enol

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e·nol

 (ē′nôl′, ē′nōl′)
n.
An organic compound containing a hydroxyl group bonded to a carbon atom, which in turn is doubly bonded to another carbon atom.

[From -en(e) + -ol.]

e·nol′ic (ē-nŏl′ĭk) adj.
American Heritage® Dictionary of the English Language, Fifth Edition. Copyright © 2016 by Houghton Mifflin Harcourt Publishing Company. Published by Houghton Mifflin Harcourt Publishing Company. All rights reserved.

enol

(ˈiːnɒl)
n
(Elements & Compounds) any organic compound containing the group -CH:CO-, often existing in chemical equilibrium with the corresponding keto form. See keto-enol tautomerism
[C19: from -ene + -ol1]
eˈnolic adj
Collins English Dictionary – Complete and Unabridged, 12th Edition 2014 © HarperCollins Publishers 1991, 1994, 1998, 2000, 2003, 2006, 2007, 2009, 2011, 2014

e•nol

(ˈi nɔl, ˈi nɒl)

n.
an organic compound containing a hydroxyl group attached to a doubly linked carbon atom.
[1935–40; appar. < Greek (h)én one (neuter) + -ol1]
e•nol•ic (iˈnɒl ɪk) adj.
Random House Kernerman Webster's College Dictionary, © 2010 K Dictionaries Ltd. Copyright 2005, 1997, 1991 by Random House, Inc. All rights reserved.
ThesaurusAntonymsRelated WordsSynonymsLegend:
Noun1.enol - an organic compound that contains a hydroxyl group bonded to a carbon atom which in turn is doubly bonded to another carbon atom
organic compound - any compound of carbon and another element or a radical
Based on WordNet 3.0, Farlex clipart collection. © 2003-2012 Princeton University, Farlex Inc.
References in periodicals archive ?
Heaton et al., "Palladium(II)/[beta]-diketonate complexes containing the enolates of N-acetyl-3-acyltetramic acids: crystal structure of the Lewis base adduct, [Pd(py)4](abta)2," Inorganica Chimica Acta, vol.
Negative results obtained under the same aqueous conditions with other reactive electrophiles (see supporting information), including electrophiles known to give products in reaction with tropinone enolates (e.g., cyanoformate and chloroformates [19, 34]), suggest that aldehydes are privileged reagents in this context.
After a general introduction and glossary, they cover practical aspects of asymmetric synthesis; enolate azaenolate, and organolithium alkylations; 1,2-additions and 1,4-additions to C=X bonds; aldol and Micheal additions of allyls, enolates, and enolate equivalents; cycloadditions and rearrangements; reductions and hydroborations, and oxidations.