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. 2017 Nov 3;23(66):16853–16861. doi: 10.1002/chem.201703609

Table 2.

Catalytic hydroboration of aldehydes and ketones using 1tLi precatalyst in C6D6.

Aldehyde/Ketone t [h] Yield as determined by 1H NMR [%][a]
1 graphic file with name CHEM-23-16853-g013.jpg 0.25 >99 [>95][c]
2 graphic file with name CHEM-23-16853-g014.jpg 0.25 93
3 graphic file with name CHEM-23-16853-g015.jpg 0.25 98
4 graphic file with name CHEM-23-16853-g016.jpg 0.25 >99
5 graphic file with name CHEM-23-16853-g017.jpg 0.25 >99
6 [b] graphic file with name CHEM-23-16853-g018.jpg 24 >99
7 graphic file with name CHEM-23-16853-g019.jpg 0.5 97
8 graphic file with name CHEM-23-16853-g020.jpg 0.25 >99
9 graphic file with name CHEM-23-16853-g021.jpg 0.25 >99
10 graphic file with name CHEM-23-16853-g022.jpg 0.25 >99
11 graphic file with name CHEM-23-16853-g023.jpg 0.25 97
12 graphic file with name CHEM-23-16853-g024.jpg 0.25 >98
13 [b] graphic file with name CHEM-23-16853-g025.jpg 24 89
14 graphic file with name CHEM-23-16853-g026.jpg 0.25 96
15 [b] graphic file with name CHEM-23-16853-g027.jpg 24 69

[a] Yield determined by formation of RR'CHOBpin relative to internal standard hexamethylcyclotrisiloxane. [b] Heated at 70 °C. [c] 1 % catalyst loading.