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Enol
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===Deprotonation: enolates=== {{main|enolate}} Deprotonation of enolizable ketones, aldehydes, and esters gives [[enolate]]s.<ref>{{March6th}}</ref><ref name=enolate>{{cite book|title=Modern Enolate Chemistry: From Preparation to Applications in Asymmetric Synthesis|author=Manfred Braun|year=2015|isbn=9783527671069 |doi=10.1002/9783527671069 |publisher=Wiley-VCH}}</ref> Enolates can be trapped by the addition of electrophiles at oxygen. Silylation gives [[silyl enol ether]].<ref>Mukaiyama, T.; Kobayashi, S. ''[[Org. React.]]'' '''1994''', ''46'', 1. {{doi|10.1002/0471264180.or046.01}}</ref> Acylation gives esters such as [[vinyl acetate]].<ref name=Ullmann>{{cite encyclopedia|author=G. Roscher|title=Vinyl Esters|encyclopedia=Ullmann's Encyclopedia of Chemical Technology|year=2007|publisher=Wiley-VCH|location=Weinheim|doi=10.1002/14356007.a27_419|isbn=978-3527306732|s2cid=241676899 }}</ref>
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