2,6-lutidine

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

Papers overview

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2011
2011
Aerobic oxidative cross-coupling reactions between alkynes and boronic acids under mild conditions catalyzed by low loadings of a… (More)
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2011
2011
Organoboranes have attracted great attention owing to their interesting photophysical properties, which enable promising… (More)
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2009
2009
Classical Lewis acid-base adducts, previously thought to be unreactive, can provide access to the unique reactivity of frustrated… (More)
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2008
2008
When fluctuating fields are confined between two surfaces, long-range forces arise. A famous example is the quantum… (More)
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2008
2008
We studied the micelle formation of a diblock copolymer of styrene and ethylene oxide in mixtures of 2,6-dimethylpyridine (2,6… (More)
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2006
2006
IR spectroscopy of probe molecules (pyridine, 2,6-dimethylpyridine, and CO) as well as high-resolution solid state NMR and… (More)
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2004
2004
Acetal functions are recognized as good protecting groups of carbonyl groups. Although many deprotecting methods of acetals to… (More)
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2004
2004
A series of 8-heteroarylthiomethyldipyridodiazepinone derivatives were prepared and evaluated for their antiviral profile against… (More)
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1998
1998
cis-[Amminedichloro(2-methylpyridine)] platinum(II) (AMD473) is a novel sterically hindered anti-tumour compound designed to… (More)
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1984
1984
Multinuclear (31P, 13C, 2H, and 1H) Fourier-transform NMR spectroscopy, with and without isotopically enriched materials, was… (More)
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