ChemInform Abstract: DIE SYNTH. UND DAS VOLTAMPEROMETRISCHE VERH. DER AMINOMETHYLDERIVATE DES 2,2‐DI‐(4‐HYDROXYPHENYL)‐PROPANS

Kuliev, A. M.; Kyazimova, R. K.; Mamedov, F. N.; Bairamova, A. G.; Agaeva, E. A.

doi:10.1002/chin.197232250

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Carboxylic Acids Esters Amides and Nitriles1

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1974

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“…Aliphatic-Aromatic Amines. Polarographic data are reported for catecholamines (318), for aminomethyl derivatives of 2,2-di(4-hydroxyphenyl)-propane (637), aryl aziridinium ions (557), 2,2,6,6-tetramethylpiperidinenitroxide and tert-butylnitroxide (1114), several iminoxyl radicals (631), and diastereoisomeric sympathomimetric amines (298). The reduction mechanism for 7 different imines in MeCN-DMF was reported (18).…”

Section: Carboxylic Acids Esters Amides and Nitrilesmentioning

confidence: 99%

Organic polarography

Pietrzyk¹

1974

Anal. Chem.

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Chemical Titles, and readily available journals ending November 30, 1973. This period has seen a continued growth in the use of polarography and related electrochemical techniques to follow chemical reactions and to supplement other physical and spectral measurements for purposes of characterization. Interest in applications toward biochemical and pharmaceutical problems has also increased. There also appears to be renewed interest in utilizing polarographic and related electrochemical data to predict and follow organoelectrochemical synthesis.In this review the symbols cv, dc, ac, and op are used to identify cyclic voltammetry, direct current polarography, alternating current polarography, and oscillographic polarography, respectively. Also, no attempt was made to list all organic polarographic references.

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Section: Carboxylic Acids Esters Amides and Nitrilesmentioning

confidence: 99%