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. Author manuscript; available in PMC: 2010 Jan 3.
Published in final edited form as: Tetrahedron. 2009 Jan 3;65(1):70–76. doi: 10.1016/j.tet.2008.10.019

Table 3.

Methylene epoxidations using sulfonium salt 1.

graphic file with name nihms83407f12.jpg
entry carbonyl derivative yield (%)a entry carbonyl derivative yield (%)a
1, a graphic file with name nihms83407t8.jpg 97 6, f graphic file with name nihms83407t9.jpg 86
2, b graphic file with name nihms83407t10.jpg 97 7, g graphic file with name nihms83407t11.jpg 92
3, c graphic file with name nihms83407t12.jpg 98 8, h graphic file with name nihms83407t13.jpg 91
4, d graphic file with name nihms83407t14.jpg 95 9, i graphic file with name nihms83407t15.jpg 95
5, e graphic file with name nihms83407t16.jpg 93 10, j graphic file with name nihms83407t17.jpg 86
a

Isolated chromatographically pure material.