Experimental and computational insights into the mechanism of the copper(i)-catalysed sulfonylative Suzuki-Miyaura reaction
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作者:
Hall, Callum G. J.
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GlaxoSmithKline, Med Design, Gunnels Wood Rd, Stevenage SG1 2NY, England
Univ Strathclyde, Dept Pure & Appl Chem, 295 Cathedral St, Glasgow G1 1XL, ScotlandGlaxoSmithKline, Med Design, Gunnels Wood Rd, Stevenage SG1 2NY, England
Hall, Callum G. J.
[1
,2
]
Sneddon, Helen F. F.
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GlaxoSmithKline, Med Design, Gunnels Wood Rd, Stevenage SG1 2NY, England
Univ York, Green Chem Ctr Excellence, Dept Chem, York YO10 5DD, EnglandGlaxoSmithKline, Med Design, Gunnels Wood Rd, Stevenage SG1 2NY, England
Sneddon, Helen F. F.
[1
,3
]
Pogany, Peter
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GlaxoSmithKline, Med Design, Gunnels Wood Rd, Stevenage SG1 2NY, EnglandGlaxoSmithKline, Med Design, Gunnels Wood Rd, Stevenage SG1 2NY, England
Pogany, Peter
[1
]
Lindsay, David M.
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Univ Strathclyde, Dept Pure & Appl Chem, 295 Cathedral St, Glasgow G1 1XL, ScotlandGlaxoSmithKline, Med Design, Gunnels Wood Rd, Stevenage SG1 2NY, England
Lindsay, David M.
[2
]
Kerr, William J.
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Univ Strathclyde, Dept Pure & Appl Chem, 295 Cathedral St, Glasgow G1 1XL, ScotlandGlaxoSmithKline, Med Design, Gunnels Wood Rd, Stevenage SG1 2NY, England
Kerr, William J.
[2
]
机构:
[1] GlaxoSmithKline, Med Design, Gunnels Wood Rd, Stevenage SG1 2NY, England
A mechanistic study into the copper(i)-catalysed sulfonylative Suzuki-Miyaura reaction, incorporating sulfur dioxide, is described. Utilising spectroscopic and computational techniques, an exploration into the individual components of the competing catalytic cycles is delineated, including identification of the resting state catalyst, transmetalation of arylboronic acid onto copper(i), the sulfur dioxide insertion process, and the oxidative addition of aryl halide to Cu-I. Studies also investigated prominent side-reactions which were uncovered, including a competing copper(ii)-catalysed mechanism. This led to an additional proposed and connected Cu-I/Cu-II/Cu-III catalytic cycle to account for by-product formation.