Results 221 to 230 of about 10,973 (280)

Attractive Noncovalent Interactions versus Steric Confinement in Asymmetric Supramolecular Catalysis. [PDF]

J Am Chem Soc
Craescu CV, David CD, Heafner ED, Raymond KN, Bergman RG, Toste FD.   +5 more
europepmc   +1 more source

Electron paramagnetic resonance detection of superoxide in a murine model of acute lung injury. [PDF]

Discov Imaging
Elajaili HB, Dee N, Hovey T, Canny A, Amassah G, Posey J, Rinard GA, Kao JPY, Eaton SS, Eaton GR, Nozik ES.   +10 more
europepmc   +1 more source

Spatiotemporally controlled drug release via a click-release system utilizing mono-alkyl-hydroxylamine and cyclooctyne chemistry. [PDF]

Nat Commun
Xu X, Tong X, Shi Y, Wang X, Chen Y, Wang Y, Cheng M, Chen S, Hao H, Liang Y, Guo W, Zheng Y.   +11 more
europepmc   +1 more source

Nickel-catalyzed highly diastereo- and enantioselective hydroaminocarbonylation and hydrocarboxylation of cyclopropenes. [PDF]

Nat Commun
Wu J, Yu B, Gao B, Huang H.
europepmc   +1 more source

Studies on Asymmetric Synthesis of Chiral N-Hydroxylamines and Secondary Amines [PDF]

ソン, グン, 孫, 軍
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Potassium Hydroxylamine Complexes

Inorganic Chemistry, 2008
Potassium complexes of N,N-dialkylhydroxylamines [KONR2, R=Me (1a), iPr (2a), CH2C6H5] were synthesized by the deprotonation of the corresponding N, N-dialkylhydroxylamines with KH. 1a and 1b [(KONMe2)(HONMe2)] dissolve in THF under the addition of an additional equiv of the parent hydroxylamine to give 1b and [(KONiPr2)(HONiPr2)(THF)] 2b. 1b, 2b and [(
Venugopal, Ajay, Berger, Raphael, Willner, Alexander, Pape, Tania, Mitzel, Norbert W.   +4 more
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Techniques for Investigating Hydroxylamine Disproportionation by Hydroxylamine Oxidoreductases

2011
Hydroxylamine, an important intermediate in ammonia oxidation by ammonia oxidizing bacteria (AOB), is inherently unstable with respect to disproportionation. The process is slow in neutral solutions, but could potentially be catalyzed by enzymes such as the hydroxylamine oxidoreductases, which normally catalyze the oxidation of ammonia to nitrite in ...
A Andrew, Pacheco, Jennifer, McGarry, Joshua, Kostera, Angel, Corona   +3 more
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Hydroxylamine metabolism in Pseudomonas PB16: involvement of a novel hydroxylamine oxidoreductase

Antonie van Leeuwenhoek, 1997
Pseudomonas strain PB16, a Gram-negative heterotrophic nitrifying bacterium closely related to Pseudomonas azalaica on the basis of 16 S rDNA analysis, was able to use hydroxylamine as an additional energy source during growth in acetate limited chemostat cultures giving an increased biomass yield.
Jetten, M.S.M. (author), De Bruijn, P. (author), Kuenen, J.G. (author)   +2 more
openaire   +3 more sources

The reaction of adenosine with hydroxylamine

Biochimica et Biophysica Acta (BBA) - Nucleic Acids and Protein Synthesis, 1971
Abstract Adenosine reacts with hydroxylamine to give N (6)-hydroxyadenosine at 1 200 th the rate of the corresponding reaction with cytidine. N (6)-Hydroxyadenosine is in turn converted to adenosine-1-oxide and the latter may also be a primary product of the reaction. 1-Methyladenine and hydroxylamine afford adenine-1-oxide.
D M, Brown, M R, Osborne
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The hydroxylamine reductase of mitochondria

Archives of Biochemistry and Biophysics, 1969
Abstract The hydroxylamine reductase of rat liver mitochondria has been studied. This enzyme reduces hydroxylamine (HA) to ammonia, using NADH; the stoichiometry of the reaction is 1:1:1. Although extensive efforts have been made to solubilize the enzyme, it remains firmly attached to the mitochondrial membrane.
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