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Coviello DA, El-Fatatry HM. Chelating properties of alpha-oximinocarboxamides-I alpha-Oximinophenylacetamide isomers. Talanta. 1971;18(6):631-4doi: 10.1016/0039-9140(71)80094-2.
Coviello, D. A., & El-Fatatry, H. M. (1971). Chelating properties of alpha-oximinocarboxamides-I alpha-Oximinophenylacetamide isomers. Talanta, 18(6), 631-4. https://doi.org/10.1016/0039-9140(71)80094-2
Coviello, D A, and El-Fatatry, H M. "Chelating properties of alpha-oximinocarboxamides-I alpha-Oximinophenylacetamide isomers." Talanta vol. 18,6 (1971): 631-4. doi: https://doi.org/10.1016/0039-9140(71)80094-2
Coviello DA, El-Fatatry HM. Chelating properties of alpha-oximinocarboxamides-I alpha-Oximinophenylacetamide isomers. Talanta. 1971 Jun;18(6):631-4. doi: 10.1016/0039-9140(71)80094-2. PMID: 18960921.
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Talanta. 1971 Jun;18(6):631-4. doi: 10.1016/0039-9140(71)80094-2.

Chelating properties of alpha-oximinocarboxamides-I alpha-Oximinophenylacetamide isomers.

Talanta

D A Coviello, H M El-Fatatry

Affiliations

  1. Department of Chemistry, College of Pharmacy University of Illinois at the Medical Center Chicago, Illinois 60612 U.S.A.

PMID: 18960921 DOI: 10.1016/0039-9140(71)80094-2

Abstract

Various polyfunctional oximes chelate with metals pro vided that the other functional group is proximal to the oxime and contains a good donor atom or is a good donor itself. Thus alpha-oximinocarboxamides are potential chelating agents of analytical value since the amide function attached to the carbon atom bearing the oxime has two groups capable of functioning as donors (ketone and amine). Two isomers of alpha-oximinophenylacetamide (AOPA) were obtained by two different synthetic routes, and structures were assigned by spectrometric methods. syn-AOPA was found to have chelating properties, but the anti-isomer did not. The synthesis and details of structure assignments are reported here.

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