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trimethyloxonium

Known as: Oxonium, trimethyl- 
National Institutes of Health

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1 relation

Broader (1)

Onium Compounds

Papers overview

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Highly Cited
2014
Highly Cited
2014
Rhodium(II)-catalyzed stereocontrolled synthesis of dihydrofuran-3-imines from 1-tosyl-1,2,3-triazoles.
Rhodium(II) acetate catalyzes the denitrogenative transformation of 5-substituted and 4,5-disubstituted 1-sulfonyl-1,2,3… 
Highly Cited
2013
Highly Cited
2013
From ynamides to highly substituted benzo[b]furans: gold(I)-catalyzed 5-endo-dig-cyclization/rearrangement of alkylic oxonium intermediates.
A series of arylynamides with alkyloxy groups at the ortho position of the aryl group was prepared through a short alkylation… 
2011
2011
Expedient route to the tigliane-daphnane skeleton via oxonium ylide [1,2]-shift.
A short, stereoselective approach to the fused tricyclic carbon skeleton found in the tigliane and daphnane classes of diterpene… 
2003
2003
Cyclooctanoid ring systems from mixed acetals via heteroatom-assisted [1,2]-shift of oxonium ylides.
Cyclic mixed acetals with pendant diazoketone side chains undergo efficient rearrangement to ether-bridged cyclooctanoid systems… 
Highly Cited
2001
Highly Cited
2001
Iterative approach to polycyclic ethers based on stereoselective oxonium ylide [2,3]-shifts.
General. Reactions were carried out in flame-dried glassware under a positive nitrogen atmosphere unless otherwise stated… 
Highly Cited
1989
Highly Cited
1989
Role of surface electrostatics in the operation of a high-conductance Ca2+-activated K+ channel.
This paper demonstrates that local electric fields originating from negatively charged groups on a K+-specific ion channel modify… 
Highly Cited
1986
Highly Cited
1986
Generation and rearrangements of oxonium ylides.
Highly Cited
1986
Highly Cited
1986
Intramolecular generation and [2,3]-sigmatropic rearrangement of oxonium ylides.
1975
1975
Preferential chemical modification of a binding subsite on the acetylcholine receptor.
1972
1972
The number of catalytically essential carboxyl groups in pepsin. Modification of the enzyme by trimethyloxonium fluoroborate.
Pepsin has been modified by reaction with [14C]trimethyloxonium fluoroborate at pH 5.0. The loss of catalytic activity consequent… 
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