Results 11 to 20 of about 1,079 (262)

High Accuracy Measurements of OH Reaction Rate Constants and IR Absorption Spectra: Substituted 2-Propanols

open access: yes, 2016
Rate constants for the gas phase reactions of OH radicals with 2-propanol and three fluorine substituted 2-propanols, (CH3)2CHOH (k0), (CF3)2CHOH (k1), (CF3)2C­(OH)­CH3 (k2), and (CF3)3COH (k3), were measured using a flash photolysis resonance ...
Vladimir L. Orkin (1777357)   +2 more
core   +7 more sources

Toward the sustainable synthesis of propanols from renewable glycerol over MoO3-Al2O3 supported palladium catalysts [PDF]

open access: yes, 2018
The catalytic conversion of glycerol to value-added propanols is a promising synthetic route that holds the potential to overcome the glycerol oversupply from the biodiesel industry.
Sankar Bhattacharya   +3 more
core   +1 more source

Synthesis of N-Substituted Diamino-Propanols and their Physiological Effects [PDF]

open access: yes, 1964
The p-toluiclinc-epichlorohydrin 1:1 addition compound has been reacted with pipericline, pyrrolicline, and morpholine to give disubstitutecl 2-propanols. 1-(p-Toluiclino)-3-pyrrolidino-2-propanol was fed to male rats and organ and body weights measured.
Pennington, F. C., Mortenson, Kathren
core   +1 more source

Homochiral (R)- and (S)-1-heteroaryl- and 1-aryl-2-propanols via microbial redox

open access: yes, 1998
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%).
MEDICI, Alessandro   +11 more
core   +1 more source

Discovery of Chiral N,N-Disubstituted Trifluoro-3-amino-2-propanols as Potent Inhibitors of Cholesteryl Ester Transfer Protein

open access: yes, 2016
Discovery of Chiral N,N-Disubstituted Trifluoro-3-amino-2-propanols as Potent Inhibitors of Cholesteryl Ester Transfer ...
Deborah M. Heuvelman (3011085)   +15 more
core   +1 more source

HEALTH RISKS FROM TOXIC CONTAMINANTS FORMED DURING THE PROCESSING OF VEGETABLE OILS AND FATS

open access: yesJournal of Engineering Science (Chişinău)
The purpose of this review was to summarize current research findings and unify ideas regarding methods to reduce the health risks to consumers posed by toxic contaminants, such as chloropropanols, glycidols, and their esters ...
GUREV, Angela   +2 more
doaj   +1 more source

Bupropion hydrobromide propanol hemisolvate [PDF]

open access: yesActa Crystallographica Section E Structure Reports Online, 2011
The title compound {systematic name: N-[1-(3-chloro-phen-yl)-1-oxopropan-2-yl]-tert-butanaminium bromide propanol hemisolvate}, C(13)H(19)ClNO(+)·Br(-)·0.5C(3)H(8)O, crystallizes with two independent bupropion hydro-bromide ion pairs and a solvent 1-propanol mol-ecule in the asymmetric unit.
Gu-Ping Tang   +3 more
openaire   +3 more sources

Digital Light Processing of Thermoplastic Poly(methyl methacrylate) Photoresin Combined With Solvent Vapor Smoothing

open access: yesAdvanced Engineering Materials, EarlyView.
A thermoplastic PMMA‐based photoresin enables high‐resolution DLP printing followed by solvent‐vapor smoothing. The treatment reduces staircase‐induced surface roughness from 2.33 µm to 129 nm and increases visible‐light transmittance from approximately 30% to 80%, providing a route toward transparent PMMA components for rapid prototyping and non ...
Rozhin Heydarpour   +5 more
wiley   +1 more source

The Trend in Mitigation Strategies of 3-Monochloropropane-1,2-diol and Glycidyl Esters in Edible Vegetable Oils: Today and Tomorrow

open access: yesFood Technology and Biotechnology
3-Monochloropropane-1,2-diol (3-MCPD) and its esters, which have carcinogenic and genotoxic effects, are contaminants induced by high-temperature that have been detected in refined oils and fatty foods.
Kıvılcım Yıldız   +2 more
doaj   +1 more source

Selective Catalytic sp3 C–O Bond Cleavage with C–N Bond Formation in 3-Alkoxy-1-propanols

open access: yes, 2016
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.
Cheng Chen (136164)   +1 more
core   +1 more source

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