Results 201 to 210 of about 42,045 (302)
Selective catalytic sp3 C-O bond cleavage with C-N bond formation in 3-alkoxy-1-propanols.
The ruthenium catalyzed selective sp3 C–O cleavage with amide formation was reported in reactions of 3-alkoxy-1-propanol derivatives and amines. The cleavage only occurs at the C3–O position even with 3-benzyloxy-1-propanol.
C. Chen, S. Hong
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Excess enthalpies of binary mixtures of butylamines + propanols at 298.15 K
Journal of Thermal Analysis and Calorimetry, 2013Takayoshi Kimura +2 more
exaly +2 more sources
Homochiral (R)- and (S)-1-heteroaryl- and 1-aryl-2-propanols via microbial redox
Preparation of various optically active heteroaryl propanols for microbial redox is described. The kinetic resolution of the racemic propanols is obtained via oxidation with Bacillus stearothermophilus ( R-alcohols, ee 74-100%).
M. Fogagnolo +5 more
semanticscholar +2 more sources
Journal of Molecular Catalysis B: Enzymatic, 2005
Toshifumi Miyazawa, Takashi Murashima
exaly +2 more sources
Toshifumi Miyazawa, Takashi Murashima
exaly +2 more sources
Poisoning with 1-propanol and 2-propanol
Human & Experimental Toxicology, 20071-Propanol and 2-propanol are isomers of an alcohol with three carbons. They are colorless liquids with a sweet odor. 1-Propanol is metabolized by alcohol dehydrogenase to propionic acid and presents with metabolic acidosis and elevated anion gap, whereas 2-propanol is metabolized by alcohol dehydrogenase to acetone and presents with rapidly developing
M, Vujasinovic +4 more
openaire +2 more sources
Microbial production of propanol
Biotechnology Advances, 2016Both, n-propanol and isopropanol are industrially attractive value-added molecules that can be produced by microbes from renewable resources. The development of cost-effective fermentation processes may allow using these alcohols as a biofuel component, or as a precursor for the chemical synthesis of propylene.
Walther, Thomas, François, Jean Marie
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