Download - Chem. Rev. 2010, 110, 1435 1462
Chem. Rev. 2010, 110, 1435–1462
Chem. Rev. 2010, 110, 1435–1462
K. Inamoto et al. JOC, 2009, 694, 389–396
K. Inamoto et al. JOC, 2009, 694, 389–396
David J. Michaelis et al. Acs Catal. 2018, 8, 86-89
David J. Michaelis et al. Acs Catal. 2018, 8, 86-89
David J. Michaelis et al. Acs Catal. 2018, 8, 86-89
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
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
J. Am. Chem. Soc. 2015, 137, 15600–15603
Evaluation of Catalysts for Synthesis of 1,1,1- Tris(boronate) 1oa from Styrene and B2pin2
J. Am. Chem. Soc. 2015, 137, 15600–15603
Co-Catalyzed Synthesis of 1,1,1-Tris(boronates) from Various Vinylarenes
Future work