. 2017 Nov 30;2(11):8507–8516. doi: 10.1021/acsomega.7b01637

Table 2. Rh(III)-Catalyzed Reactions of Various Cyclic 2-Diazo-1,3-diketones and N-Arylacetamides^a^,^b.

Reaction conditions: cyclic 2-dizao-1,3-diketone 1 (0.5 mmol), N-arylacetamides 2 (0.5 mmol), [Cp*RhCl₂]₂ (1 mol %), and AgNTf₂ (10 mol %) in DCE (3 mL) were stirred at reflux for 12 h.

Isolated yield.

Table 2. Rh(III)-Catalyzed Reactions of Various Cyclic 2-Diazo-1,3-diketones and N-Arylacetamidesa,b.

Table 2. Rh(III)-Catalyzed Reactions of Various Cyclic 2-Diazo-1,3-diketones and N-Arylacetamides^a^,^b.