5325-97-3Relevant articles and documents
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Durland,Adkins
, (1938)
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Intramolecular Cobalt-Mediated Cycloaddition of Linear Enediynes. A Useful Synthetic Entry into Cobalt-Protected Tricyclic Dienes and Their Synthetic Elaboration
Sternberg, Ethan D.,Vollhardt, K. Peter C.
, p. 1564 - 1573 (1984)
CpCo(CO)2 undergoes reaction with the linear α,δ,ω-enediynes 4, 10, 18, 22 and 25 to give the CpCo-complexed tricyclic dienes 5, 11, 19, 20, 23, 24, 26, and possibly 27.The free ligands may be obtained in good yield by oxidative demetalation.Treatment of the dienylsilane 12 with bromine gave the desilylated aromatic 13, whereas reaction with m-chloroperbenzoic acid furnished the dienol 14 and α-trimethylsilyl β,γ-enone 15.The latter rearranged to the desilylated α,β-enone 17 with acid.Some mechanistic discussion is presented concerned with the course of the cobalt-mediated cyclization reaction.Hydride abstraction from 11 resulted in the cation 28 which underwent unexpected nucleophilic addition to both ligands, in addition to deprotonation to benzene complex 32 and the free aromatic ligand 31.
Aromatic compound hydrogenation and hydrodeoxygenation method and application thereof
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Paragraph 0094-0095; 0106-0113, (2021/05/29)
The invention belongs to the technical field of medicines, and discloses an aromatic compound hydrogenation and hydrodeoxygenation method under mild conditions and application of the method in hydrogenation and hydrodeoxygenation reactions of the aromatic compounds and related mixtures. Specifically, the method comprises the following steps: contacting the aromatic compound or a mixture containing the aromatic compound with a catalyst and hydrogen with proper pressure in a solvent under a proper temperature condition, and reacting the hydrogen, the solvent and the aromatic compound under the action of the catalyst to obtain a corresponding hydrogenation product or/and a hydrodeoxygenation product without an oxygen-containing substituent group. The invention also discloses specific implementation conditions of the method and an aromatic compound structure type applicable to the method. The hydrogenation and hydrodeoxygenation reaction method used in the invention has the advantages of mild reaction conditions, high hydrodeoxygenation efficiency, wide substrate applicability, convenient post-treatment, and good laboratory and industrial application prospects.
Catalyzed transfer hydrogenation by 2-propanol for highly selective PAHs reduction
Philippov,Chibiryaev,Martyanov
, p. 15 - 22 (2020/07/15)
Catalytic hydrogenation of mono-, di- and trinuclear aromatic compounds has been studied under hydrogen transfer conditions at 150 °C and 82 °C in 2-PrOH as a hydrogen donor and with Raney nickel as a catalyst. In contrast to conjugated or condensed aromatic rings, isolated ones demonstrated low reactivity in transfer hydrogenation (TH) that can be used to increase the hydrogenation selectivity of the reaction. So, naphthalene and biphenyl are partially hydrogenated into tetralin and cyclohexylbenzene, respectively, with excellent conversion (≥ 96 %) and selectivity (≥ 98 %) for 5–6 h at 82 °C. Increasing the reaction temperature to 150 °C results expectedly in the hydrogenation of second aromatic ring, which occurs slowly enough. Only 8 % of decaline and 42 % of dicyclohexyl, correspondingly, were obtained after 5 h at 150 °C. At the same time, TH of trinuclear anthracene and phenanthrene at 150 °C resulted in the formation of deeper hydrogenated octahydro-anthracenes and -phenanthrenes, respectively.
