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. Author manuscript; available in PMC: 2008 Feb 12.
Published in final edited form as: Tetrahedron Lett. 2007 Feb 12;48(7):1295–1298. doi: 10.1016/j.tetlet.2006.12.005

Table 2.

Isoxazoles formed from the 1,3-dipolar cycloaddition reactions using sulfone and sulfoxide containing bromoalkenes as the dipolarophile.

Entry Alkene α-Chloro oxime Product % Yield
7 graphic file with name nihms-16926-t0020.jpg graphic file with name nihms-16926-t0021.jpg graphic file with name nihms-16926-t0022.jpg 91
8 graphic file with name nihms-16926-t0023.jpg graphic file with name nihms-16926-t0024.jpg graphic file with name nihms-16926-t0025.jpg 85
9 graphic file with name nihms-16926-t0026.jpg graphic file with name nihms-16926-t0027.jpg graphic file with name nihms-16926-t0028.jpg 81
10 graphic file with name nihms-16926-t0029.jpg graphic file with name nihms-16926-t0030.jpg graphic file with name nihms-16926-t0031.jpg 91
11 graphic file with name nihms-16926-t0032.jpg graphic file with name nihms-16926-t0033.jpg graphic file with name nihms-16926-t0034.jpg 69
12 graphic file with name nihms-16926-t0035.jpg graphic file with name nihms-16926-t0036.jpg graphic file with name nihms-16926-t0037.jpg 71