1126-61-0Relevant articles and documents
Catechol-Functionalized Polyolefins
Chen, Changle,Na, Yinna
, p. 7953 - 7959 (2020)
The incorporation of comonomers during ethylene polymerization can efficiently modulate important material properties of the polyolefins. Utilizing bioresourced comonomers for the generation of high-performance polyolefin materials is attractive from a sustainability point of view. In this contribution, bioresourced eugenol and related comonomers were incorporated into polyolefins through palladium-catalyzed copolymerization and terpolymerization reactions. Importantly, high-molecular-weight catechol-functionalized polyolefins can be generated. The introduction of different metal ions induces efficient interactions with the incorporated catechol groups, leading to enhanced mechanical properties and self-healing properties. Moreover, the catechol functionality can greatly improve other properties such as surface properties, adhesion properties, and compatibilizing properties. The catechol-functionalized polyolefin was demonstrated as a versatile platform polymer for accessing various materials with dramatically different properties.
Kuwatsuka,Casida
, p. 528,529,530 (1965)
Boron Trichloride/Tetra-n-Butylammonium Iodide: A Mild, Selective Combination Reagent for the Cleavage of Primary Alkyl Aryl Ethers
Brooks, Paige R.,Wirtz, Michael C.,Vetelino, Michael G.,Rescek, Diane M.,Woodworth, Graeme F.,Morgan, Bradley P.,Coe, Jotham W.
, p. 9719 - 9721 (1999)
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Expeditious synthesis of bioactive allylphenol constituents of the genus Piper through a metal-free photoallylation procedure
Protti, Stefano,Fagnoni, Maurizio,Albini, Angelo
, p. 2868 - 2871 (2005)
Nine bioactive allylphenol (anisole) derivatives (e.g. eugenol, safrole and asaricin) present in several plants of the genus Piper have been synthesized in medium to high yield via aryl cation intermediates. This expeditious metal-free procedure involves the irradiation of the corresponding chlorophenols or chloroanisoles in a polar solvent (MeCN or, better, TFE or aqueous acetonitrile) in the presence of allyltrimethylsilane. Estragole has also been synthesized starting from the corresponding fluoroderivative and diazonium salt, though in a lower yield. The Royal Society of Chemistry 2005.
Chemical analysis and in vitro bioactivity of essential oil of laurelia sempervirens and safrole derivatives against oomycete fish pathogens
Caro, Nelson,Cuellar, Mauricio A.,Godoy, Patricio,Madrid, Alejandro,Melo, Mirna,Montenegro, Iván,Morales, Ana Lizeth,Saffirio, Valentina,Said, Bastián,Werner, Enrique
, (2021/11/08)
In this study, the essential oil (EO) from Laurelia sempervirens was analyzed by GC/MS and safrole (1) was identified as the major metabolite 1, was subjected to direct reactions on the oxygenated groups in the aromatic ring and in the side chain, and eight compounds (4 to 12) were obtained by the process. EO and compounds 4–12 were subjected to biological assays on 24 strains of the genus Saprolegnia, specifically of the species 12 S. parasitica and 12 S. australis. EO showed a significant effect against Saprolegnia strains. Compound 6 presents the highest activity against two resistant strains, with minimum inhibitory concentration (MIC) and minimum oomyceticidal concentration (MOC) values of 25 to 100 and 75 to 125 μg/mL, respectively. The results show that compound 6 exhibited superior activities compared to the commercial controls bronopol and azoxystrobin used to combat these pathogens.
Anchimerically Assisted Selective Cleavage of Acid-Labile Aryl Alkyl Ethers by Aluminum Triiodide and N, N-Dimethylformamide Dimethyl Acetal
Sang, Dayong,Yue, Huaxin,Zhao, Zhengdong,Yang, Pengtao,Tian, Juan
, p. 6429 - 6440 (2020/07/14)
Aluminum triiodide is harnessed by N,N-dimethylformamide dimethyl acetal (DMF-DMA) for the selective cleavage of ethers via neighboring group participation. Various acid-labile functional groups, including carboxylate, allyl, tert-butyldimethylsilyl (TBS), and tert-butoxycarbonyl (Boc), suffer the conditions intact. The method offers an efficient approach to cleaving catechol monoalkyl ethers and to uncovering phenols from acetal-type protecting groups such as methoxymethyl (MOM), methoxyethoxymethyl (MEM), and tetrahydropyranyl (THP) chemoselectively.