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Lithium aluminium hydride / Aldehyde / Wolff–Kishner reduction / Sodium borohydride / Carboxylic acid / Hydrogenation / Alcohol / Nitrile / Chemistry / Functional groups / Reducing agents


Myers Chem 215
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Document Date: 2007-03-31 12:14:26

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City

EtOH CH3O2C / Washington DC / Yoon / Ponndorf / Burke / New York / /

Company

Fleming / Miller A. E. / Cox / Pergamon Press / Kende A. S. / Plenum Press / John Wiley and Sons / Bernstein / /

Country

Ireland / /

Event

FDA Phase / /

Facility

THF complex / D O Garner / /

IndustryTerm

metal / by-products / reduction product / aldehyde product / /

Movie

A. D. / /

Organization

American Chemical Society / /

Person

Mark G. Charest Ester Aldehyde / Kopecky / CHO DIBAL / Ester Amide Carboxylate Salt Amine / Mark G. Charest Reductive / Mark G. Charest Wolff / Mark G. Charest Aldehyde / Aicher / Jason Brubaker Aldehyde / Kennedy / Mark G. Charest Lithium Triethoxyaluminohydride / Madar / Ion Acid Halide Aldehyde Ester / Mark G. Charest / /

Position

D. J. / R. D. J. / H. D. J. / V. P. / Reduction General / T. D. / /

Product

reduction / /

ProgrammingLanguage

DC / /

ProvinceOrState

South Dakota / New Mexico / Mississippi / /

PublishedMedium

Aldrichimica Acta / /

Technology

Rosemund protocol / ATM / /

SocialTag