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Imidazoles

Known as: Imidazoles [Chemical/Ingredient], imidazole 
Compounds containing 1,3-diazole, a five membered aromatic ring containing two nitrogen atoms separated by one of the carbons. Chemically reduced… 
National Institutes of Health

Related topics

Related topics

50 relations

Narrower (49)

1-butyl-2,3-dimethylimidazolium bromide1-butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)amide1-butyl-3-methylimidazolium tetracyanoborate1-ethyl-3-methyl imidazolium diethyl phosphate

Broader (1)

Enzyme Inhibitors

Papers overview

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Highly Cited
2010
Highly Cited
2010
Decarboxylative C-H cross-coupling of azoles.
An intermol. decarboxylative C-H cross-coupling between oxazoles and thiazoles with the rapid synthesis of functionalized… 
Review
2007
Review
2007
Heterocycle synthesis by copper facilitated addition of heteroatoms to alkenes, alkynes and arenes.
The de novo synthesis of small organic heterocyclic molecules has benefited from recent protocols for copper-facilitated… 
Highly Cited
1992
Highly Cited
1992
Cyclopiazonic acid depletes intracellular Ca2+ stores and activates an influx pathway for divalent cations in HL-60 cells.
Highly Cited
1990
Highly Cited
1990
Hydrogen bond stereochemistry in protein structure and function.
Highly Cited
1983
Highly Cited
1983
The catalytic mechanism of glutathione reductase as derived from x-ray diffraction analyses of reaction intermediates.
Highly Cited
1980
Highly Cited
1980
ADP-ribosylation of elongation factor 2 by diphtheria toxin. NMR spectra and proposed structures of ribosyl-diphthamide and its hydrolysis products.
Highly Cited
1977
Highly Cited
1977
An ultrasensitive method for the simultaneous determination of cyclic AMP and cyclic GMP in small-volume samples from blood and tissue.
Review
1967
Review
1967
Crystal structures of metal-peptide complexes.
Highly Cited
1963
Highly Cited
1963
Alkylation and identification of the histidine residues at the active site of ribonuclease.
Highly Cited
1962
Highly Cited
1962
Synthesis of purines under possible primitive earth conditions. II. Purine intermediates from hydrogen cyanide.
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