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Spectroscopy / Nuclear magnetic resonance spectroscopy / Proton NMR / Vitexin / Nitrone-olefin 3+2 cycloaddition / Chemistry / Organic reactions / Nuclear magnetic resonance


Development of a general, enantioselective organocatalytic Mukaiyama-Michael reaction with α,β-unsaturated aldehydes
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Document Date: 2010-10-27 21:27:55


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City

Goodwin / Pasadena / Oxford / Weinheim / Heidelberg / /

Company

Hewlett-Packard / Amgen / Ethyl / CH(CH3)CO / Agilent / Merck / Perrin D. D. / Elsevier Ltd. / MacMillan / Brown S. P. / /

Country

Germany / United States / /

Currency

AMD / USD / /

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Event

FDA Phase / /

Facility

Princeton University / Laboratory Chemicals / California Institute of Technology Mass Spectrometer Facility / California Institute of Technology / /

IndustryTerm

colorless oil / syn-selective products / pure product / iminium catalysis protocol / online version / Gas chromatography / chemical shift / chemical tool / conjugate addition product / metal catalysis / syn product / chemical correlation / anti protocols / oil / crude product / gas chromatographs / title product / yellow oil / addition protocols / /

Organization

California Institute of Technology / q¼quartet / Princeton University / California Institute of Technology Mass Spectrometer Facility / MM3 force / Division of Chemistry and Chemical Engineering / /

Person

Michael Enantioselective / D.D. Turner / Christopher J. Borths / Elmer Paragon / Diane E. Carrera / Larry E. Overman / Lewis Acid / /

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Position

General Commercial reagents / scholar / teacher / OD-H guard / Corresponding author / great scientist / scholar / Professor / AD-H guard / /

Product

catalysis / /

ProvinceOrState

New Jersey / North Carolina / California / /

PublishedMedium

Aldrichimica Acta / /

Technology

Molecular modeling / X-ray / anti protocols / condensation / Gas chromatography / addition protocols / simulation / iminium catalysis protocol / Michael technology / /

URL

www.elsevier.com/locate/tet / /

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