59919-41-4Relevant articles and documents
A regionally selective hydrogenation method for chromium-catalyzed thick cyclic aromatic hydrocarbons and olefins based on magnesium-activated ligands
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Paragraph 0020, (2022/01/10)
The present invention relates to the field of hydrogenation, specifically to a chromium-activated complex cyclic aromatic hydrocarbons and olefins promoted by magnesium-activated ligands regionally selective hydrogenation method, which is based on the in situ reduction strategy of magnesium, with biimides as ligands, CrCl2 as catalyst precursors, to construct an efficient low-costchromium hydrogenation system, under mild conditions, to achieve unilateral cyclic hydrogenation of thick ring aromatic hydrocarbons and high-selective hydrogenation of olefins. The system of the present invention is suitable for a variety of substrates of fused cyclic aromatic hydrocarbons, such as tetraphenyl, benzoanthracene, pentabenzo and alfalfa and the like. This provides a simple and efficient strategy and pathway for the synthesis of partially saturated thick cyclic aromatic hydrocarbon compounds.
Synthese et proprietes du diethyl-2,6 naphtalene et de quelques derives nitres. Resonance magnetique nucleaire du proton et du carbone-13
Richer, Jean-Claude,Catelani, Giorgio,Mechin, Bernard
, p. 458 - 463 (2007/10/02)
We report the synthesis of 2,6-diethyl naphthalene from 2,6 dimethyl naphthalene and of some mono and dinitrated derivatives.Examination of the 1H and 13C NMR spectra shows that the sterical constrained ethyl group affects carbons C1 and C3 of the naphthalene ring and causes a shift in the same direction and of intermediary magnitude to those caused by the methyl and t-butyl groups.These results confirms the influence on C1 and C3 of the specific anisotropic term of the OCH3 substituent.
