http://wiki.sbeccompany.fr/ws/index.php?action=history&feed=atom&title=Abr%C3%A9viations_courantes_en_chimie_organique Abréviations courantes en chimie organique - Historique des versions 2026-05-05T12:19:43Z Historique des révisions pour cette page sur le wiki MediaWiki 1.36.1 http://wiki.sbeccompany.fr/ws/index.php?title=Abr%C3%A9viations_courantes_en_chimie_organique&diff=15&oldid=prev Sébastien Bruneau : Page créée avec « __NOTOC__ {{up}}Accueil | Chimie | Document | Abbréviations courantes en chimie organique ---- ==A== {|border="0" cellpaddin… » 2021-08-09T17:08:06Z <p>Page créée avec « __NOTOC__ {{up}}<a href="/ws/index.php?title=Accueil" class="mw-redirect" title="Accueil">Accueil</a> | <a href="/ws/index.php?title=Chimie" title="Chimie">Chimie</a> | <a href="/ws/index.php?title=Documents_relatifs_%C3%A0_la_chimie" title="Documents relatifs à la chimie">Document</a> | Abbréviations courantes en chimie organique ---- ==A== {|border=&quot;0&quot; cellpaddin… »</p> <p><b>Nouvelle page</b></p><div>__NOTOC__<br /> {{up}}[[Accueil]] | [[Chimie]] | [[Documents relatifs à la chimie|Document]] | Abbréviations courantes en chimie organique<br /> <br /> ----<br /> <br /> ==A==<br /> {|border=&quot;0&quot; cellpadding=&quot;2&quot; width=&quot;100%&quot;<br /> |-<br /> |bgcolor=#DDEAEE align=&quot;center&quot; width=&quot;20%&quot;|Abbréviation ou sigle<br /> |bgcolor=#DDE4EE align=&quot;center&quot; width=&quot;35%&quot;|Nom courant<br /> |bgcolor=#DDDDEE align=&quot;center&quot; width=&quot;55%&quot;|Nom IUPAC / Nomenclature systématique<br /> |-<br /> |bgcolor=#EEFAFF align=&quot;center&quot; |[[:Image:acetyl.jpg|Ac]]<br /> |bgcolor=#EEF4FF align=&quot;center&quot; |acétyle&lt;br&gt;&#039;&#039;acetyl&#039;&#039;<br /> |bgcolor=#EEEEFF align=&quot;center&quot; |acétyle&lt;br&gt;&#039;&#039;acetyl&#039;&#039;<br /> |-<br /> |bgcolor=#EEFAFF align=&quot;center&quot; |AIBN<br /> |bgcolor=#EEF4FF align=&quot;center&quot; |azoisobutyronitrile&lt;br&gt;&#039;&#039;azoisobutyronitrile&#039;&#039;<br /> |bgcolor=#EEEEFF align=&quot;center&quot; |azobis(isobutyronitrile)&lt;br&gt;&#039;&#039;azobis(isobutyronitrile)&#039;&#039;<br /> |-<br /> |bgcolor=#EEFAFF align=&quot;center&quot; |[[:Image:APTS.jpg|APTS]] ou TsOH<br /> |bgcolor=#EEF4FF align=&quot;center&quot; |acide &#039;&#039;para&#039;&#039;-toluènesufonique&lt;br&gt;para-&#039;&#039;toluenesufonic acid&#039;&#039;<br /> |bgcolor=#EEEEFF align=&quot;center&quot; |acide 4-méthylphénylsulfonique&lt;br&gt;&#039;&#039;4-methylphenylsulfonique acid&#039;&#039;<br /> |-<br /> |bgcolor=#EEFAFF align=&quot;center&quot; |Ar<br /> |bgcolor=#EEF4FF align=&quot;center&quot; |aryle&lt;br&gt;&#039;&#039;aryl&#039;&#039;<br /> |bgcolor=#EEEEFF align=&quot;center&quot; |(substituant aromatique)&lt;br&gt;&#039;&#039;(aromatic substituant)&#039;&#039;<br /> |-<br /> |}<br /> <br /> ==B==<br /> {|border=&quot;0&quot; cellpadding=&quot;2&quot; width=&quot;100%&quot;<br /> |-<br /> |bgcolor=#DDEAEE align=&quot;center&quot; width=&quot;20%&quot;|Abbréviation ou sigle<br /> |bgcolor=#DDE4EE align=&quot;center&quot; width=&quot;35%&quot;|Nom courant<br /> |bgcolor=#DDDDEE align=&quot;center&quot; width=&quot;55%&quot;|Nom IUPAC / Nomenclature systématique<br /> |-<br /> |bgcolor=#EEFAFF align=&quot;center&quot; |[[:Image:Benzyle.jpg|Bn]]<br /> |bgcolor=#EEF4FF align=&quot;center&quot; |benzyle&lt;br&gt;&#039;&#039;benzyl&#039;&#039;<br /> |bgcolor=#EEEEFF align=&quot;center&quot; |benzyle&lt;br&gt;&#039;&#039;benzyl&#039;&#039;<br /> |-<br /> |bgcolor=#EEFAFF align=&quot;center&quot; |[[:Image:Boc.png|Boc]]<br /> |bgcolor=#EEF4FF align=&quot;center&quot; |tert-butyloxycarbonyle&lt;br&gt;&#039;&#039;tert-butyloxycarbonyle&#039;&#039;<br /> |bgcolor=#EEEEFF align=&quot;center&quot; |1,1-diméthyléthoxycarbonyle&lt;br&gt;&#039;&#039;1,1-dimethylethoxycarbonyle&#039;&#039;<br /> |-<br /> |bgcolor=#EEFAFF align=&quot;center&quot; |Bs<br /> |bgcolor=#EEF4FF align=&quot;center&quot; |brosyle&lt;br&gt;&#039;&#039;brosyl&#039;&#039;<br /> |bgcolor=#EEEEFF align=&quot;center&quot; |&#039;&#039;p&#039;&#039;-bromobenzènesulfonyle&lt;br&gt;p&#039;&#039;-bromobenzenesulfonyle&#039;&#039;<br /> |-<br /> |bgcolor=#EEFAFF align=&quot;center&quot; |Bu<br /> |bgcolor=#EEF4FF align=&quot;center&quot; |butyle&lt;br&gt;&#039;&#039;butyl&#039;&#039;<br /> |bgcolor=#EEEEFF align=&quot;center&quot; |butyle&lt;br&gt;&#039;&#039;butyl&#039;&#039;<br /> |-<br /> |bgcolor=#EEFAFF align=&quot;center&quot; |[[:Image:benzoyle.jpg|Bz]]<br /> |bgcolor=#EEF4FF align=&quot;center&quot; |benzoyle&lt;br&gt;&#039;&#039;benzoyl&#039;&#039;<br /> |bgcolor=#EEEEFF align=&quot;center&quot; |benzoyle&lt;br&gt;&#039;&#039;benzoyl&#039;&#039;<br /> |-<br /> |}<br /> <br /> ==C==<br /> {|border=&quot;0&quot; cellpadding=&quot;2&quot; width=&quot;100%&quot;<br /> |-<br /> |bgcolor=#DDEAEE align=&quot;center&quot; width=&quot;20%&quot;|Abbréviation ou sigle<br /> |bgcolor=#DDE4EE align=&quot;center&quot; width=&quot;35%&quot;|Nom courant<br /> |bgcolor=#DDDDEE align=&quot;center&quot; width=&quot;55%&quot;|Nom IUPAC / Nomenclature systématique<br /> |-<br /> |bgcolor=#EEFAFF align=&quot;center&quot; |[[:Image:cyclopentanedienyl.jpg|Cp]]<br /> |bgcolor=#EEF4FF align=&quot;center&quot; |cyclopentanediènyle&lt;br&gt;&#039;&#039;cyclopentanedienyl&#039;&#039;<br /> |bgcolor=#EEEEFF align=&quot;center&quot; |cyclopentanediènyle&lt;br&gt;&#039;&#039;cyclopentanedienyl&#039;&#039;<br /> |-<br /> |bgcolor=#EEFAFF align=&quot;center&quot; |[[:Image:cyclohexyle.jpg|Cy]]<br /> |bgcolor=#EEF4FF align=&quot;center&quot; |cyclohexyle&lt;br&gt;&#039;&#039;cyclohexyl&#039;&#039;<br /> |bgcolor=#EEEEFF align=&quot;center&quot; |cyclohexyle&lt;br&gt;&#039;&#039;cyclohexyl&#039;&#039;<br /> |-<br /> |}<br /> <br /> ==D==<br /> {|border=&quot;0&quot; cellpadding=&quot;2&quot; width=&quot;100%&quot;<br /> |-<br /> |bgcolor=#DDEAEE align=&quot;center&quot; width=&quot;20%&quot;|Abbréviation ou sigle<br /> |bgcolor=#DDE4EE align=&quot;center&quot; width=&quot;35%&quot;|Nom courant<br /> |bgcolor=#DDDDEE align=&quot;center&quot; width=&quot;55%&quot;|Nom IUPAC / Nomenclature systématique<br /> |-<br /> |bgcolor=#EEFAFF align=&quot;center&quot; |[[:Image:dcc.jpg|DCC]]<br /> |bgcolor=#EEF4FF align=&quot;center&quot; |N,N&#039;-dicyclohexylcarbodiimide&lt;br&gt;&#039;&#039;N,N&#039;-dicyclohexylcarbodiimide&#039;&#039;<br /> |bgcolor=#EEEEFF align=&quot;center&quot; |N,N&#039;-dicyclohexylcarbodiimide&lt;br&gt;&#039;&#039;N,N&#039;-dicyclohexylcarbodiimide&#039;&#039;<br /> |-<br /> |bgcolor=#EEFAFF align=&quot;center&quot; |DCM<br /> |bgcolor=#EEF4FF align=&quot;center&quot; |dichlorométhane&lt;br&gt;&#039;&#039;dichloromethane&#039;&#039;<br /> |bgcolor=#EEEEFF align=&quot;center&quot; |dichlorométhane&lt;br&gt;&#039;&#039;dichloromethane&#039;&#039;<br /> |-<br /> |bgcolor=#EEFAFF align=&quot;center&quot; |[[:Image:dcu.jpg|DCU]]<br /> |bgcolor=#EEF4FF align=&quot;center&quot; |dicyclohexylurée&lt;br&gt;&#039;&#039;dicyclohexylurea&#039;&#039;<br /> |bgcolor=#EEEEFF align=&quot;center&quot; |bis(cyclohexylamino)méthanal&lt;br&gt;&#039;&#039;bis(cyclohexylamino)methanal&#039;&#039;<br /> |-<br /> |bgcolor=#EEFAFF align=&quot;center&quot; |[[:Image:dhf.jpg|DHF]]<br /> |bgcolor=#EEF4FF align=&quot;center&quot; |dihydrofurane&lt;br&gt;&#039;&#039;dihydrofuran&#039;&#039;<br /> |bgcolor=#EEEEFF align=&quot;center&quot; |dihydrofurane&lt;br&gt;&#039;&#039;dihydrofuran&#039;&#039;<br /> |-<br /> |bgcolor=#EEFAFF align=&quot;center&quot; |[[:Image:oxane.jpg|DHP]]<br /> |bgcolor=#EEF4FF align=&quot;center&quot; |dihydropyrane &#039;&#039;ou&#039;&#039; oxane&lt;br&gt;&#039;&#039;dihydropyran&#039;&#039; or &#039;&#039;oxane&#039;&#039;<br /> |bgcolor=#EEEEFF align=&quot;center&quot; |dihydropyrane&lt;br&gt;&#039;&#039;dihydropyran&#039;&#039;<br /> |-<br /> |bgcolor=#EEFAFF align=&quot;center&quot; |[[:Image:dmf.jpg|DMF]]<br /> |bgcolor=#EEF4FF align=&quot;center&quot; |diméthylformamide&lt;br&gt;&#039;&#039;dimethylformamide&#039;&#039;<br /> |bgcolor=#EEEEFF align=&quot;center&quot; |N,N-diméthylméthanamide&lt;br&gt;&#039;&#039;N,N-dimethylmethanamide&#039;&#039;<br /> |-<br /> |bgcolor=#EEFAFF align=&quot;center&quot; |[[:Image:dmap.png|DMAP]]<br /> |bgcolor=#EEF4FF align=&quot;center&quot; |4-Diméthylaminopyridine&lt;br&gt;&#039;&#039;4-Dimethylaminopyridine&#039;&#039;<br /> |bgcolor=#EEEEFF align=&quot;center&quot; |4-(Diméthylamino)azabenzène&lt;br&gt;&#039;&#039;4-(Dimethylamino)azabenzene&#039;&#039;<br /> |-<br /> |bgcolor=#EEFAFF align=&quot;center&quot; |[[:Image:dmso.jpg|DMSO]]<br /> |bgcolor=#EEF4FF align=&quot;center&quot; |diméthylsulfoxyde&lt;br&gt;&#039;&#039;dimethylsulfoxide&#039;&#039;<br /> |bgcolor=#EEEEFF align=&quot;center&quot; |diméthylsulfoxyde&lt;br&gt;&#039;&#039;dimethylsulfoxide&#039;&#039;<br /> |-<br /> |}<br /> <br /> ==E==<br /> {|border=&quot;0&quot; cellpadding=&quot;2&quot; width=&quot;100%&quot;<br /> |-<br /> |bgcolor=#DDEAEE align=&quot;center&quot; width=&quot;20%&quot;|Abbréviation ou sigle<br /> |bgcolor=#DDE4EE align=&quot;center&quot; width=&quot;35%&quot;|Nom courant<br /> |bgcolor=#DDDDEE align=&quot;center&quot; width=&quot;55%&quot;|Nom IUPAC / Nomenclature systématique<br /> |-<br /> |bgcolor=#EEFAFF align=&quot;center&quot; |Et<br /> |bgcolor=#EEF4FF align=&quot;center&quot; |éthyle&lt;br&gt;&#039;&#039;ethyl&#039;&#039;<br /> |bgcolor=#EEEEFF align=&quot;center&quot; |éthyle&lt;br&gt;&#039;&#039;ethyl&#039;&#039;<br /> |-<br /> |}<br /> <br /> ==F==<br /> {|border=&quot;0&quot; cellpadding=&quot;2&quot; width=&quot;100%&quot;<br /> |-<br /> |bgcolor=#DDEAEE align=&quot;center&quot; width=&quot;20%&quot;|Abbréviation ou sigle<br /> |bgcolor=#DDE4EE align=&quot;center&quot; width=&quot;35%&quot;|Nom courant<br /> |bgcolor=#DDDDEE align=&quot;center&quot; width=&quot;55%&quot;|Nom IUPAC / Nomenclature systématique<br /> |-<br /> |bgcolor=#EEFAFF align=&quot;center&quot; |[[:Image:fmoc.jpg|fmoc]]<br /> |bgcolor=#EEF4FF align=&quot;center&quot; |9-fluorénylméthoxycarbonyle&lt;br&gt;&#039;&#039;9-fluorenylmethoxycarbonyl&#039;&#039;<br /> |bgcolor=#EEEEFF align=&quot;center&quot; |9-fluorénylméthoxycarbonyle&lt;br&gt;&#039;&#039;9-fluorenylmethoxycarbonyl&#039;&#039;<br /> |-<br /> |}<br /> <br /> ==H==<br /> {|border=&quot;0&quot; cellpadding=&quot;2&quot; width=&quot;100%&quot;<br /> |-<br /> |bgcolor=#DDEAEE align=&quot;center&quot; width=&quot;20%&quot;|Abbréviation ou sigle<br /> |bgcolor=#DDE4EE align=&quot;center&quot; width=&quot;35%&quot;|Nom courant<br /> |bgcolor=#DDDDEE align=&quot;center&quot; width=&quot;55%&quot;|Nom IUPAC / Nomenclature systématique<br /> |-<br /> |bgcolor=#EEFAFF align=&quot;center&quot; |Hex<br /> |bgcolor=#EEF4FF align=&quot;center&quot; |hexyle&lt;br&gt;&#039;&#039;hexyl&#039;&#039;<br /> |bgcolor=#EEEEFF align=&quot;center&quot; |hexyle&lt;br&gt;&#039;&#039;hexyl&#039;&#039;<br /> |-<br /> |}<br /> <br /> ==I==<br /> {|border=&quot;0&quot; cellpadding=&quot;2&quot; width=&quot;100%&quot;<br /> |-<br /> |bgcolor=#DDEAEE align=&quot;center&quot; width=&quot;20%&quot;|Abbréviation ou sigle<br /> |bgcolor=#DDE4EE align=&quot;center&quot; width=&quot;35%&quot;|Nom courant<br /> |bgcolor=#DDDDEE align=&quot;center&quot; width=&quot;55%&quot;|Nom IUPAC / Nomenclature systématique<br /> |-<br /> |bgcolor=#EEFAFF align=&quot;center&quot; |&lt;sup&gt;i&lt;/sup&gt;Bu<br /> |bgcolor=#EEF4FF align=&quot;center&quot; |isobutyle&lt;br&gt;&#039;&#039;isobutyl&#039;&#039;<br /> |bgcolor=#EEEEFF align=&quot;center&quot; |2-méthylpropyle&lt;br&gt;&#039;&#039;2-methylpropyl&#039;&#039;<br /> |-<br /> |bgcolor=#EEFAFF align=&quot;center&quot; |[[:Image:ipr.jpg|&lt;sup&gt;i&lt;/sup&gt;Pr]]<br /> |bgcolor=#EEF4FF align=&quot;center&quot; |isopropyle&lt;br&gt;&#039;&#039;isopropyl&#039;&#039;<br /> |bgcolor=#EEEEFF align=&quot;center&quot; |méthyléthyle&lt;br&gt;&#039;&#039;methylethyl&#039;&#039;<br /> |-<br /> |}<br /> <br /> ==L==<br /> {|border=&quot;0&quot; cellpadding=&quot;2&quot; width=&quot;100%&quot;<br /> |-<br /> |bgcolor=#DDEAEE align=&quot;center&quot; width=&quot;20%&quot;|Abbréviation ou sigle<br /> |bgcolor=#DDE4EE align=&quot;center&quot; width=&quot;35%&quot;|Nom courant<br /> |bgcolor=#DDDDEE align=&quot;center&quot; width=&quot;55%&quot;|Nom IUPAC / Nomenclature systématique<br /> |-<br /> |bgcolor=#EEFAFF align=&quot;center&quot; |[[:Image:lda.jpg|LDA]]<br /> |bgcolor=#EEF4FF align=&quot;center&quot; |diisopropylamidure de lithium&lt;br&gt;&#039;&#039;lithium diisopropylamide&#039;&#039;<br /> |bgcolor=#EEEEFF align=&quot;center&quot; |diisopropylamidure de lithium&lt;br&gt;&#039;&#039;lithium diisopropylamide&#039;&#039;<br /> |-<br /> |bgcolor=#EEFAFF align=&quot;center&quot; |[[:Image:lev.jpg|Lev]]<br /> |bgcolor=#EEF4FF align=&quot;center&quot; |lévulinyle&lt;br&gt;&#039;&#039;levulinyle&#039;&#039;<br /> |bgcolor=#EEEEFF align=&quot;center&quot; |4-oxopentanoyle&lt;br&gt;&#039;&#039;4-oxopentanoyle&#039;&#039;<br /> |-<br /> |}<br /> <br /> ==M==<br /> {|border=&quot;0&quot; cellpadding=&quot;2&quot; width=&quot;100%&quot;<br /> |-<br /> |bgcolor=#DDEAEE align=&quot;center&quot; width=&quot;20%&quot;|Abbréviation ou sigle<br /> |bgcolor=#DDE4EE align=&quot;center&quot; width=&quot;35%&quot;|Nom courant<br /> |bgcolor=#DDDDEE align=&quot;center&quot; width=&quot;55%&quot;|Nom IUPAC / Nomenclature systématique<br /> |-<br /> |bgcolor=#EEFAFF align=&quot;center&quot; |[[:Image:mcpba.jpg|mCpBA]]<br /> |bgcolor=#EEF4FF align=&quot;center&quot; |acide méta-chloroperbenzoïque&lt;br&gt;&#039;&#039;meta-chloroperbenzoic&#039;&#039;<br /> |bgcolor=#EEEEFF align=&quot;center&quot; |acide 3-chloroperoxybenzoïque&lt;br&gt;&#039;&#039;3-chloroperoxybenzoic acid&#039;&#039;<br /> |-<br /> |bgcolor=#EEFAFF align=&quot;center&quot; |Me<br /> |bgcolor=#EEF4FF align=&quot;center&quot; |méthyle&lt;br&gt;&#039;&#039;methyl&#039;&#039;<br /> |bgcolor=#EEEEFF align=&quot;center&quot; |méthyle&lt;br&gt;&#039;&#039;methyl&#039;&#039;<br /> |-<br /> |bgcolor=#EEFAFF align=&quot;center&quot; |[[:Image:mem.jpg|MEM]]<br /> |bgcolor=#EEF4FF align=&quot;center&quot; |2-méthoxyéthoxyméthyle&lt;br&gt;&#039;&#039;2-methoxyethoxymethyl&#039;&#039;<br /> |bgcolor=#EEEEFF align=&quot;center&quot; |2-méthoxyéthoxyméthyle&lt;br&gt;&#039;&#039;2-methoxyethoxymethyl&#039;&#039;<br /> |-<br /> |bgcolor=#EEFAFF align=&quot;center&quot; |Mes<br /> |bgcolor=#EEF4FF align=&quot;center&quot; |mésityle&lt;br&gt;&#039;&#039;mesityl&#039;&#039;<br /> |bgcolor=#EEEEFF align=&quot;center&quot; |2,4,6-triméthylphényle&lt;br&gt;&#039;&#039;2,4,6-trimethylphenyl&#039;&#039;<br /> |-<br /> |bgcolor=#EEFAFF align=&quot;center&quot; |[[:Image:mom.jpg|MOM]]<br /> |bgcolor=#EEF4FF align=&quot;center&quot; |méthoxyméthyle&lt;br&gt;&#039;&#039;methoxymethyl&#039;&#039;<br /> |bgcolor=#EEEEFF align=&quot;center&quot; |méthoxyméthyle&lt;br&gt;&#039;&#039;methoxymethyl&#039;&#039;<br /> |-<br /> |bgcolor=#EEFAFF align=&quot;center&quot; |[[:Image:mesyle.jpg|Ms]]<br /> |bgcolor=#EEF4FF align=&quot;center&quot; |mésyle&lt;br&gt;&#039;&#039;mesyl&#039;&#039;<br /> |bgcolor=#EEEEFF align=&quot;center&quot; |méthylsulfonyle&lt;br&gt;&#039;&#039;methylsulfonyl&#039;&#039;<br /> |-<br /> |}<br /> <br /> ==N==<br /> {|border=&quot;0&quot; cellpadding=&quot;2&quot; width=&quot;100%&quot;<br /> |-<br /> |bgcolor=#DDEAEE align=&quot;center&quot; width=&quot;20%&quot;|Abbréviation ou sigle<br /> |bgcolor=#DDE4EE align=&quot;center&quot; width=&quot;35%&quot;|Nom courant<br /> |bgcolor=#DDDDEE align=&quot;center&quot; width=&quot;55%&quot;|Nom IUPAC / Nomenclature systématique<br /> |-<br /> |bgcolor=#EEFAFF align=&quot;center&quot; |NBS<br /> |bgcolor=#EEF4FF align=&quot;center&quot; |N-Bromosuccinimide&lt;br&gt;&#039;&#039;N-Bromosuccinimide&#039;&#039;<br /> |bgcolor=#EEEEFF align=&quot;center&quot; |1-bromo-2,5-pyrolidinedione&lt;br&gt;&#039;&#039;1-Bromo-2,5-pyrolidinedione&#039;&#039;<br /> |-<br /> |}<br /> <br /> ==P==<br /> {|border=&quot;0&quot; cellpadding=&quot;2&quot; width=&quot;100%&quot;<br /> |-<br /> |bgcolor=#DDEAEE align=&quot;center&quot; width=&quot;20%&quot;|Abbréviation ou sigle<br /> |bgcolor=#DDE4EE align=&quot;center&quot; width=&quot;35%&quot;|Nom courant<br /> |bgcolor=#DDDDEE align=&quot;center&quot; width=&quot;55%&quot;|Nom IUPAC / Nomenclature systématique<br /> |-<br /> |bgcolor=#EEFAFF align=&quot;center&quot; |Ph &amp;nbsp;&amp;nbsp;ou&amp;nbsp;&amp;nbsp; &amp;phi;<br /> |bgcolor=#EEF4FF align=&quot;center&quot; |phenyle&lt;br&gt;&#039;&#039;phenyl&#039;&#039;<br /> |bgcolor=#EEEEFF align=&quot;center&quot; |phenyle&lt;br&gt;&#039;&#039;phenyl&#039;&#039;<br /> |-<br /> |bgcolor=#EEFAFF align=&quot;center&quot; |Piv<br /> |bgcolor=#EEF4FF align=&quot;center&quot; |pivaloyle&lt;br&gt;&#039;&#039;pivaloyl&#039;&#039;<br /> |bgcolor=#EEEEFF align=&quot;center&quot; |2,2-diméthylpropanoyle&lt;br&gt;&#039;&#039;2,2-dimethylpropanoyl&#039;&#039;<br /> |-<br /> |bgcolor=#EEFAFF align=&quot;center&quot; |PPTS &amp;nbsp;&amp;nbsp;ou&amp;nbsp;&amp;nbsp; TsO{{-}}PyH{{+}}<br /> |bgcolor=#EEF4FF align=&quot;center&quot; |tosylate de pyridinium&lt;br&gt;&#039;&#039;pyridinium tosylate&#039;&#039;<br /> |bgcolor=#EEEEFF align=&quot;center&quot; |&#039;&#039;para&#039;&#039;-toluènesulfonate de pyridinium&lt;br&gt;&#039;&#039;pyridinium&#039;&#039; para&#039;&#039;-toluenesulfonate&#039;&#039;<br /> |-<br /> |bgcolor=#EEFAFF align=&quot;center&quot; |Pr<br /> |bgcolor=#EEF4FF align=&quot;center&quot; |propyle&lt;br&gt;&#039;&#039;propyl&#039;&#039;<br /> |bgcolor=#EEEEFF align=&quot;center&quot; |propyle&lt;br&gt;&#039;&#039;propyl&#039;&#039;<br /> |-<br /> |bgcolor=#EEFAFF align=&quot;center&quot; |Py &amp;nbsp;&amp;nbsp;ou&amp;nbsp;&amp;nbsp; &amp;pi;<br /> |bgcolor=#EEF4FF align=&quot;center&quot; |pyridine&lt;br&gt;&#039;&#039;pyridine&#039;&#039;<br /> |bgcolor=#EEEEFF align=&quot;center&quot; |azabenzène&lt;br&gt;&#039;&#039;azabenzene&#039;&#039;<br /> |-<br /> |}<br /> <br /> ==S==<br /> {|border=&quot;0&quot; cellpadding=&quot;2&quot; width=&quot;100%&quot;<br /> |-<br /> |bgcolor=#DDEAEE align=&quot;center&quot; width=&quot;20%&quot;|Abbréviation ou sigle<br /> |bgcolor=#DDE4EE align=&quot;center&quot; width=&quot;35%&quot;|Nom courant<br /> |bgcolor=#DDDDEE align=&quot;center&quot; width=&quot;55%&quot;|Nom IUPAC / Nomenclature systématique<br /> |-<br /> |bgcolor=#EEFAFF align=&quot;center&quot; |&lt;sup&gt;s&lt;/sup&gt;Bu<br /> |bgcolor=#EEF4FF align=&quot;center&quot; |sec-butyle&lt;br&gt;&#039;&#039;sec-butyl&#039;&#039;<br /> |bgcolor=#EEEEFF align=&quot;center&quot; |1-méthylpropyle&lt;br&gt;&#039;&#039;1-methylpropyl&#039;&#039;<br /> |-<br /> |bgcolor=#EEFAFF align=&quot;center&quot; |SES<br /> |bgcolor=#EEF4FF align=&quot;center&quot; |2-(triméthylsilyl)éthanesulfonyle&lt;br&gt;&#039;&#039;2-(trimethylsilyl)ethanesulfonyl&#039;&#039;<br /> |bgcolor=#EEEEFF align=&quot;center&quot; |2-(triméthylsilyl)éthanesulfonyle&lt;br&gt;&#039;&#039;2-(trimethylsilyl)ethanesulfonyl&#039;&#039;<br /> |-<br /> |}<br /> <br /> ==T==<br /> {|border=&quot;0&quot; cellpadding=&quot;2&quot; width=&quot;100%&quot;<br /> |-<br /> |bgcolor=#DDEAEE align=&quot;center&quot; width=&quot;20%&quot;|Abbréviation ou sigle<br /> |bgcolor=#DDE4EE align=&quot;center&quot; width=&quot;35%&quot;|Nom courant<br /> |bgcolor=#DDDDEE align=&quot;center&quot; width=&quot;55%&quot;|Nom IUPAC / Nomenclature systématique<br /> |-<br /> |bgcolor=#EEFAFF align=&quot;center&quot; |TBAF<br /> |bgcolor=#EEF4FF align=&quot;center&quot; |fluorure de tétrabutylammonium&lt;br&gt;&#039;&#039;tetrabutylammonium fluoride&#039;&#039;<br /> |bgcolor=#EEEEFF align=&quot;center&quot; |fluorure de tétrabutylammonium&lt;br&gt;&#039;&#039;tetrabutylammonium fluoride&#039;&#039;<br /> |-<br /> |bgcolor=#EEFAFF align=&quot;center&quot; |TBDMS ou TBS<br /> |bgcolor=#EEF4FF align=&quot;center&quot; |tert-butyldiméthylsilyle&lt;br&gt;&#039;&#039;tert-butyldimethylsilyl&#039;&#039;<br /> |bgcolor=#EEEEFF align=&quot;center&quot; |tert-butyldiméthylsilyle&lt;br&gt;&#039;&#039;tert-butyldimethylsilyl&#039;&#039;<br /> |-<br /> |bgcolor=#EEFAFF align=&quot;center&quot; |TBDPS<br /> |bgcolor=#EEF4FF align=&quot;center&quot; |tert-butyldiphénylsilyle&lt;br&gt;&#039;&#039;tert-butyldiphenylsilyl&#039;&#039;<br /> |bgcolor=#EEEEFF align=&quot;center&quot; |tert-butyldiphénylsilyle&lt;br&gt;&#039;&#039;tert-butyldiphenylsilyl&#039;&#039;<br /> |-<br /> |bgcolor=#EEFAFF align=&quot;center&quot; |&lt;sup&gt;t&lt;/sup&gt;Bu<br /> |bgcolor=#EEF4FF align=&quot;center&quot; |tert-butyle&lt;br&gt;&#039;&#039;tert-butyl&#039;&#039;<br /> |bgcolor=#EEEEFF align=&quot;center&quot; |1,1-diméthyléthyle&lt;br&gt;&#039;&#039;1,1-dimethylethyle&#039;&#039;<br /> |-<br /> |bgcolor=#EEFAFF align=&quot;center&quot; |TES<br /> |bgcolor=#EEF4FF align=&quot;center&quot; |triéthylsilyle&lt;br&gt;&#039;&#039;triethylsilyl&#039;&#039;<br /> |bgcolor=#EEEEFF align=&quot;center&quot; |triéthylsilyle&lt;br&gt;&#039;&#039;triethylsilyl&#039;&#039;<br /> |-<br /> |bgcolor=#EEFAFF align=&quot;center&quot; |Tf<br /> |bgcolor=#EEF4FF align=&quot;center&quot; |triflyle&lt;br&gt;&#039;&#039;triflyl&#039;&#039;<br /> |bgcolor=#EEEEFF align=&quot;center&quot; |trifluorométhylsulfonyle&lt;br&gt;&#039;&#039;trifluoromethylsulfonyl&#039;&#039;<br /> |-<br /> |bgcolor=#EEFAFF align=&quot;center&quot; |TFAA<br /> |bgcolor=#EEF4FF align=&quot;center&quot; |acide trifluoroacétique&lt;br&gt;&#039;&#039;trifluoroacetic acid&#039;&#039;<br /> |bgcolor=#EEEEFF align=&quot;center&quot; |acide trifluoroéthanoïque&lt;br&gt;&#039;&#039;trifluoroethanoic acid&#039;&#039;<br /> |-<br /> |bgcolor=#EEFAFF align=&quot;center&quot; |[[:Image:Thf.png|THF]]<br /> |bgcolor=#EEF4FF align=&quot;center&quot; |tetrahydrofurane&lt;br&gt;&#039;&#039;tetrahydrofuran&#039;&#039;<br /> |bgcolor=#EEEEFF align=&quot;center&quot; |oxacyclopentane&lt;br&gt;&#039;&#039;oxacyclopentane&#039;&#039;<br /> |-<br /> |bgcolor=#EEFAFF align=&quot;center&quot; |THP<br /> |bgcolor=#EEF4FF align=&quot;center&quot; |tetrahydropyrane&lt;br&gt;&#039;&#039;tetrahydropyran&#039;&#039;<br /> |bgcolor=#EEEEFF align=&quot;center&quot; |oxacyclohexane&lt;br&gt;&#039;&#039;oxacyclohexane&#039;&#039;<br /> |-<br /> |bgcolor=#EEFAFF align=&quot;center&quot; |TMS<br /> |bgcolor=#EEF4FF align=&quot;center&quot; |tétraméthylsilane&lt;br&gt;&#039;&#039;tetramethylsilane&#039;&#039;<br /> |bgcolor=#EEEEFF align=&quot;center&quot; |tétraméthylsilane&lt;br&gt;&#039;&#039;tetramethylsilane&#039;&#039;<br /> |-<br /> |bgcolor=#EEFAFF align=&quot;center&quot; |TMS<br /> |bgcolor=#EEF4FF align=&quot;center&quot; |triméthylsilyle&lt;br&gt;&#039;&#039;trimethylsilyl&#039;&#039;<br /> |bgcolor=#EEEEFF align=&quot;center&quot; |triméthylsilyle&lt;br&gt;&#039;&#039;trimethylsilyl&#039;&#039;<br /> |-<br /> |bgcolor=#EEFAFF align=&quot;center&quot; |Tol<br /> |bgcolor=#EEF4FF align=&quot;center&quot; |toluène&lt;br&gt;&#039;&#039;toluène&#039;&#039;<br /> |bgcolor=#EEEEFF align=&quot;center&quot; |méthylbenzène&lt;br&gt;&#039;&#039;methylbenzene&#039;&#039;<br /> |-<br /> |bgcolor=#EEFAFF align=&quot;center&quot; |Tr<br /> |bgcolor=#EEF4FF align=&quot;center&quot; |trityle&lt;br&gt;&#039;&#039;trityl&#039;&#039;<br /> |bgcolor=#EEEEFF align=&quot;center&quot; |triphénylméthyle&lt;br&gt;&#039;&#039;triphenylmethyl&#039;&#039;<br /> |-<br /> |bgcolor=#EEFAFF align=&quot;center&quot; |Ts ou Tos<br /> |bgcolor=#EEF4FF align=&quot;center&quot; |tosyle&lt;br&gt;&#039;&#039;tosyl&#039;&#039;<br /> |bgcolor=#EEEEFF align=&quot;center&quot; |&#039;&#039;p&#039;&#039;-méthylbenzènesulfonyle&lt;br&gt;p&#039;&#039;-methylbenzenesulfonyle&#039;&#039;<br /> |-<br /> |}<br /> <br /> {{espace}}{{espace}}<br /> {{portail chimie}}<br /> <br /> [[Catégorie:Chimie]]</div> Sébastien Bruneau