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The reaction converts alkenes to dialkyl or aryl-alkyl ethers: Similarly, alkynes are converted to [[Vinyl group|vinyl]] ethers: ...

...perties while having higher boiling points than the lower-molecular-weight ethers and [[Alcohol (chemistry)|alcohol]]s. ...ethers and glycol ether acetates.{{cn|date=November 2022}} P-series glycol ethers are marketed as having lower toxicity than the E-series. ...

...oups. It is a colorless, [[flammable liquid]] with a sweet odor typical of ethers. ...ulfonic acid]] (a strong acid) and heat, in the same way other symmetrical ethers may be formed.<ref name="merck">{{Cite book| title = Merck Index of Chemica ...

...of theoretical interest as the simplest member of the class of di-tertiary ethers. [[Category:Dialkyl ethers]] ...

[[Category:Dialkyl ethers]] [[Category:Symmetrical ethers]] ...

...esson's reagent are created by the reaction of {{chem2|P4S10}} with aryl [[ethers]] which are different from [[anisole]]. For instance butoxybenzene and 2-te ...007}} that the reaction of 1,3,2,4-dithiadiphosphetane 2,4-disulfides with dialkyl cyanamides formed plant protection agents which contained six-membered ({{c ...

...t4=Heitmann|first5=Günther |last5=Strehlke|first6Dieter |last6=Mayer|title=Ethers, Aliphatic|year=2010|doi=10.1002/14356007.a10_023.pub2}}</ref> Diisopropyl [[Category:Dialkyl ethers]] ...

...ipidweb_html/lipids/complex/ethers/index.htm|title=Ether lipids - glyceryl ethers, plasmalogens, aldehydes, structure, biochemistry, composition and analysis Monoalkylglycerol ethers (MAGEs) are also generated from 2-acetyl MAGEs (precursors of PAF) by [[KIA ...

[[Category:Dialkyl ethers]] ...

...|first5=Jan A. J.|date=2000|title=Newly discovered non-isoprenoid glycerol dialkyl glycerol tetraether lipids in sediments|url=http://xlink.rsc.org/?DOI=b0045 ...amsté|first7=Jaap S.|date=2007-10-01|title=Archaeal and Bacterial Glycerol Dialkyl Glycerol Tetraether Lipids in Hot Springs of Yellowstone National Park|url= ...

...ergo head-to-head linkage to form [[caldarchaeol]] (one typical [[glycerol dialkyl glycerol tetraether]], GDGT), one of the most common tetraether lipid in ar ...rst5=Muriel|last6=Cravo-Laureau|first6=Cristiana|date=2015|title=Mono- and Dialkyl Glycerol Ether Lipids in Anaerobic Bacteria: Biosynthetic Insights from the ...

Unlike other alkyl ethers, dimethyl ether resists [[autoxidation]].<ref>''A comparative study on the [[Category:Dialkyl ethers]] ...

...=Konrad |date=1978 |title=Electrophilic Amination of "Carbanions" with N,N-Dialkyl-O-arylsulfonylhydroxylamines |journal=Angew. Chem. Int. Ed. Engl. |volume=1 ...doi=10.1002/anie.198300340 |issn=0570-0833}}</ref> Enolates and silyl enol ethers, the most widely used class of carbon nucleophiles in electrophilic aminati ...

...r not. Both aliphatic or aromatic substituents are known, they are called dialkyl or diaryl carbonates, respectively. The simplest members of these classes a ...

...someric homoallylsilanes, analogous to the mixture of products seen in the dialkyl case, or other insertion products (i.e. cyclopropanes). See [[beta-silicon This methodology has also been extended to heteroatom nucleophiles to produce ethers and thioethers.<ref>{{cite journal|last1=Zhihui|first1=S.|title=N-Tosylhydr ...

...a carbonyl group, reactions with particularly inexpensive urea and with [[dialkyl carbonate]]s such as [[dimethyl carbonate]] DMC and [[ethylene carbonate]] Most frequently, transesterifications of dialkyl carbonates, predominantly of [[dimethyl carbonate]], with acidic<ref>{{Cite ...

Another reaction that can be used for the preparation of ethers is the [[Williamson ether synthesis]], in which an [[alkoxide]] (produced b | title =Ethers, by Lawrence Karas and W. J. Piel ...

...e reaction]].<ref>{{cite journal|title=Sulfide Synthesis In Preparation Of Dialkyl And Alkyl Aryl Sulfides: Neopentyl Phenyl Sulfide|author1=D. Landini |autho ...

[[File:Thermo synth.png|center|thumb|446x446px|Thermolysis of dialkyl or diaryl-2-biphenylboranes to yield 9-borafluorene. (R = Et, ⁿP ...öster and Benedikt, who performed [[Thermal decomposition|thermolysis]] of dialkyl- or diaryl-2-biphenylboranes to release an alkane and yield the 9-borafluor ...

...it is used to drive the [[Schlenk equilibrium]], allowing the synthesis of dialkyl magnesium compounds.<ref name=Ullmann /> [[Dimethylmagnesium]] is prepared Like some other ethers, dioxane combines with atmospheric oxygen upon prolonged exposure to air to ...