| Document Date: 2013-07-26 15:57:06
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City Weinheim / London / New York / Jui / Oxford / / Company Fleming / Porter N. A. / Merck / Cyclic Systems / Amgen / Shimizu / Heterocyclic Systems / Suzuki / MacMillan / Brown S. P. / ASSOCIATED CONTENT / / Country United States / / / Facility Princeton University / / IndustryTerm type products / delivered ring systems / catalytic enantioselective carbonyl-ene protocols / homo-ene technology / olefin systems / enantioenriched cyclized product / chemical synthesis community / chemical correlation / organocatalytic protocol / bicyclic products / / Organization David W. C. MacMillan* Merck Center for Catalysis / Princeton University / Royal Society of Chemistry / / Person Beeson / Fernanda G. Finelli / / Position AUTHOR INFORMATION Corresponding Author dmacmill@princeton.edu Notes The authors / T. D. / / ProvinceOrState New Jersey / Northern Territory / / Technology catalytic enantioselective carbonyl-ene protocols / drug discovery / two-step organocatalytic protocol / SOMO-mediated homo-ene technology / / URL http /
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Communication pubs.acs.org/JACS Enantioselective Intramolecular Aldehyde α‑Alkylation with Simple Olefins: Direct Access to Homo-Ene Products Robert J. Comito, Fernanda G. Finelli, and David W. C. MacMillan*