| Document Date: 2013-08-23 15:27:05
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City Voogd / Weinheim / Patil / / Company Simonovich S. P. / Merck / King A. E. / Strotman N. A. / Amgen / Ryland / MacMillan / Williamson A. E. / Allen A. E. / ASSOCIATED CONTENT / / Country United States / Monaco / / Currency pence / / / Facility Princeton University / / IndustryTerm metal / chemical synthesis / β-branched products / chemical reactions / organocatalytic α-alkenylation protocols / room temperature protocol / catalytic systems / trivial protocol / natural products / copper transition-metal catalyst / chemical correlation / αalkenyl aldehyde product / metal catalyst / synergistic protocol / / Organization David W. C. MacMillan* Merck Center for Catalysis / Princeton University / / Person Jason M. Stevens / Dalton Trans / Van Humbeck / / Position AUTHOR INFORMATION Corresponding Author dmacmill@princeton.edu Notes The authors / / ProvinceOrState New Jersey / Northern Territory / / Technology asymmetric / organocatalytic α-alkenylation protocols / operationally trivial protocol / room temperature protocol / coupling protocol / / URL http /
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Communication pubs.acs.org/JACS Enantioselective α‑Alkenylation of Aldehydes with Boronic Acids via the Synergistic Combination of Copper(II) and Amine Catalysis Jason M. Stevens and David W. C. MacMillan*