@article { ISI:000333477400027,
	title = {DMAP Promoted Tandem Addition Reactions Forming Substituted Tetrahydroxanthones},
	journal = {ORGANIC LETTERS},
	volume = {16},
	number = {6},
	year = {2014},
	month = {MAR 21},
	pages = {1642-1645},
	abstract = {Substituted tetrahydroxanthones are constructed using a DMAP-promoted tandem nucleophilic addition process. The reaction yields range from 39\% to 73\%. Disubstituted tetrahydroxanthones are generated as a similar to 2.3:1 mixture of diastereomers favoring the formation of the trans-isomer.},
	issn = {1523-7060},
	doi = {10.1021/ol5002945},
	author = {Castillo-Contreras, Emmanuel B. and Dake, Gregory R.}
}
