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. 2010 Oct 25;107(48):20661–20665. doi: 10.1073/pnas.1007469107

Table 2.

NHC-catalyzed reactions of alpha-hydroxy ketoenonegraphic file with name pnas.1007469107figX3.jpg

Entry R1 = % yield* d.r. % ee
1 Ph 93 > 20∶1 99
2 p-BrC6H4 93 > 20∶1 99
3 p-MeOC6H4 92 > 20∶1 99
4 2-furyl 85 > 20∶1 99
5 p-CHOC6H4 96 > 20∶1 99
6 H 89 > 20∶1 99

*Isolated yield following chromatography.

Determined by 1H NMR of unpurified reaction mixtures.

Determined by SFC analysis on chiral stationary phases. SFC, supercritical fluid chromatography.