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Homo- and heterodehydrocoupling of phosphines mediated by alkali metal catalysts.
Wu, Lipeng; Annibale, Vincent T; Jiao, Haijun; Brookfield, Adam; Collison, David; Manners, Ian.
Afiliación
  • Wu L; School of Chemistry, University of Bristol, Cantock's Close, Bristol, BS8 1TS, UK.
  • Annibale VT; State Key Laboratory for Oxo Synthesis and Selective Oxidation, Suzhou Research Institute of Lanzhou Institute of Chemical Physics, CAS, 730000, Lanzhou, P. R. China.
  • Jiao H; School of Chemistry, University of Bristol, Cantock's Close, Bristol, BS8 1TS, UK.
  • Brookfield A; Leibniz-Institut für Katalyse e. V, Albert-Einstein-Straße 29a, 18059, Rostock, Germany.
  • Collison D; The School of Chemistry and the Photon Science Institute, The University of Manchester, Oxford Road, Manchester, M13 9PL, UK.
  • Manners I; The School of Chemistry and the Photon Science Institute, The University of Manchester, Oxford Road, Manchester, M13 9PL, UK.
Nat Commun ; 10(1): 2786, 2019 Jun 26.
Article en En | MEDLINE | ID: mdl-31243267
Catalytic chemistry that involves the activation and transformation of main group substrates is relatively undeveloped and current examples are generally mediated by expensive transition metal species. Herein, we describe the use of inexpensive and readily available tBuOK as a catalyst for P-P and P-E (E = O, S, or N) bond formation. Catalytic quantities of tBuOK in the presence of imine, azobenzene hydrogen acceptors, or a stoichiometric amount of tBuOK with hydrazobenzene, allow efficient homodehydrocoupling of phosphines under mild conditions (e.g. 25 °C and < 5 min). Further studies demonstrate that the hydrogen acceptors play an intimate mechanistic role. We also show that our tBuOK catalysed methodology is general for the heterodehydrocoupling of phosphines with alcohols, thiols and amines to generate a range of potentially useful products containing P-O, P-S, or P-N bonds.

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Nat Commun Asunto de la revista: BIOLOGIA / CIENCIA Año: 2019 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Nat Commun Asunto de la revista: BIOLOGIA / CIENCIA Año: 2019 Tipo del documento: Article