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c Condensation of Bromoesters with the Sodium Derivatives
e Physical Properties
ix Magnetic Susceptibility x Optical Rotation
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9-decine-l-carboxylic a/3-acetylenic acids a/3-acetylenic esters acetic acid acetylenedicarboxylic acid acetylenedicarboxylic ester acetylenic acids acetylenic esters acid was obtained addition of bromine addition of hydrogen addition of iodine addition products adduct alcoholic potassium hydroxide alcoholic solution aliphatic alkali Amer amides ammonia anhydride aqueous solution Baeyer behenolic acid Bull carbon dioxide carboxylic catalyst CCOOH Chem chim cis isomer Comptes rend condensation COOEt COOH COOMe COOMe cyclisation decarboxylation described diacetylenic dicarboxylic acid Diels-Alder dimethyl acetylenedicarboxylate ester ethylenic ethylenic acids formation formed Friedldnder gave Grignard heating hydration hydrazine hydrogen bromide hydrogen chloride hydrogen halide hydrolysis ibid iodide isolated ketone methanol method methyl Michael mixture molecule Moureu and Delange nitriles o-nitrophenylpropiolic acid oxidation palladium phenyl phenylpropiolic acid phenylpropiolic ester potassium hydroxide prepared presence propiolic acid pyridine pyrrole Reactions involving rearrangement reduction Ruhemann salt sodium derivative solvent stearolic acid sulphuric acid tetrolic ester trans triple bond yield Zentr