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. Author manuscript; available in PMC: 2014 Aug 15.
Published in final edited form as: Tetrahedron Lett. 2013 Jun 18;54(33):4463–4466. doi: 10.1016/j.tetlet.2013.06.041

Table 1.

Catalytic oxidative carbon-carbon bond cleavage of glycerol with various oxidizing agents in the presence of Pd catalysts at room temperature.a

entry catalyst oxidant yield (%)d 2/3 (× 10−5 mol)e
1 PdCl2 H2O2 trace trace/trace
2 Pd(OAc)2 H2O2 6 0.16/0.20
3 4 H2O2 41 1.50/8.05
4 4 t-BuO2H trace -/-
5b 4 Oxone 10 0.39/1.52
6 4 K2S2O8 - -/-
7c 4 O2 - -/-
a

All reactions were performed with glycerol (10 mg, 10.8 × 10−5 mol), Pd catalyst (5 mol%). Entry 1–3: 30% H2O2 (0.4 mL) in H2O (0.1 mL) was added. In the entry 4, tBuOOH (70% in H2O, 0.4 mL) was used. Entries 5~6: 10.8 × 10−5 mol of oxidant (entry 5: oxone, entry 6: K2S2O8) in 0.3 mL of H2O was used. Entry 7: O2 was bubbled in 0.3 mL of H2O solution. All reactions were performed at room temperature for 6 hours..

b

Run in H2O (0.4 mL).

c

Continuous flow with O2.

d

Conversion yield of glycerol.

e

The amount of each product was determined by 1H NMR spectral analysis using MeOH as the internal standard.8