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. Author manuscript; available in PMC: 2008 Aug 26.
Published in final edited form as: Chem Rev. 2007 May 27;107(6):2503–2545. doi: 10.1021/cr0509556

Table 51.

Solvent-free MBH reaction catalyzed by organocatalysts A – C and DABCO (20 mol% each) from Figure 50.

entrya product cat yield (%) ee (%)
1 graphic file with name nihms-63649-t0159.jpg A 65b 77
2 C quantc 60
3 graphic file with name nihms-63649-t0160.jpg A quantc 38
4 C 65c 34
5 graphic file with name nihms-63649-t0161.jpg A 35c 79
6 C 79c 50
7 graphic file with name nihms-63649-t0162.jpg A 62c 90
8 graphic file with name nihms-63649-t0163.jpg A 28c 79
9 C 52b 69
10 graphic file with name nihms-63649-t0164.jpg C quantb rac
11 graphic file with name nihms-63649-t0165.jpg C 22b 58
12 graphic file with name nihms-63649-t0166.jpg C quantb rac
13 graphic file with name nihms-63649-t0167.jpg B 47c 22
a

The reaction was carried out with 1 equiv of aldehyde and 4 equiv of enone or acrylate in the presence of 20 mol% catalyst and DABCO at 10°C for 72 h.

b

GC yield.

c

Isolated yield.