Results 171 to 180 of about 14,695 (216)
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Journal of Polymer Science, 1959
AbstractThe cyclic C6 and C8 dimers of isoprene have been prepared by thermal dimerization and their physical and chemical properties obtained. The infrared spectra of these substances are also given and are used to confirm the structures deduced chemically.
John L. Binder +2 more
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AbstractThe cyclic C6 and C8 dimers of isoprene have been prepared by thermal dimerization and their physical and chemical properties obtained. The infrared spectra of these substances are also given and are used to confirm the structures deduced chemically.
John L. Binder +2 more
openaire +1 more source
Journal of Applied Chemistry, 1969
AbstractIsoprene was dimerised by lithium naphthalene to linear isoprene dimer, a mixture of 2,6‐dimethyl‐2,6‐octadiene and 2,7‐dimethyl‐2,6‐octadiene, in 80% yield.
K. Suga +3 more
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AbstractIsoprene was dimerised by lithium naphthalene to linear isoprene dimer, a mixture of 2,6‐dimethyl‐2,6‐octadiene and 2,7‐dimethyl‐2,6‐octadiene, in 80% yield.
K. Suga +3 more
openaire +1 more source
Isomerization of OH-Isoprene Adducts and Hydroxyalkoxy Isoprene Radicals
The Journal of Physical Chemistry A, 2002This paper employs quantum chemical methods to investigate gaps in our understanding of the fates of radical intermediates in the OH-initiated degradation of isoprene. We employ two density functional theory (DFT) approaches: the well-known B3LYP functional and the recently constructed MPW1K functional.
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LOVASTATIN, ISOPRENES, AND MYOPATHY
The Lancet, 1989P A, Walravens, C, Greene, F E, Frerman
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Isoprene Emission from Plants: Why and How
Annals of Botany, 2007Thomas D Sharkey, Sharkey Thomas D
exaly
Poplar phyllosphere harbors disparate isoprene-degrading bacteria
Proceedings of the National Academy of Sciences of the United States of America, 2018Andrew T Crombie +2 more
exaly

