@article { ISI:000339983300052,
	title = {Annulated Isoxazoles via {[}3+2] Cycloaddition of Alkenyl Bromides and Oximoyl Chlorides and Ag(I) Promoted Elimination},
	journal = {JOURNAL OF ORGANIC CHEMISTRY},
	volume = {79},
	number = {15},
	year = {2014},
	month = {AUG 1},
	pages = {7250-7255},
	abstract = {Substituted salicylaldehydes are converted to fused tetracyclic isoxazoles through a synthetic sequence incorporating substitution of 2-bromo-2-cyclohexen-1-ol, formation of an oxime function, conversion to an oximoyl chloride, intramolecular {[}3 + 2] cycloaddition, and elimination of an equivalent of hydrogen bromide using silver(I) carbonate. Six examples of this sequence are presented.},
	issn = {0022-3263},
	doi = {10.1021/jo501376q},
	author = {Castillo-Contreras, Emmanuel B. and Stahl, Alexander M. and Dake, Gregory R.}
}
