@article {9819,
	title = {Tandem Phenolic Oxidative Amidation-Intramolecular Diels-Alder Reaction: An Approach to the Himandrine Core.},
	journal = {Organic Letters},
	volume = {12},
	year = {2010},
	note = {CAPLUS AN 2010:375458(Journal)},
	month = {2010///},
	pages = {1760 - 1763},
	publisher = {American Chemical Society},
	abstract = {An oxidative cyclization of dienic sulfonamides, e.g. I, mediated by iodobenzene diacetate in TFA, followed by a tandem intramol. Diels-Alder reaction, achieves desymmetrization of a "locally sym." dienone with good levels of diastereoselectivity and leads to valuable synthetic intermediates for the himandrine alkaloids, e.g. II. [on SciFinder(R)]},
	keywords = {phenolic oxidative amidation intramol Diels Alder himandrine intermediate},
	isbn = {1523-7060},
	author = {Liang,Huan and Ciufolini,Marco A.}
}
