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. 2010 Feb 8;107(8):3373–3376. doi: 10.1073/pnas.0913466107

Table 2.

Tandem CM-furan formation: scope of the allylic alcohol component

graphic file with name pnas.0913466107figX14.jpg
Entry Allylic Alcohol Product Yield, %
1 graphic file with name pnas.0913466107figX15.jpg graphic file with name pnas.0913466107figX16.jpg 76
2* graphic file with name pnas.0913466107figX17.jpg graphic file with name pnas.0913466107figX18.jpg 61
3 graphic file with name pnas.0913466107figX19.jpg graphic file with name pnas.0913466107figX20.jpg 53
4 graphic file with name pnas.0913466107figX21.jpg graphic file with name pnas.0913466107figX22.jpg 65
5 graphic file with name pnas.0913466107figX23.jpg graphic file with name pnas.0913466107figX24.jpg 51
6 graphic file with name pnas.0913466107figX25.jpg graphic file with name pnas.0913466107figX26.jpg 36

*The reaction was run at 70 °C.

The reaction was run at 0.17 M.

Phenyl vinyl ketone was employed as the enone component and the reaction was run at 60 °C.