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pinacolone

Known as: 3,3-dimethyl-2-butanone 
 
National Institutes of Health

Papers overview

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2012
2012
Abstract Rhenium (I, III–V or VII) complexes bearing N -donor or oxo-ligands catalyse the Baeyer–Villiger oxidation of cyclic and… Expand
2011
2011
In this report, we present a regioselective oxidation of a series bacteriochlorins, which on reacting with either ferric chloride… Expand
2010
2010
ABSTRACT We isolated three Sphingobium fuliginis strains from Phragmites australis rhizosphere sediment that were capable of… Expand
Highly Cited
2010
Highly Cited
2010
To provide improved understanding of guest-host interactions in clathrate hydrates, we present some correlations between guest… Expand
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Highly Cited
2010
Highly Cited
2010
The development of transition-metal-catalyzed methods for the direct functionalization of C H bonds has attracted much attention… Expand
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Highly Cited
2005
Highly Cited
2005
When the reaction of aromatic ketones with arylboronates (arylboronic acid esters) using RuH(2)(CO)(PPh(3))(3) (3) as a catalyst… Expand
2003
2003
Nature of organic ion radicals and their ground-state electron structure formation of organic ion radicals basic principles of… Expand
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Highly Cited
2001
Highly Cited
2001
To investigate the effects of electron-donating and electron-withdrawing substituents upon the reaction of porphyrins with osmium… Expand
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1999
1999
Abstract Treatment of a variety of ketones with lithium diisopropylamide followed by p -toluenesulfonyl chloride gives… Expand
Highly Cited
1986
Highly Cited
1986
Reaction of 3,3-dimethyl-2-butanone (pinacolone) with alkali amide bases yields crystalline enolates. These compounds were… Expand
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