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. 2016 Dec 9;148(1):3–35. doi: 10.1007/s00706-016-1883-7

Table 2.

One-pot procedure for the synthesis of 1,6-naphthyridin-2(1H)-ones [4]

Entry Ar1B(OR)2 Time Ar2B(OR)2 Time/h Yield/%a
1b graphic file with name 706_2016_1883_Figh_HTML.gif 3 h graphic file with name 706_2016_1883_Figm_HTML.gif 2 51
2 graphic file with name 706_2016_1883_Figi_HTML.gif 10 min graphic file with name 706_2016_1883_Fign_HTML.gif 3 58
3 graphic file with name 706_2016_1883_Figj_HTML.gif 10 min graphic file with name 706_2016_1883_Figo_HTML.gif 2 55
4 graphic file with name 706_2016_1883_Figk_HTML.gif 1.25 h graphic file with name 706_2016_1883_Figp_HTML.gif 1.5 32
5 graphic file with name 706_2016_1883_Figl_HTML.gif 1.5 h graphic file with name 706_2016_1883_Figq_HTML.gif 3.5 33

aIsolated yield after purification

bMonocoupled product was isolated before the second step