Results 201 to 210 of about 54,393 (252)
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Peculiarities of β‐Pinene Autoxidation

ChemSusChem, 2011
AbstractThe thermal oxidation of the renewable olefin β‐pinene with molecular oxygen was experimentally and computationally investigated. Peroxyl radicals abstract weakly bonded allylic hydrogen atoms from the substrate, yielding allylic hydroperoxides (i.e., myrtenyl and pinocarvyl hydroperoxide).
Ulrich, Neuenschwander   +2 more
openaire   +2 more sources

Gamma-radiolysis of chiral terpenes: α-(−)pinene and α-(+)pinene

Journal of Radioanalytical and Nuclear Chemistry, 2007
The terpenes α-(+)-pinene, and α-(−)pinene have been radiolyzed at radiation doses of 150, 300 and 600 kGy. The radiolyzed samples have been analyzed by FT-IR spectroscopy and polarimetry. Both α-(+)-, α-(−)-pinenes show a linear trend to radioracemization as a function of the radiation dose administered ≈2.5·10−3 [α]D/kGy.
openaire   +1 more source

Ueber Pinen

Berichte der deutschen chemischen Gesellschaft, 1895
Ferd. Tiemann, F. W. Semmler
openaire   +1 more source

Molecular mechanism for rapid autoxidation in α-pinene ozonolysis

Nature Communications, 2021
Siddharth Iyer   +2 more
exaly  

Ozonolysis of alpha-pinene and beta-pinene: kinetics and mechanism.

The Journal of chemical physics, 2006
A combined quantum-chemical and RRKM/ME (ME--master equation) approach is employed to investigate the structures, energetics, and kinetics of intermediate and stable species, and the yields of stabilized carbonyl oxides and OH radicals from the alpha-pinene and beta-pinene ozonolysis reactions.
Dan, Zhang, Renyi, Zhang
openaire   +1 more source

α-Pinene: A never-ending story

Phytochemistry, 2021
Christian Steuer
exaly  

α-Pinene

Food and Cosmetics Toxicology, 1978
openaire   +2 more sources

β-Pinene

Food and Cosmetics Toxicology, 1978
openaire   +2 more sources

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