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・ Trimethylolpropane
・ Trimethylolpropane phosphite
・ Trimethyloxonium tetrafluoroborate
・ Trimethylpentane
・ Trimethylphosphine
・ Trimethylsilane
・ Trimethylsilanol
・ Trimethylsilyl
・ Trimethylsilyl azide
・ Trimethylsilyl chloride
・ Trimethylsilyl cyanide
・ Trimethylsilyl cyclopentadiene
・ Trimethylsilyl iodide
・ Trimethylsilyl propanoic acid
・ Trimethylsilyl trifluoromethanesulfonate
Trimethylsilylacetylene
・ Trimethylsilyldiazomethane
・ Trimethylstibine
・ Trimethylsulfonium
・ Trimethylsulfonium—tetrahydrofolate N-methyltransferase
・ Trimethylsulfoxonium iodide
・ Trimethyltin chloride
・ Trimethyltryptamine
・ Trimethyluric acid
・ Trimeticcia di Segezia
・ Trimetopia
・ Trimetopon
・ Trimetopon barbouri
・ Trimetozine
・ Trimetrexate


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Trimethylsilylacetylene : ウィキペディア英語版
Trimethylsilylacetylene

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Trimethylsilylacetylene is an acetylene molecule protected on one end by the trimethylsilyl group. It is popularly used in alkynylations, e.g. the Sonogashira reaction. After desilylation (e.g. with TBAF), the ethynyl group is introduced. Using a protected alkyne, as opposed to acetylene gas, prevents further (undesired) coupling reactions and also has the benefit of being a liquid.
This compound is commercially available. It may also be prepared in a manner similar to other silyl compounds: deprotonation of acetylene with a Grignard reagent, followed by reaction with trimethylsilyl chloride.
==References==


抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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