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. Author manuscript; available in PMC: 2015 Mar 1.
Published in final edited form as: Org Chem Front. 2014 Mar;1(1):34–38. doi: 10.1039/C3QO00080J

Table 3. Scope with substrates derived from acyclic enones/enals[a,b].

graphic file with name nihms599293u6.jpg
1 graphic file with name nihms599293t10.jpg 2 graphic file with name nihms599293t11.jpg 3 graphic file with name nihms599293t12.jpg
4a, 6h, 91% 4b,10h, 88% 4c, 2.5h, 80%
4 graphic file with name nihms599293t13.jpg 5 graphic file with name nihms599293t14.jpg 6 graphic file with name nihms599293t15.jpg
4d, 6h, 90% 4e, 1.5h, 92% 4f, 4.5h, 95%
7[b] graphic file with name nihms599293t16.jpg 8 graphic file with name nihms599293t17.jpg 9 graphic file with name nihms599293t18.jpg
4g, 10h, 70% 4h, 10h, 85% 4i, 10h, 85%
10 graphic file with name nihms599293t19.jpg
4j, 3h, 94%
[a]

Initially [1] = 0.1 M.

[b]

Isolated yields are shown.