Influence of the chalcogenocarbonyl group on the structure of heterocyclic analogues of β-tricarbonyl compounds. Synthesis and structural features of Schiff bases derived from 3-formyl-4-thio(seleno)coumarin-Reference-Cited by-同舟云学术

Influence of the chalcogenocarbonyl group on the structure of heterocyclic analogues of β-tricarbonyl compounds. Synthesis and structural features of Schiff bases derived from 3-formyl-4-thio(seleno)coumarin

Published:1993 Issue:12 Volume: Page:2423-2428
ISSN:0300-9580
Container-title:J. Chem. Soc., Perkin Trans. 2
language:en
Short-container-title:J. Chem. Soc., Perkin Trans. 2

Author:

Nivorozhkin Alexander L.,Toftlund Hans,Stein Paul C.,Jensen Frank

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/1993/P2/P29930002423

Reference28 articles.

1. Nmr spectroscopic studies on the tautomerism in tenuazonic acid analogs

2. NMR Spectroscopic Studies on the Tautomerism in Schiff Bases of Tenuazonic Acid Analogs

3. Nuclear magnetic resonance spectroscopic studies on the tautomerism in tetramic acid analogues and their anilides. Part 4. Interpretation of carbon-13 spectra by molecular orbital calculations

4. 1H, 13C, and 15N nuclear magnetic resonance studies on the tautomerism of the Schiff's bases of 3-acetyl-6-methyl-2H-pyran-2,4(3H)-dione and 3,5-diacetyltetrahydropyran-2,4,6-trione

5. Reaktionen an Heterocyclen mit 2-Acyl-2-propenon-Teilstruktur, 6. Mitt. Zur Synthese von 6-Oxo-6H-[1]benzopyrano[4,3-b]chinolinen

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