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2,2,6,6-tetramethylpiperidide

Known as: 2,2,6,6-tetramethylpiperidine 
National Institutes of Health

Papers overview

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Review
2018
Review
2018
N-Oxyl compounds represent a diverse group of reagents that find widespread use as catalysts for the selective oxidation of… Expand
Highly Cited
2015
Highly Cited
2015
A metal-free catalyst born of frustration Boron (a Lewis acid) and nitrogen or phosphorus fragments (both Lewis bases) tend to… Expand
Highly Cited
2014
Highly Cited
2014
For many biological and biomedical studies, it is essential to detect the production of (1)O2 and quantify its production yield… Expand
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Highly Cited
2011
Highly Cited
2011
Heteroarenes equipped with aryl groups (heterobiaryls) are often found in biologically active compounds, organic materials, and… Expand
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Highly Cited
2010
Highly Cited
2010
The frustrated Lewis pair system consisting of 2 equiv of 2,2,6,6-tetramethylpiperidine (TMP) and tris(pentafluorophenyl)borane… Expand
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Highly Cited
2009
Highly Cited
2009
In the presence of 2,2,6,6-tetramethylpiperidine (TMP) 1,8-bis(dipentafluorophenylboryl)naphthalene has been found to activate H2… Expand
Highly Cited
2008
Highly Cited
2008
In industrially important reactions, such as hydroformylation and hydrogenation, H2 gas serves as a reducing agent and/or a… Expand
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Highly Cited
2008
Highly Cited
2008
Pyruvate ferredoxin oxidoreductase (PFOR), which catalyzes the oxidative decarboxylation of pyruvate to form acetyl-CoA and CO2… Expand
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Highly Cited
2004
Highly Cited
2004
Exposure of isolated spinach thylakoids to high intensity illumination (photoinhibition) results in the well-characterized… Expand
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Highly Cited
2001
Highly Cited
2001
Summary. Molecular oxygen in electronic singlet state is a very powerful oxidant. Its damaging action in a variety of biological… Expand
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