@article {107786,
	title = {Enantioselective total synthesis of hyperforin.},
	journal = {J Am Chem Soc},
	volume = {135},
	year = {2013},
	month = {2013 Jan 16},
	pages = {644-7},
	abstract = {A modular, 18-step total synthesis of hyperforin is described. The natural product was quickly accessed using latent symmetry elements, whereby a group-selective, Lewis acid-catalyzed epoxide-opening cascade cyclization was used to furnish the bicyclo[3.3.1]nonane core and set two key quaternary stereocenters.},
	keywords = {Bicyclo Compounds, Cyclization, Lewis Acids, Molecular Structure, Phloroglucinol, Stereoisomerism, Terpenes},
	issn = {1520-5126},
	doi = {10.1021/ja312150d},
	author = {Sparling, Brian A and Moebius, David C and Shair, Matthew D.}
}
