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Catalysis / Substitution reactions / Organic chemistry / Organocatalysis / Tsuji–Trost reaction / Nucleophilic conjugate addition / Transfer hydrogenation / Carroll rearrangement / Chemistry / Organic reactions / Palladium


Direct and enantioselective α-allylation of ketones via singly occupied molecular orbital (SOMO) catalysis Anthony Mastracchio, Alexander A. Warkentin, Abbas M. Walji, and David W. C. MacMillan1 Merck Center for Catalys
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Document Date: 2011-01-03 12:57:37

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City

Cambridge / Wallingford / New York / /

Company

Merck / Amgen / Northrup AB / Gaussian Inc. / Stephens / Ma S (2008) Metal / MacMillan / Doyle AG / /

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Facility

Princeton University / National Institute of General Medical Sciences / Harvard University / /

IndustryTerm

heteroaryl systems / furan methyl / chemical synthesis / metal enolates / catalytic protocol / chemical formula / alkylation product / crude product / /

MusicGroup

C.M. / /

Organization

Harvard University / David W. C. MacMillan1 Merck Center for Catalysis / Princeton University / National Institute of General Medical Sciences / /

Person

Anthony Mastracchio / Alexander A. Warkentin / Abbas M. Walji / Hui-Wen Shih / /

Position

Author / representative / General / /

ProvinceOrState

New Jersey / New York / Massachusetts / Connecticut / /

RadioStation

Harned AM / /

SportsEvent

formula 1 / /

Technology

condensation / catalytic protocol / flash / /

URL

www.pnas.org/lookup/suppl / www.pnas.org/cgi/doi/10.1073/pnas.1002845107 / /

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