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Journal articles on the topic 'Aryl Ethers'

Author: Grafiati

Published: 4 June 2021

Last updated: 3 February 2022

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1

Holsboer, D. H., J. W. Scheeren, and A. P. M. van Der Veek. "Aryl dichloromethyl ethers." Recueil des Travaux Chimiques des Pays-Bas 90, no. 5 (September 2, 2010): 556–61. http://dx.doi.org/10.1002/recl.19710900512.

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2

Fernandes, Rodney A., Sachin P. Gholap, and Sandip V. Mulay. "A facile chemoselective deprotection of aryl silyl ethers using sodium hydride/DMF and in situ protection of phenol with various groups." RSC Adv. 4, no. 32 (2014): 16438–43. http://dx.doi.org/10.1039/c4ra00842a.

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3

Sang, Dayong, Jiahui Wang, Yun Zheng, Jianyuan He, Caili Yuan, Qing An, and Juan Tian. "Carbodiimides as Acid Scavengers in Aluminum Triiodide Induced Cleavage of Alkyl Aryl Ethers." Synthesis 49, no. 12 (March 14, 2017): 2721–26. http://dx.doi.org/10.1055/s-0036-1588755.

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A practical procedure for the cleavage of alkyl aryl ethers containing labile functional groups has been developed using aluminum triiodide as the ether cleaving reagent. Carbodiimides, typically used as dehydration reagents for the coupling of amines and carboxylic acids to yield amide bonds, are found to be effective hydrogen iodide scavengers that prevent acid-labile groups from deterioration. The method is applicable to variant alkyl aryl ethers such as eugenol, vanillin, ortho-vanillin and methyl eugenol. Suitable substrates are not limited to alkyl o-hydroxyphenyl ethers.

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4

Thanh, Nguyen D., Do S. Hai, Vu T. N. Bich, Pham T. T. Hien, Nguyen T. K. Duyen, Nguyen T. Mai, Tran T. Dung, et al. "Using Sodium Hydride and Potassium Carbonate as Bases in Synthesis of Substituted 2-Amino-4-aryl-7-propargyloxy-4H-chromene-3-carbonitriles." Current Organic Synthesis 16, no. 3 (June 17, 2019): 423–30. http://dx.doi.org/10.2174/1570179416666190104124652.

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Aims and Objective: 1-Alkynes are the important precursors for the CuAAC click chemistry. The hybrid of 1,2,3-triazole ring to the chromene ring and sugar moiety could bring some remarkable biological properties. Propargyl derivatives are usually used in the click chemistry. This article reported the synthesis of 2-amino-4-aryl-7-propargyloxy-4-aryl-4H-chromene-3-carbonitriles using propargyl bromide as alkylation agent and the use of potassium carbonate and sodium hydride as bases in the conversion of 2-amino-4-aryl-7- hydroxy-4-aryl-4H-chromene-3-carbonitriles into corresponding propargyl ethers in Williamson’s ether synthesis. Materials and Methods: The use of CTAB for the synthesis of benzylidene malononitriles and anhydrous potassium carbonate as a catalyst in absolute ethanol in the synthesis of 2-amino-7-hydroxy-4H-chromene-3- carbonitriles is an efficient and simple synthetic method. Propargyl ether compounds of these 4H-chromene-3- carbonitriles were obtained from the alkylation reaction by propargyl bromide. Two procedures were applied: K2CO3 as a base in acetone solvent (Procedure A) and NaH as a base in DMF solvent (Procedure B). The single-crystal X-ray structure of propargyl ether 5e has been studied. Results: The use of K2CO3 and NaH as bases in the Williamson’s ether synthesis from 2-amino-7-hydroxy-4Hchromene- 3-carbonitriles showed that Procedure B was the better route and gave ethers in the higher yields. 2- Amino-4-aryl-7-propargyloxy-4-aryl-4H-chromene-3-carbonitriles were obtained from corresponding 7- hydroxy-4H-chromene-3-carbonitriles. Yields of ethers 5a-i were 70−89% and 80−96%, respectively depending on the used procedures. Conclusion: The described methods are simple, clean and environmentally friendly alternatives for the preparation of 2-amino-4-aryl-7-hydroxy-4H-chromene-3-carbonitriles. The conditions for the transformation of these compounds into propargyl ethers include dried DMF as a solvent, NaH as a base and reaction time of 2 h at the room temperature. A series of 2-amino-4-aryl-7-hydroxy-4-aryl-4H-chromene-3-carbonitriles were obtained based on investigated reaction condition.

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5

Saunders, D. G. "Direct Conversion of Aryl Silyl Ethers to Alkyl Aryl and Diaryl Ethers." Synthesis 1988, no. 05 (1988): 377–79. http://dx.doi.org/10.1055/s-1988-27579.

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6

Arisawa, Mieko, Masahiko Yamaguchi, Saori Tanii, Takaya Tougo, and Kiyofumi Horiuchi. "Thieme Chemistry Journals Awardees – Where Are They Now? Rhodium-Catalyzed Synthesis of Unsymmetric Di(heteroaryl) Ethers Using Heteroaryl Exchange Reaction." Synlett 28, no. 13 (April 27, 2017): 1601–7. http://dx.doi.org/10.1055/s-0036-1588801.

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Unsymmetric di(heteroaryl) ethers were synthesized by the rhodium-catalyzed heteroaryl exchange reaction of heteroaryl aryl ethers and heteroaryl esters at equilibrium. Diverse unsymmetric di(heteroaryl) ethers containing five- and six-membered heteroarenes were obtained. Di(heteroaryl) ethers can be synthesized starting from diaryl ethers, because heteroaryl aryl ethers are obtained by the heteroaryl exchange reaction of diaryl ethers.

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7

Han, Jianhua, Kuanyu Yuan, Cheng Liu, Jinyan Wang, and Xigao Jian. "Donor–acceptor copolymers containing the phthalazinone–thiophene structure synthesized by classical nucleophilic aromatic polymerization." RSC Advances 5, no. 39 (2015): 30445–55. http://dx.doi.org/10.1039/c5ra03771a.

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8

Frey, Guido D., and Stephan D. Hoffmann. "Synthesis of ferrocenyl aryl ethers via Cu(I)/phosphine catalyst systems." Zeitschrift für Naturforschung B 70, no. 1 (January 1, 2015): 65–70. http://dx.doi.org/10.1515/znb-2014-0178.

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AbstractFerrocenyl aryl ethers can be synthesized in good yields by Cu(I)/phosphine-catalyzed coupling reactions from iodoferrocene or 1,1′-dibromoferrocene and various phenols in toluene, using Cs2CO3 or K3PO4 as a base. For the first time a solid-state structure of a ferrocenyl-1,1′-diaryl ether [1,1′-di(4-tert-butylphenoxy)ferrocene] has been determined from single-crystal X-ray data. The mixed ferrocenyl aryl ether 1-(4-tert-butylphenoxy)-1′-(2,4-dimethylphenoxy)ferrocene was prepared in a two-step synthetic protocol.

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9

Törincsi, Mercedesz, Melinda Nagy, Tamás Bihari, András Stirling, Pál Kolonits, and Lajos Novak. "Rearrangements of Cycloalkenyl Aryl Ethers." Molecules 21, no. 4 (April 19, 2016): 503. http://dx.doi.org/10.3390/molecules21040503.

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10

Törincsi, Mercedesz, Pál Kolonits, Jenő Fekete, and Lajos Novak. "Rearrangement of Aryl Geranyl Ethers." Synthetic Communications 42, no. 21 (November 2012): 3187–99. http://dx.doi.org/10.1080/00397911.2011.579799.

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11

Rashmi, P., Gopal Krishna Rao, Kshama Devi, B. G. Shivananda, G. R. Swetha, and G. A. Suneetha. "Novel Aryl Ether Derivatives as Antiinflammatory and Analgesics." E-Journal of Chemistry 8, no. 3 (2011): 1401–7. http://dx.doi.org/10.1155/2011/545403.

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The diaryl ether moieties have attracted considerable attention of medicinal chemists as they are endowed with a wide range of diverse biological activities. The present study involves synthesis, characterization of some new aryl ethers and evaluation of their antiinflammatory and analgesic activity. A series of new aryl ether derivatives[4(a-h), 5]were prepared by Ullmann’s ether condensation. The structures of new compounds are supported by their IR,1H NMR and Mass spectra. The new derivatives were evaluated for their antiinflammatory and analgesic activity. Among the tested, compound3has shown better antiinflammatory and analgesic activity.

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12

Ren, Yun-Lai, Jianji Wang, Xinzhe Tian, Fangping Ren, Xinqiang Cheng, and Shuang Zhao. "Direct Conversion of Benzyl Ethers into Aryl Nitriles." Synlett 29, no. 18 (October 16, 2018): 2444–48. http://dx.doi.org/10.1055/s-0037-1611062.

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A direct method was developed for the conversion of benzyl ethers into aryl nitriles by using NH4OAc as the nitrogen source and oxygen as the terminal oxidant with catalysis by TEMPO/HNO3; the method is valuable for both the synthesis of aromatic nitriles and for the deprotection of ether-protected hydroxy groups to form nitrile groups in multistep organic syntheses.

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13

Ankala, Sudha V., and Gabriel Fenteany. "Selective deprotection of either alkyl or aryl silyl ethers from aryl, alkyl bis-silyl ethers." Tetrahedron Letters 43, no. 27 (July 2002): 4729–32. http://dx.doi.org/10.1016/s0040-4039(02)00942-5.

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14

Yin, Biao, Manlin Fu, Lei Wang, Jiang Liu, and Qing Zhu. "Dual ligand-promoted palladium-catalyzed nondirected C–H alkenylation of aryl ethers." Chemical Communications 56, no. 22 (2020): 3293–96. http://dx.doi.org/10.1039/d0cc00940g.

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This catalytic system promoted by dual ligand catalyst readily achieved the highly efficient alkenylation of alkyl aryl ethers, cyclic aryl ethers, and diphenyl oxides. Moreover, the methodology was employed for the late-stage modification of drug.

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15

Ramadhar, Timothy, Jun-ichi Kawakami, and Robert Batey. "Sequential O-Arylation/Lanthanide(III)-Catalyzed [3,3]-Sigmatropic Rearrangement of Bromo-Substituted Allylic Alcohols." Synlett 28, no. 20 (August 25, 2017): 2865–70. http://dx.doi.org/10.1055/s-0036-1590890.

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Lanthanide(III)-catalyzed aryl-Claisen rearrangement of substrates bearing halo-substituted allyl groups, specifically 2-bromoallyl aryl ethers, afford ortho-2-bromoallylphenols. Aryl ether substrates were synthesized from brominated allylic alcohols via Mitsunobu reaction, Cu(II)-catalyzed arylation using potassium aryltrifluoroborate salts, or SNAr reaction. Aryl-Claisen rearrangements proceeded in moderate to excellent yields using Eu(III) catalysis. The alkenylbromide functionality remains intact, illustrating the compatibility of synthetically important alkenylhalides during C–O/C–C σ-bond migration processes. Subsequent derivatization of the ortho-2-bromoallylphenol products through O-alkylation or C-arylation/alkenylation via Suzuki–Miyaura cross-coupling demonstrate the potential to access densely-functionalized molecules.

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16

Patel, Purvish, and Sophie A. L. Rousseaux. "Nickel-Catalyzed Amination of α-Aryl Methyl Ethers." Synlett 31, no. 05 (October 28, 2019): 492–96. http://dx.doi.org/10.1055/s-0039-1690718.

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α-Aryl amines are prevalent in pharmaceutically active compounds and natural products. Herein, we describe a Ni-catalyzed protocol for their synthesis from readily available α-aryl ethers. While α-aryl ethers have been used as electrophiles in Ni-catalyzed C–C bond formations, their use in C–heteroatom bond formation is much less prevalent. Preliminary mechanistic insight suggests that oxidative addition is facilitated by an anionic ligand and that reductive elimination is a reversible process.

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17

Oriyama, Takeshi, Kojiro Noda, and Kaori Yatabe. "Highly Efficient and Convenient Methods for the Direct Conversion of Aryl Silyl Ethers and Aryl Acetates into Aryl Alkyl Ethers." Synlett 1997, no. 6 (June 1997): 701–3. http://dx.doi.org/10.1055/s-1997-3267.

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18

Wang, Zhi-Min, Xiu-Lian Zhang, and K. Barry Sharpless. "Asymmetric dihydroxylation of aryl allyl ethers." Tetrahedron Letters 34, no. 14 (April 1993): 2267–70. http://dx.doi.org/10.1016/s0040-4039(00)77590-3.

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19

Audier, Henri, Dorothée Berthomieu, Danielle Leblanc, and Thomas Hellman Morton. "Multiple protonation sites in aryl ethers." International Journal of Mass Spectrometry and Ion Processes 175, no. 1-2 (May 1998): 133–47. http://dx.doi.org/10.1016/s0168-1176(98)00122-0.

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20

Fukui, Hiroyuki, Hiroshi Murata, Ken-ichi Sanechika, and Masanori Ikeda. "Lubricity of fluorinated alkyl aryl ethers." Journal of Fluorine Chemistry 103, no. 2 (April 2000): 129–34. http://dx.doi.org/10.1016/s0022-1139(99)00293-6.

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21

Chang, Meng-Yang, Hang-Yi Tai, Chung-Yu Tsai, Yi-Jing Chuang, and Ying-Ting Lin. "Synthesis of substituted aryl enol ethers." Tetrahedron Letters 55, no. 47 (November 2014): 6482–85. http://dx.doi.org/10.1016/j.tetlet.2014.10.018.

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22

Chodakowski, Jan, Tomasz Kliś, and Janusz Serwatowski. "Regioselective lithiation of aryl benzyl ethers." Tetrahedron Letters 46, no. 12 (March 2005): 1963–65. http://dx.doi.org/10.1016/j.tetlet.2005.02.006.

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23

Liu, Baijun, Wei Hu, Shuang Zhao, Chunhai Chen, Zhongwen Wu, and Toshihiko Matsumoto. "Methylated and Trifluoromethylated Poly(aryl ethers)." Polymer Journal 35, no. 8 (August 2003): 628–33. http://dx.doi.org/10.1295/polymj.35.628.

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24

Zhang, Ming-Xin, Xu-Hong Hu, Yun-He Xu, and Teck-Peng Loh. "Selective Dealkylation of Alkyl Aryl Ethers." Asian Journal of Organic Chemistry 4, no. 10 (August 21, 2015): 1047–49. http://dx.doi.org/10.1002/ajoc.201500196.

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25

de Kruijff, Goswinus H. M., and Siegfried R. Waldvogel. "Electrochemical Synthesis of Aryl Methoxymethyl Ethers." ChemElectroChem 6, no. 16 (February 12, 2019): 4180–83. http://dx.doi.org/10.1002/celc.201801880.

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26

Mastral, Ana M., Vicente L. Cebolla, and JoséM Gavilán. "Alkyl aryl ethers in lignite solubilization." Fuel 64, no. 3 (March 1985): 316–20. http://dx.doi.org/10.1016/0016-2361(85)90417-x.

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27

Higashida, Kosuke, Masaya Sawamura, and Vishal Kumar Rawat. "Nickel-Catalyzed Homocoupling of Aryl Ethers with Magnesium Anthracene Reductant." Synthesis 53, no. 18 (May 17, 2021): 3397–403. http://dx.doi.org/10.1055/a-1509-5954.

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AbstractNickel-catalyzed reductive homocoupling of aryl ethers has been achieved with Mg(anthracene)(thf)3 as a readily available low-cost reductant. DFT calculations provided a rationale for the specific efficiency of the diorganomagnesium-type two-electron reducing agent. The calculations show that the dianionic anthracene-9,10-diyl ligand reduces the two aryl ether substrates, resulting in the homocoupling reaction through supply of electrons to the Ni-Mg bimetallic system to form organomagnesium nickel(0)-ate complexes, which cause two sequential C–O bond cleavage reactions. The calculations also showed cooperative actions of Lewis acidic magnesium atoms and electron-rich nickel atoms in the C–O cleavage reactions.

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28

Dhanalekshmi, S., K. K. Balasubramaniandy, and C. S. Venkatachalamdy. "Electrochemical behaviour of 3,3-sigmatropic systems - anodic oxidation of aryl allyl ethers and aryl propargyl ethers." Tetrahedron Letters 32, no. 51 (December 1991): 7591–92. http://dx.doi.org/10.1016/0040-4039(91)80542-e.

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29

Keipour, Hoda, Abolfazl Hosseini, Amir Afsari, Razieh Oladee, Mohammad A. Khalilzadeh, and Thierry Ollevier. "CsF/clinoptilolite: an efficient solid base in SNAr and copper-catalyzed Ullmann reactions." Canadian Journal of Chemistry 94, no. 1 (January 2016): 95–104. http://dx.doi.org/10.1139/cjc-2015-0300.

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CsF/clinoptilolite was found to be an efficient solid base catalyst for both SNAr and Ullmann ether reactions. A general and efficient one-step procedure was developed for the synthesis of biaryl ethers via direct coupling of electron-deficient aryl halides to phenols using CsF/clinoptilolite. The protocol was also applied to electron-rich aryl halides by addition of a catalytic amount of copper oxide nanoparticles. Both SNAr and Ullmann reactions were rapid and provided good to excellent yields.

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30

Li, K., and R. F. Helm. "Neolignan Skeletons and Benzodioxanes Through Chiral Aryl Alkyl Ether Formation." Holzforschung 54, no. 6 (October 25, 2000): 597–603. http://dx.doi.org/10.1515/hf.2000.101.

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Summary Several chiral neolignan skeletons and a benzodioxane were prepared from a tartrate derivative with the crucial chiral aryl alkyl ether formation being accomplished with cesium phenolate and 18-crown-6. These compounds have greater than 96% enantiomeric excess, and this work represents the first successful synthetic preparation of optically active 8-O-4′ type neolignan skeletons. The chiral aryl alkyl ethers were also synthesized from several protected carbohydrates, which can serve as chiral auxiliaries for a wide variety of target molecules.

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31

Bandar, Jeffrey, and Chaosheng Luo. "Synthesis of β-Phenethyl Ethers by Base-Catalyzed Alcohol Addition Reactions to Aryl Alkenes." Synlett 29, no. 17 (June 25, 2018): 2218–24. http://dx.doi.org/10.1055/s-0037-1610166.

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The direct anti-Markovnikov addition of alcohols to styrene derivatives represents a streamlined route to β-phenethyl ethers, a substructure frequently found in pharmaceuticals and other bioactive molecules. Here, we discuss how the development of such a reaction can complement and address limitations of current methods for β-phenethyl ether synthesis. In particular, we highlight our recent approach toward achieving this challenging alcohol addition reaction through P4-t-Bu superbase catalysis. A summary of compatible aryl alkenes and alcohols is provided to inform readers of potential applications of this new catalytic transformation, as well as its current limitations and future directions.1 Introduction2 Anti-Markovnikov Alcohol Addition to Aryl Alkenes: Background3 Superbase-Catalyzed Alcohol Addition to Aryl Alkenes4 Summary and Outlook

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32

Broxton, TJ. "Micellar Catalysis of Organic Reactions. XXXI. A Study of the Effects of Micelles of Cetyltrimethylammonium Bromide on Some SNAr Reactions in Aqueous Binary Mixtures." Australian Journal of Chemistry 44, no. 5 (1991): 667. http://dx.doi.org/10.1071/ch9910667.

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The effect of micelles of cetyltrimethylammonium bromide ( ctab ) on the SNAr reactions of 1-fluoro-2,4-dinitrobenzene (1), 2-fluoro-5-nitrobenzoate (2) and 4-fluoro-3-nitrobenzoate (3) with sodium hydroxide in aqueous binary mixtures with several alcohols has been studied. Two products were detected in all of these reactions: the phenol from reaction with hydroxide ions, and an aryl alkyl ether from reaction with the alkoxide ions. Micelles of ctab increased the percentage yield of the ether product at the expense of the phenol for compounds (1) and (2) in most of the binary mixtures used. For compound (3), however, micelles of ctab had little effect on the product distribution. These differences were attributed to differences in the orientation of substrates (2) and (3) when solubilized by micelles of ctab . Very high yields of the ether were obtained for the reaction of compound (1) with hydroxide ions in trifluoroethanol /water mixtures, and this was attributed to the considerable ionization of trifluoroethanol which was the most acidic alcohol used in this work. The lowest yield of the ether product was obtained in reactions of compound (1) with hydroxide ions in propan-2-ol/water mixtures since propan-2-ol was the least acidic alcohol used. These results are compared with those previously reported for the reaction of compound (1) in the presence of hydroxy-functionalized micelles and β- cyclodextrin. In the presence of micelles of ctab the aryl alkyl ethers derived from compounds (1) and (2) underwent a subsequent SNAr reaction with hydroxide ions during which the alkoxide ion was displaced. For compound (3) no subsequent reaction of the ether was detected in the presence of micelles of ctab . This was also attributed to the orientation of this product within the micelle. The reaction centre was buried in the micellar interior, and hence was shielded from a subsequent reaction. The rates of this subsequent reaction for compound (1), and of the decomposition of micellar aryl ethers and of cyclodextrin aryl ethers derived from compound (1), are also compared. The increase in the yield of the ether product in the presence of micelles was attributed to the increased ionization of alcohols in the presence of cationic micelles.

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33

Li, Shuai, Xia Wang, Xin-Ge Yang, Gui-Quan Yu, and Xue-Qiang Wang. "Deuterated Aryl Alkyl Ethers Synthesis via Nucleophilic Etherification of Aryl Alkyl Ethers and Thioethers with Deuterated Alcohols." Synlett 30, no. 15 (August 15, 2019): 1805–9. http://dx.doi.org/10.1055/s-0037-1611898.

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A transition-metal-free etherification protocol that is capable of synthesizing deuterated ethers is described. A wide range of aryl alkyl ethers and thioethers were suitable for this transformation owing to the mild reaction conditions. Besides, a series of sterically bulky deuterated alcohols were successfully incorporated into cyano-substituted arenes. The results of mechanistic studies suggested this reaction might take place via nucleophilic aromatic substitution pathway.

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34

Ankala, Sudha V., and Gabriel Fenteany. "ChemInform Abstract: Selective Deprotection of Either Alkyl or Aryl Silyl Ethers from Aryl, Alkyl Bis-silyl Ethers." ChemInform 33, no. 41 (May 19, 2010): no. http://dx.doi.org/10.1002/chin.200241069.

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35

Lissel, Manfred, Jürgen Kottmann, Dov Tamarkin, and Mordechai Rabinovitz. "Reductive Cleavage of Aryl-O-and Aryl-CI- Bonds by C8K: a Potential Method for the Degradation of Dioxins." Zeitschrift für Naturforschung B 43, no. 9 (September 1, 1988): 1211–12. http://dx.doi.org/10.1515/znb-1988-0922.

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36

Alonso-Marañón, Lorena, M. Montserrat Martínez, Luis A. Sarandeses, and José Pérez Sestelo. "Indium-catalyzed intramolecular hydroarylation of aryl propargyl ethers." Organic & Biomolecular Chemistry 13, no. 2 (2015): 379–87. http://dx.doi.org/10.1039/c4ob02033b.

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37

Heravi, Majid M., Farhad Panahi, and Nasser Iranpoor. "Nickel-catalyzed reductive amidation of aryl-triazine ethers." Chemical Communications 56, no. 13 (2020): 1992–95. http://dx.doi.org/10.1039/c9cc08727c.

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38

ORIYAMA, T., K. NODA, and K. YATABE. "ChemInform Abstract: Highly Efficient and Convenient Methods for the Direct Conversion of Aryl Silyl Ethers and Aryl Acetates into Aryl Alkyl Ethers." ChemInform 28, no. 48 (August 2, 2010): no. http://dx.doi.org/10.1002/chin.199748113.

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39

Seto, Chika, Takeshi Otsuka, Yoshiki Takeuchi, Daichi Tabuchi, and Takashi Nagano. "Iron-Catalyzed Grignard Cross-Couplings with Allylic Methyl Ethers or Allylic Trimethylsilyl Ethers." Synlett 29, no. 09 (March 19, 2018): 1211–14. http://dx.doi.org/10.1055/s-0036-1591774.

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We have found that cross-coupling between aryl Grignard reagents and allylic methyl ethers proceeded well in the presence of a catalytic amounts of Fe(acac)3 to afford the corresponding allylic substitution products in good yields. Under the same conditions, allylic trimethylsilyl ethers also reacted with Grignard reagents to give the corresponding cross-coupling products.

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40

Li, Guangzhe, Mieko Arisawa, and Masahiko Yamaguchi. "Rhodium-catalyzed synthesis of unsymmetrical di(aryl/heteroaryl)methanes using aryl/heteroarylmethyl ketones via CO–C bond cleavage." Chem. Commun. 50, no. 33 (2014): 4328–30. http://dx.doi.org/10.1039/c4cc00816b.

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41

Pethő, Bálint, Dóra Vangel, János T. Csenki, Márton Zwillinger, and Zoltán Novák. "Palladium catalyzed chloroethoxylation of aromatic and heteroaromatic chlorides: an orthogonal functionalization of a chloroethoxy linker." Organic & Biomolecular Chemistry 16, no. 26 (2018): 4895–99. http://dx.doi.org/10.1039/c8ob01146j.

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42

Xu, Huanjun, Bo Yu, Hongye Zhang, Yanfei Zhao, Zhenzhen Yang, Jilei Xu, Buxing Han, and Zhimin Liu. "Reductive cleavage of inert aryl C–O bonds to produce arenes." Chemical Communications 51, no. 61 (2015): 12212–15. http://dx.doi.org/10.1039/c5cc03563e.

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43

M. Downie, Ian, Harry Heaney, and Graham Kemp. "Preparation of alkyl-aryl ethers and thioethers." Tetrahedron 44, no. 9 (January 1988): 2619–24. http://dx.doi.org/10.1016/s0040-4020(01)81713-0.

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44

Godfrey, Jollie D., Richard H. Mueller, Thomas C. Sedergran, Nachimuthu Soundararajan, and Vincent J. Colandrea. "Improved synthesis of aryl 1,1-dimethylpropargyl ethers." Tetrahedron Letters 35, no. 35 (August 1994): 6405–8. http://dx.doi.org/10.1016/s0040-4039(00)78231-1.

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45

FUKUI, Hiroyuki, Hiroshi MURATA, Ken-ichi SANECHIKA, and Masanori IKEDA. "Improved Antiwear Effectiveness by Aryl Fluoroalkyl Ethers." NIPPON KAGAKU KAISHI, no. 9 (2001): 517–22. http://dx.doi.org/10.1246/nikkashi.2001.517.

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Kirsch, Stefan F., Larry E. Overman, and Nicole S. White. "Catalytic Asymmetric Synthesis of Allylic Aryl Ethers." Organic Letters 9, no. 5 (March 2007): 911–13. http://dx.doi.org/10.1021/ol070110b.

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Toerincsi, Mercedes, Pal Kolonits, Jenoe Fekete, and Lajos Novak. "ChemInform Abstract: Rearrangement of Aryl Geranyl Ethers." ChemInform 44, no. 1 (January 1, 2013): no. http://dx.doi.org/10.1002/chin.201301034.

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Chung, Hyun-A., Jeum-Jong Kim, Ho-Kyun Kim, Deok-Heon Kweon, Sang-Gyeong Lee, Yong-Jin Yoon, and Su-Dong Cho. "Synthesis of alkyl or aryl pyridazinyl ethers." Journal of Heterocyclic Chemistry 42, no. 4 (May 2005): 639–46. http://dx.doi.org/10.1002/jhet.5570420425.

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Sergeev, A. G., and J. F. Hartwig. "Selective, Nickel-Catalyzed Hydrogenolysis of Aryl Ethers." Science 332, no. 6028 (April 21, 2011): 439–43. http://dx.doi.org/10.1126/science.1200437.

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Moss, Robert A., Lei Wang, Christina M. Odorisio, Min Zhang, and Karsten Krogh-Jespersen. "Solvation of Dichlorocarbene: Complexation with Aryl Ethers." Journal of Physical Chemistry A 114, no. 1 (January 14, 2010): 209–17. http://dx.doi.org/10.1021/jp9075542.

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