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Cited by 12 publications
(10 citation statements)
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“…Although aiming for cis -pinane, Bazhenov et al obtained 80 wt % ρ-cymene over dealuminated zeolite Y, an outstanding result in a liquid-phase operation . A slightly lower yield (70 wt %) was also obtained by Jaramillo et al with a H 3 PW 12 O 40 · x H 2 O/SiO 2 catalyst (liquid phase) .…”
Section: α-Pinene Upgrading Techniquesmentioning
confidence: 97%
“…Although aiming for cis -pinane, Bazhenov et al obtained 80 wt % ρ-cymene over dealuminated zeolite Y, an outstanding result in a liquid-phase operation . A slightly lower yield (70 wt %) was also obtained by Jaramillo et al with a H 3 PW 12 O 40 · x H 2 O/SiO 2 catalyst (liquid phase) .…”
Section: α-Pinene Upgrading Techniquesmentioning
confidence: 97%
“…Typically, a-pinene is not employed in polymerizations, as it is signicantly less reactive than b-pinene; however, it can be hydrogenated, pyrolyzed, oxidized, and isomerized into b-pinene or mixtures of other terpenes and terpenoids, such as a-phellandrene, myrcene, and menthol. [120][121][122][123] b-Pinene, a-phellandrene, myrcene, and menthol are among pinene derivatives that have been studied in controlled polymerizations. [117][118][119][120] Myrcene-and menthol-based polymers and their potential as rubbery blocks are discussed throughout Section 3.2 whereas poly(b-pinene), poly(a-phellandrene), and their BPs are reviewed in this section.…”
Section: Blocks Derived From Pine Resinmentioning
confidence: 99%
“…After solvent evaporation, was obtained 682 mg (yielding 99%) of colorless oil which was characterized as (-)-pinane by NMR/EIMS analysis and comparison with literature data. 24 (-)-Pinane.…”
Section: Hydrogenation Of (-)-A-pinenementioning
confidence: 99%