Chem. Rev. 2010, 110, 1435 1462
Transcript of Chem. Rev. 2010, 110, 1435 1462
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Chem. Rev. 2010, 110, 1435–1462
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Chem. Rev. 2010, 110, 1435–1462
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K. Inamoto et al. JOC, 2009, 694, 389–396
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K. Inamoto et al. JOC, 2009, 694, 389–396
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David J. Michaelis et al. Acs Catal. 2018, 8, 86-89
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David J. Michaelis et al. Acs Catal. 2018, 8, 86-89
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David J. Michaelis et al. Acs Catal. 2018, 8, 86-89
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310 mg
1 mmol
300 mg
1.3 mmol 500 mg
Yield : 92 %
120°C
3 h
David J. Michaelis et al. Acs Catal. 2018, 8, 86-89
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270 mg
0.5 mmol
+
61 mg
0.65 mmol
THF 5 mL
6 h, r.t
Methylallyl nickel
chloride dimer
in 3 mL toluene
75 mg 0.25 mmol
+
puffy white solid
in 2 mL toluene
250 mg 0.5 mmol
2 h, r.t.
puffy white solid
(226 mg, Yield : 90 %)
(260 mg, Yield : 80 % )
David J. Michaelis et al. Acs Catal. 2018, 8, 86-89
dissolved in
benzene/Hexane
(V:V, 2:11)
and passed
through celite
dissolved in
benzene
and passed
through celite
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J. Am. Chem. Soc. 2015, 137, 15600–15603
Evaluation of Catalysts for Synthesis of 1,1,1- Tris(boronate) 1oa from Styrene and B2pin2
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J. Am. Chem. Soc. 2015, 137, 15600–15603
Co-Catalyzed Synthesis of 1,1,1-Tris(boronates) from Various Vinylarenes
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Future work