004, Japan.
  • Firth JD; Department of Chemistry, University of York, York, YO10 5DD, UK.
  • Karadakov PB; Department of Chemistry, University of York, York, YO10 5DD, UK.
  • Goldberg FW; Department of Chemistry, University of York, York, YO10 5DD, UK.
  • O'Brien P; Oncology R&D, AstraZeneca, 1 Francis Crick Ave, Cambridge, CB2 0AA, UK.
Angew Chem Int Ed Engl ; 63(2): e202314423, 2024 Jan 08.
Article em En | MEDLINE | ID: mdl-37984884
ABSTRACT
A general and straightforward procedure for the lithiation trapping of cyclic sulfides such as tetrahydrothiophene, tetrahydrothiopyran and a thiomorpholine is described. Trapping with a wide range of electrophiles is demonstrated, leading to more than 50 diverse α-substituted saturated sulfur heterocycles. The methodology provides access to a range of α-substituted cyclic sulfides that are not easily synthesised by the currently available methods.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Reino Unido