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Please use this identifier to cite or link to this item: http://tainguyenso.vnu.edu.vn/jspui/handle/123456789/12975

Title: Isolation, structure, and properties of quinone-aci tautomer of a phenol-nitro compound related to eugenoxyacetic acid
Authors: Dinh N.H.
Huan T.T.
Toan D.N.
Kimpende P.M.
Meervelt L.V.
Keywords: Eugenoxyacetic acid
Nitro-aci tautomerization
Nitrophenol
Quinone
Tautomer
Issue Date: 2010
Publisher: Journal of Molecular Structure
Citation: Volume 980, Issue 3-Jan, Page 137-142
Abstract: Treatment with excess nitric acid in acetic acid revealed that eugenoxyacetic acid underwent an unexpected ether cleavage, a normal nitration, and then an unexpected electrophilic addition to the double bond of the side chain that led to the formation of a dinitro compound which subsequently converted to a sensitive, reactive quinone-aci compound. The structure of the quinone-aci compound (1) and its derivatives (2-6) was established by 1D- , 2D NMR, MS spectra, and chemical methods. In addition, the XRD structure of compound 2 derived from 1 was established. A double tautomerization of 1 in solution was studied by the LC-UV-MS method. © 2010 Elsevier B.V. All rights reserved.
URI: http://tainguyenso.vnu.edu.vn/jspui/handle/123456789/12975
ISSN: 222860
Appears in Collections:New - Articles of Universities of Vietnam from Scopus

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