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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 1.

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

Entry Alkene α-Chloro oxime Product % Yield
1 graphic file with name nihms-16926-t0002.jpg graphic file with name nihms-16926-t0003.jpg graphic file with name nihms-16926-t0004.jpg 79
2 graphic file with name nihms-16926-t0005.jpg graphic file with name nihms-16926-t0006.jpg graphic file with name nihms-16926-t0007.jpg 68
3 graphic file with name nihms-16926-t0008.jpg graphic file with name nihms-16926-t0009.jpg graphic file with name nihms-16926-t0010.jpg 64
4 graphic file with name nihms-16926-t0011.jpg graphic file with name nihms-16926-t0012.jpg graphic file with name nihms-16926-t0013.jpg 75
5 graphic file with name nihms-16926-t0014.jpg graphic file with name nihms-16926-t0015.jpg graphic file with name nihms-16926-t0016.jpg 80
6 graphic file with name nihms-16926-t0017.jpg graphic file with name nihms-16926-t0018.jpg graphic file with name nihms-16926-t0019.jpg 80