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. 2017 May 4;13:817–824. doi: 10.3762/bjoc.13.82

Table 2.

Substrate scope for the syntheses of compounds 4 and 6.a

Entry Starting materials GBB product 4 Yieldb (%) Cyclized product 6 Yieldb (%)

1 graphic file with name Beilstein_J_Org_Chem-13-817-i002.jpg Inline graphic
4b
94 Inline graphic
6b
72
2 graphic file with name Beilstein_J_Org_Chem-13-817-i005.jpg Inline graphic
4c
80 Inline graphic
6c
75
3 graphic file with name Beilstein_J_Org_Chem-13-817-i008.jpg Inline graphic
4d
62 Inline graphic
6d
61
4 graphic file with name Beilstein_J_Org_Chem-13-817-i011.jpg Inline graphic
4e
96 Inline graphic
6e
63
5 graphic file with name Beilstein_J_Org_Chem-13-817-i014.jpg Inline graphic
4f
89 Inline graphic
6f
78
6 graphic file with name Beilstein_J_Org_Chem-13-817-i017.jpg Inline graphic
4g
61 Inline graphic
6g
80
7 graphic file with name Beilstein_J_Org_Chem-13-817-i020.jpg Inline graphic
4h
85 Inline graphic
6h
56
8 graphic file with name Beilstein_J_Org_Chem-13-817-i023.jpg Inline graphic
4i
88 Inline graphic
6i
58
9 graphic file with name Beilstein_J_Org_Chem-13-817-i026.jpg Inline graphic
4j
64 Inline graphic
6j
78
10 graphic file with name Beilstein_J_Org_Chem-13-817-i029.jpg Inline graphic
4k
75 Inline graphic
6k
87
11 graphic file with name Beilstein_J_Org_Chem-13-817-i032.jpg Inline graphic
4l
49 Inline graphic
6l
79
12 graphic file with name Beilstein_J_Org_Chem-13-817-i035.jpg Inline graphic
4m
71 Inline graphic
6m
48
13 graphic file with name Beilstein_J_Org_Chem-13-817-i038.jpg Inline graphic
4n
47 Inline graphic
6n
55
14 graphic file with name Beilstein_J_Org_Chem-13-817-i041.jpg Inline graphic
4o
54 Inline graphic
6o
62
15 graphic file with name Beilstein_J_Org_Chem-13-817-i044.jpg Inline graphic
4p
95 Inline graphic
6p
63
16 graphic file with name Beilstein_J_Org_Chem-13-817-i047.jpg Inline graphic
4q
74 Inline graphic
6q
58
17 graphic file with name Beilstein_J_Org_Chem-13-817-i050.jpg Inline graphic
4r
43 Inline graphic
6r
67
18 graphic file with name Beilstein_J_Org_Chem-13-817-i053.jpg Inline graphic
4s
57 Inline graphic
6s
59

aGBB reaction conditions: 1 (0.5 mmol), 2 (0.5 mmol), 3 (0.6 mmol), MeOH (1 mL); PTSA (5%), room temperature, 12h; annulation conditions: substrate 4 (0.2 mmol), Au(JohnPhos)Cl (10 mol %), CH3CN (2 mL) at reflux temperature for 24 h. bIsolated yields.