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・ Trimethylolethane trinitrate
・ 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


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Trimethylsilyl trifluoromethanesulfonate : ウィキペディア英語版
Trimethylsilyl trifluoromethanesulfonate

Trimethylsilyl trifluoromethanesulfonate is a trifluoromethanesulfonate derivate with a trimethylsilyl R-group. It has similar reactivity to trimethylsilyl chloride, and is also used often in organic synthesis.
== Examples of use ==
The stereoselective synthesis of seven benzylated proanthocyanidin trimers (epicatechin-(4β-8)-epicatechin-(4β-8)-epicatechin trimer (procyanidin C1), catechin-(4α-8)-catechin-(4α-8)-catechin trimer (procyanidin C2), epicatechin-(4β-8)-epicatechin-(4β-8)-catechin trimer and epicatechin-(4β-8)-catechin-(4α-8)-epicatechin trimer derivatives) can be achieved with TMSOTf-catalyzed condensation reaction, in excellent yields. Deprotection of (+)-catechin and (−)-epicatechin trimers derivatives gives four natural procyanidin trimers in good yields.〔Efficient Stereoselective Synthesis of Proanthocyanidin Trimers with TMSOTf-Catalyzed Intermolecular Condensation. Akiko Saito, Akira Tanaka, Makoto Ubukata and Noriyuki Nakajima, Synlett, 2004, volume 6, pages 1069-1073, 〕
It has been used in Takahashi Taxol total synthesis or for chemical glycosylation reactions.

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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