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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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2015
2015
Nitroxide radicals, such as 2,2,6,6-tetramethylpiperidine 1-oxyl (TEMPO) and its derivatives, have recently been used as contrast… 
Highly Cited
2013
Highly Cited
2013
This anodic oxidation of acetophenones in the presence of methanol or ethanol not only provides a simple approach to α-ketoester… 
2013
2013
Calorimetry is used to measure the reaction enthalpies of hydrogen (H(2)) activation by 2,6-lutidine (Lut), 2,2,6,6… 
Highly Cited
2010
Highly Cited
2010
the National Natural Science Foundation of China (20772093;20972118;20832003);the Doctoral Fund of the Ministry of Education of… 
Highly Cited
2010
Highly Cited
2010
As a variety of metal-mediated biaryl formations througharomatic C H activation have been popularized, theSuzuki–Miyaura-type… 
Highly Cited
2010
Highly Cited
2010
Metalation has served well for over 80 years as a vehicle for transforming inert C[BOND]H bonds in organic compounds to reactive… 
2007
2007
Inside out approach: Twofold deprotonation of benzene by a sodium monoalkyl bisamido manganate(II) reagent derived from BuNa, 2,2… 
Highly Cited
2005
Highly Cited
2005
[reaction: see text] The reaction of dimedone with 1-(2-alkenoyl)-4-bromo-3,5-dimethylpyrazoles in THF, catalyzed by catalytic… 
1989
1989
In a previous study of structure-activity relationships of selected phenazines against Mycobacterium leprae in vitro, compounds…