Examples of 'dimethylsulfide' in a sentence
Meaning of "dimethylsulfide"
A volatile organic compound with a garlic-like odor, often found in marine environments and used as a chemical signal by certain organisms (dimethylsulfide)
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- Alternative spelling of dimethyl sulfide
How to use "dimethylsulfide" in a sentence
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dimethylsulfide
Starting from a mixture of dimethylsulfide and dimethylsulfate.
Dimethylsulfide in such cases acts as organic solvent.
The excess of peroxide was destroyed by addition of dimethylsulfide.
Several drops of dimethylsulfide were added followed by ethyl acetate.
In some embodiments the reducing agent is borane dimethylsulfide.
The dimethylsulfide is usually used in excess.
Oxidation may then be quenched by adding dimethylsulfide or potassium bisulfite.
A mixture of dimethylsulfide and dimethylsulfate with sodium hydroxide in dimethylsulfoxide.
Oxidation may optionally be quenched by adding dimethylsulfide or potassium bisulfite.
Dimethylsulfide causes the sulfuration of nickel and molybdenum oxides.
The reactants are typically contacted in an appropriate organic solvent such as dimethylsulfide.
Dimethylsulfide and anisole were included in all of the hydrogen fluoride cleavage solutions.
The reagent can be prepared by adding dimethylsulfate to water and dimethylsulfide.
In the case of dimethylsulfoxide, dimethylsulfide having foul is generated.
The mixture was warmed to ambient temperatures and quenched with excess dimethylsulfide.
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According to this document, dimethylsulfide is used in excess as organic solvent.
Generally preferred for its ease of use is borane dimethylsulfide complex.
For peptides containing methionine, dimethylsulfide and ethanedithiol were used as scavengers.
The sulfides are prepared by reduction of the amides with borane dimethylsulfide complexe.
Borane dimethylsulfide which is more stable than borane-tetrahydrofuran may also be used.
The flask was fitted with a distillation apparatus and the dimethylsulfide was removed.
Borane complexes, such as a borane dimethylsulfide complex, are especially useful in this reduction reaction.
The most preferred alkylsulfide and dialkylsulfide compounds are respectively dimethylsulfide and dimethyl disulfide.
In addition, the dimethylsulfide formed as a side product during the oxidation is not environmentally acceptable.
The solution was gassed with argon and quenched with dimethylsulfide dissolved in methanol.
Herein, Dimethylsulfide or ethanedithiol is preferably added to the anisole.
Best results are obtained using borane dimethylsulfide in THF.
However, malodorous dimethylsulfide is formed as a by-product of the reaction.
Additionally, the described process uses malodorous dimethylsulfide as a reagent.
Quench with dimethylsulfide ( 4 mL ) and stir overnight at room temperature.
The reagent of formula IV is formed from dimethylsulfide and dimethylsulfate.
In some embodiments, the stoichiometric oxidant is prepared in situ using N-chlorosuccinimide and dimethylsulfide.
The resulting ozonide and excess ozone are reduced by dimethylsulfide to produce compounds of formula 12.
The solution is purged with oxygen and argon, and then charged with 40 mL of dimethylsulfide.
Temporal and spatial distribution of dimethylsulfide in the subarctic Northeast Pacific Ocean,.
It all starts when tiny plankton in the oceans give off a gas called dimethylsulfide ( DMS ).
According to one alternative, dimethylsulfide is also used as solvent in step ( i ).
The method of claim 1, wherein said sulfur compound is dimethylsulfide.
The organic layer was treated with dimethylsulfide ( 10 µL ) and repeated the buffer wash.
In one embodiment, the reducing reagent is NaBH4, or borane dimethylsulfide.
Such examples include a dimethylsulfide complex, a triphenylphosphine complex, a trimethylphosphine complex, a tetrahydrofuran complex, and the like.
Additionally N-chlorosuccinimide and dimethylsulfide may be employed.
Formation of dimethylsulfide ( DMS ) by tissues after death is documented.
In general, the reagent of formula IV can be prepared from dimethylsulfide and dimethylsulfate.
Dimethylsulfide ( 3 ml ) was slowly added with stirring over a period of about 5 minutes.
To the refluxing solution is added about 1.1 equivalents of borane dimethylsulfide vía syringe.
The rotational spectrum of dimethylsulfide has been measured in the millimetre-wave range between 140 and 300 GHz.
To the refluxing solution is added 1,1 equivalents of a borane reagent, such as borane dimethylsulfide complex.
Preferably, the reduction is accomplished using borane dimethylsulfide complex in THF at about 60°C.
The organic layer was separated and repeated again the buffer wash after adding dimethylsulfide ( 15 mL ).
