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Copper-Catalyzed Borylative Couplings with C-N Electrophiles.
Talbot, Fabien J T; Dherbassy, Quentin; Manna, Srimanta; Shi, Chunling; Zhang, Shibo; Howell, Gareth P; Perry, Gregory J P; Procter, David J.
Afiliación
  • Talbot FJT; Department of Chemistry, University of Manchester, Oxford Road, Manchester, M13 9PL, UK.
  • Dherbassy Q; Department of Chemistry, University of Manchester, Oxford Road, Manchester, M13 9PL, UK.
  • Manna S; Department of Chemistry, University of Manchester, Oxford Road, Manchester, M13 9PL, UK.
  • Shi C; Department of Chemistry, University of Manchester, Oxford Road, Manchester, M13 9PL, UK.
  • Zhang S; School of Material and Chemical Engineering, Xuzhou University of Technology, Xuzhou, 221018, P. R. China.
  • Howell GP; Department of Chemistry, University of Manchester, Oxford Road, Manchester, M13 9PL, UK.
  • Perry GJP; Chemical Development Pharmaceutical Technology & Development, Operations, AstraZeneca, Macclesfield, UK.
  • Procter DJ; Department of Chemistry, University of Manchester, Oxford Road, Manchester, M13 9PL, UK.
Angew Chem Int Ed Engl ; 59(46): 20278-20289, 2020 11 09.
Article en En | MEDLINE | ID: mdl-32544295
Copper-catalyzed borylative multicomponent reactions (MCRs) involving olefins and C-N electrophiles are a powerful tool to rapidly build up molecular complexity. The products from these reactions contain multiple functionalities, such as amino, cyano and boronate groups, that are ubiquitous in medicinal and process chemistry programs. Copper-catalyzed MCRs are particularly attractive because they use a relatively abundant and non-toxic catalyst to selectively deliver high-value products from simple feedstocks such as olefins. In this Minireview, we explore this rapidly emerging field and survey the borylative union of allenes, dienes, styrenes and other olefins, with imines, nitriles and related C-N electrophiles.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Año: 2020 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Año: 2020 Tipo del documento: Article