Expanding the scope of the Cu assisted Suzuki–Miyaura reaction

Recent advances in the development of the copper facilitated Suzuki–Miyaura reaction are described. Improvements include expansion of substrate scope to include aryl chlorides and polyhalo aryl boronates. It was found that use of S-Phos and X-Phos could accomplish the coupling of 2-pyridyl boronates...

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Veröffentlicht in:Tetrahedron letters 2011-09, Vol.52 (39), p.5055-5059
Hauptverfasser: Crowley, Brendan M., Potteiger, Craig M., Deng, James Z., Prier, Christopher K., Paone, Daniel V., Burgey, Christopher S.
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container_end_page 5059
container_issue 39
container_start_page 5055
container_title Tetrahedron letters
container_volume 52
creator Crowley, Brendan M.
Potteiger, Craig M.
Deng, James Z.
Prier, Christopher K.
Paone, Daniel V.
Burgey, Christopher S.
description Recent advances in the development of the copper facilitated Suzuki–Miyaura reaction are described. Improvements include expansion of substrate scope to include aryl chlorides and polyhalo aryl boronates. It was found that use of S-Phos and X-Phos could accomplish the coupling of 2-pyridyl boronates to aryl chlorides and bromides in shorter reaction times and in higher yield than previously described with DPPF.
doi_str_mv 10.1016/j.tetlet.2011.07.088
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subjects 2-Pyridyl boronates
Aromatic compounds
Bromides
Chemical reactions
Chemistry
Chlorides
Copper
Copper assisted reaction
Exact sciences and technology
Heterocyclic compounds
Heterocyclic compounds with only one n hetero atom and condensed derivatives
Joining
Kinetics and mechanisms
Organic chemistry
Organometallic
Preparations and properties
Reaction time
Reactivity and mechanisms
S-Phos
Suzuki–Miyaura
Tetrahedrons
title Expanding the scope of the Cu assisted Suzuki–Miyaura reaction
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