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. 2015 Jan 26;6(3):2010–2015. doi: 10.1039/c4sc03675a

Table 2. Hydrogenation of N-containing substrates catalyzed by 10b a .

Inline graphic
Entry Substrate Product Yield
1 graphic file with name c4sc03675a-u3.jpg graphic file with name c4sc03675a-u4.jpg 100 b (98)
2 graphic file with name c4sc03675a-u5.jpg graphic file with name c4sc03675a-u6.jpg 100 (82)
3 graphic file with name c4sc03675a-u7.jpg graphic file with name c4sc03675a-u8.jpg 39
4 graphic file with name c4sc03675a-u9.jpg graphic file with name c4sc03675a-u10.jpg 100 (71)
5 graphic file with name c4sc03675a-u11.jpg graphic file with name c4sc03675a-u12.jpg 100 (95)
6 graphic file with name c4sc03675a-u13.jpg graphic file with name c4sc03675a-u14.jpg 0
7 graphic file with name c4sc03675a-u15.jpg graphic file with name c4sc03675a-u16.jpg 100 (91)
8 graphic file with name c4sc03675a-u17.jpg graphic file with name c4sc03675a-u18.jpg 0
9 graphic file with name c4sc03675a-u19.jpg graphic file with name c4sc03675a-u20.jpg 100 (87)

aYields determined by 1H NMR spectroscopy, isolated yields in parentheses. All reactions were carried out using 0.500 mmol substrate in CH2Cl2. Reaction times were 30 minutes. Catalyst loadings: 5 mol% except:

b2.5 mol%.