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. 2011 Aug 27;67(43):8353–8359. doi: 10.1016/j.tet.2011.08.058

Table 3.

Epoxidation of alkenes using 2

Entry Substrate Product Yielda (%)
1 graphic file with name fx3.gif graphic file with name fx4.gif 93 (70b, 58c)
2 graphic file with name fx5.gif graphic file with name fx6.gif 79
3 graphic file with name fx7.gif graphic file with name fx8.gif 85
4 graphic file with name fx9.gif graphic file with name fx10.gif 75
5 graphic file with name fx11.gif graphic file with name fx12.gif 72
6 graphic file with name fx13.gif graphic file with name fx14.gif 88 (70b)
a

Yield of isolated product.

b

Solution-phase reaction yield using 2-(phenylsulfonyl)-3-(p-nitrophenyl)oxaziridine (2 equiv), CHCl3, 60 °C, 12 h (Ref. 25).

c

Using polymer 1 (2 equiv), μW, 100 °C, CH2Cl2. Reaction was incomplete.