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Journal articles on the topic '4-methoxyphenoxo'

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Published: 5 June 2025

Last updated: 1 August 2025

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1

K., C. MALHOTRA, SHARMA NEERAJ, S. BHATT S., and C. CHAUDIIRY S. "Preparation and Characterisation of Trichloromono (4-methoxyphenoxo ) titanium(IV)." Journal of Indian Chemical Society Vol. 71, March 1994 (1994): 139–41. https://doi.org/10.5281/zenodo.5894028.

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Department of Chemistry, Himachal Pradesh University, Summer Hill, Shimla-171 005 <em>Manuscript received 21 September 1992, reVIsed 17 February 1993, accepted 14 May 1993</em> Preparation and Characterisation of Trichloromono (4-methoxyphenoxo ) titanium(IV)

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2

Chaudhry, S. C., Anup Kumar, S. S. Bhatt, and Neeraj Sharma. "Synthesis and Reactions of Tetrakis(4-Methoxyphenoxo)titanium(IV)." Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry 22, no. 1 (1992): 1–9. http://dx.doi.org/10.1080/15533179208020635.

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3

S.C., Chaudhry, Bandna Kumari, S. Bhatt S., and Sharma Neeraj. "Synthesis, characterization and reactivity of dichloro bis(4-methoxyphenoxo)tin(IV)." Journal of Indian Chemical Society Vol. 86, Jun 2009 (2009): 633–39. https://doi.org/10.5281/zenodo.5811821.

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Department of Chemistry, Himachal Pradesh University, Summer Hill, Shimla- 171 005, Himachal Pradesh, India <em>E-mail :</em> scchaudhry@sancharnet.in <em>Manuscript received 2 September 2008, accepted 26 February 2009</em> The dichloro bis(4-methoxyphenoxo)tin(IV) complex of composition SnCI<sub>2</sub>(OC<sub>6</sub>H<sub>4</sub>OMe-4)<sub>2</sub> has been synthesized In quantitative yield by the reaction of tin tetrachloride with bimolar amount of 4-methoxyphenol in benzene under reflux and characterized by elemental analyses, molar conductance measurement

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4

Sharma, Neeraj, Anoop K. Sood, S. S. Bhatt, and S. C. Chaudhry. "4-methoxyphenoxo complexes of monooxovanadium(V) and their reactions with cyanoanilines and cyanopyridines." Polyhedron 16, no. 23 (1997): 4055–60. http://dx.doi.org/10.1016/s0277-5387(97)00173-3.

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5

Nasir, Shah Bakhtiar, Zanariah Abdullah, Azizah Mainal, Zainal A. Fairuz, Seik Weng Ng, and Edward R. T. Tiekink. "2-(4-Methoxyphenoxy)pyrazine." Acta Crystallographica Section E Structure Reports Online 66, no. 9 (2010): o2303. http://dx.doi.org/10.1107/s1600536810031946.

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6

Liu, Gang, and Jie Gao. "2-(4-Methoxyphenoxy)acetohydrazide." Acta Crystallographica Section E Structure Reports Online 68, no. 6 (2012): o1969. http://dx.doi.org/10.1107/s160053681202435x.

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The title compound, C9H12N2O3, was synthesized by the reaction of ethyl 2-(4-methoxyphenoxy)acetate with hydrazine hydrate in ethanol. In the acetohydrazide group, the N—N bond is relatively short [1.413 (2) Å], suggesting some degree of electronic delocalization in the molecule. In the crystal, molecules are linked into sheets lying parallel to the ab plane by N—H...N and N—H...O hydrogen bonds.

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7

A~gar, Ayşen, and Nazan Ocak Ískeleli. "4-(2-Methoxyphenoxy)phthalonitrile." Acta Crystallographica Section E Structure Reports Online 63, no. 2 (2007): o712—o713. http://dx.doi.org/10.1107/s1600536807001055.

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8

Heilmann-Brohl, Julia, Gérard Jaouen, and Michael Bolte. "4-(3-Methoxyphenoxy)butyric acid." Acta Crystallographica Section E Structure Reports Online 65, no. 4 (2009): o778. http://dx.doi.org/10.1107/s1600536809008186.

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9

Nasir, Shah Bakhtiar, Zanariah Abdullah, Zainal A. Fairuz, Seik Weng Ng, and Edward R. T. Tiekink. "2-(4-Methoxyphenoxy)-3-nitropyridine." Acta Crystallographica Section E Structure Reports Online 66, no. 9 (2010): o2428. http://dx.doi.org/10.1107/s1600536810034057.

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10

Yu, Lijuan, Xiaole Zhou, Yinghui Yin, Renjie Li, and Tianyou Peng. "4,5-Bis(4-methoxyphenoxy)phthalonitrile." Acta Crystallographica Section E Structure Reports Online 66, no. 10 (2010): o2527. http://dx.doi.org/10.1107/s1600536810035610.

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11

Ji, Jun, XiuQin Zhang, Kai Wang, ChaoFan Ju, and Qiang Chen. "1,2-Bis(4-methoxyphenoxy)ethane." Acta Crystallographica Section E Structure Reports Online 69, no. 4 (2013): o547. http://dx.doi.org/10.1107/s1600536813007009.

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12

Schäfer, Andreas, Ljuba Iovkova-Berends, Stefan Gilke, Paul Kossmann, Hans Preut, and Martin Hiersemann. "Crystal structure of 4-(4-methoxyphenoxy)benzaldehyde." Acta Crystallographica Section E Crystallographic Communications 71, no. 12 (2015): o1021. http://dx.doi.org/10.1107/s2056989015022707.

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The title compound, C14H12O3, was synthesizedviathe nucleophilic addition of 4-methoxyphenol to 4-fluorobenzaldehyde. The dihedral angle between the least-squares planes of the benzene rings is 71.52 (3)° and the C—O—C angle at the central O atom is 118.82 (8)°. In the crystal, weak C—H...O hydrogen bonds link the molecules to generate supramolecular layers in thebcplane. The layers are linked by weak C—H...π interactions.

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13

Duan, Zhong-Yu, and Wen-Jun Zhang. "4-[4-(4-Formyl-2-methoxyphenoxy)butoxy]-3-methoxybenzaldehyde." Acta Crystallographica Section E Structure Reports Online 61, no. 10 (2005): o3355—o3356. http://dx.doi.org/10.1107/s160053680502951x.

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14

Kartal, Aslı, Çiğdem Albayrak, Ayşen Ağar, Nazan Ocak Ískeleli, and Ahmet Erdönmez. "4-(4-Acetyl-2-methoxyphenoxy)benzene-1,2-dicarbonitrile." Acta Crystallographica Section E Structure Reports Online 62, no. 7 (2006): o2720—o2721. http://dx.doi.org/10.1107/s1600536806020204.

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15

Şahin, Onur, Orhan Büyükgüngör, Selami Şaşmaz, and Cihan Kantar. "4-(4-Allyl-2-methoxyphenoxy)benzene-1,2-dicarbonitrile." Acta Crystallographica Section E Structure Reports Online 63, no. 11 (2007): o4205. http://dx.doi.org/10.1107/s1600536807045138.

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In the title compound, C18H14N2O2, the dihedral angle between the two benzene rings is 88.6 (1)°. The allyl group is disordered over two orientations, with refined occupancies of 0.695 (6) and 0.305 (6). The methoxy group is coplanar with the attached benzene ring. C—H...N intermolecular hydrogen bonds link the molecules into a C(6) chain along the a axis. The chain structure is further strengthened by C—H...π interactions.

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16

HAN, Young-Hoon, Kwang-Soo SHIN, Hong-Duk YOUN, Yung Chil HAH, and Sa-Ouk KANG. "Mode of action and active site of an extracellular peroxidase from Pleurotus ostreatus." Biochemical Journal 314, no. 2 (1996): 421–26. http://dx.doi.org/10.1042/bj3140421.

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The properties of the haem environment of an extracellular peroxidase from Pleurotus ostreatus were studied by electronic absorption spectroscopy. A high-spin ferric form was predominant in the native enzyme and a high-spin ferrous form in the reduced enzyme. Cyanide was readily bound to the haem iron in the native form, thereby changing the enzyme to a low-spin cyano adduct. The electronic absorption spectra of the enzyme were similar to those of lignin peroxidase from Phanerochaete chrysosporium. Compound III of the enzyme was formed after the addition of an excess of H2O2 to the native enzy

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17

Shen, Lei, Yong-Hong Hu, Wen-Ge Yang, Xiao-Lei Zhao, and Jin-Feng Yao. "1-Bromo-2-(4-methoxyphenoxy)ethane." Acta Crystallographica Section E Structure Reports Online 66, no. 2 (2010): o439. http://dx.doi.org/10.1107/s1600536810001893.

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18

Shang, Zhen-Hua, Hai-Jun Lv, and Jin-Long Gao. "N-[2-(4-Methoxyphenoxy)ethyl]acetamide." Acta Crystallographica Section E Structure Reports Online 63, no. 6 (2007): o2959. http://dx.doi.org/10.1107/s1600536807022726.

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19

Barlin, GB, LP Davies, SJ Ireland, CLY Khoo, and TMT Nguyen. "Imidazo[1,2-B]pyridazines. IX. Syntheses and Central Nervous System Activities of Some 3-Alkoxy-6-(o-alkoxy, o-methylthio- or o-fluoro-phenoxy)-2-arylimidazo[1,2-b]pyridazines." Australian Journal of Chemistry 43, no. 3 (1990): 503. http://dx.doi.org/10.1071/ch9900503.

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Syntheses are reported for a series of 6-(o-methoxy -, o-ethoxy -, o-methylthio - and o-fluoro-phenoxy )-3-( methoxy and ethoxy )-2- phenyl(substituted phenyl and pyridin-3″-yl) imidazo [1,2-b] pyridazines . IC50 values are reported for the displacement of 3H-diazepam from rat brain membrane by each of these compounds. The most active compounds were found to be 3-ethoxy-2-(p- fluorophenyl )-6-(o- methoxyphenoxy )-, 3-methoxy-6-(o- methoxyphenoxy )-2-(m-nitrophenyl )- and 3-methoxy-6-(o- methoxyphenoxy )-2-(3″,4″-methylenedioxy ) imidazo [1,2-b] pyridazines with IC5O values of 15, 18 and 19 nM

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20

Diao, Chun-Hua, Min-Jie Guo, Ming Yu, Xin Chen, and Zuo-Liang Jing. "4-[6-(4-Formyl-2-methoxyphenoxy)hexyloxy]-3-methoxybenzaldehyde." Acta Crystallographica Section E Structure Reports Online 61, no. 11 (2005): o3670—o3671. http://dx.doi.org/10.1107/s1600536805032253.

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21

Diao, Chun-Hua, Min-Jie Guo, Ming Yu, Xin Chen, Zuo-Liang Jing, and Qi-Liang Deng. "4-[2-(4-Formyl-2-methoxyphenoxy)ethoxy]-3-methoxybenzaldehyde." Acta Crystallographica Section E Structure Reports Online 61, no. 11 (2005): o3741—o3742. http://dx.doi.org/10.1107/s1600536805032861.

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22

Han, Jian-Rong, and Xiao-Li Zhen. "3-[4-(5-Formyl-2-methoxyphenoxy)butoxy]-4-methoxybenzaldehyde." Acta Crystallographica Section E Structure Reports Online 61, no. 12 (2005): o4049—o4050. http://dx.doi.org/10.1107/s1600536805036135.

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23

Erzunov, Dmitry, Anastasia Rassolova, Igor Abramov, Vladimir Maizlish, Roman Rumyantsev, and Arthur Vashurin. "Crystal Structure of 5-Nitro-4-(4-methoxyphenoxy)phthalonitrile." Molbank 2025, no. 1 (2025): M1946. https://doi.org/10.3390/m1946.

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This article presents findings on the synthesis and crystal structure analysis of 5-nitro-4-(4-methoxyphenoxy)phthalonitrile. The crystal structure was meticulously refined using X-ray diffraction techniques, which allowed for a detailed examination of the molecular arrangement within the crystal. The manuscript elaborates on the significant intermolecular and intramolecular interactions that contribute to the overall crystal packing, highlighting how these interactions influence the stability and properties of the material.

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24

Ismaeel yaseen majeed. "الرابط بين طريقة ديراك وطريقة هاملتون-جاكوبي للأنظمة المقيدة من الدرجة الثانية". Journal of the College of Basic Education 19, № 79 (2022): 695–715. http://dx.doi.org/10.35950/cbej.v19i79.7366.

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تم تحويل الفانيلين إلى ethyl-2- (4-formyl-2-methoxyphenoxy) acetate (A1) عن طريق تفاعل الفانيلين مع ethylchloroacetate في وسط قاعدي في أسيتون جاف.تم تصنيع 2 - ((4-hydazonomethyl) -2-methoxyphenoxy) acetohydrazide (A2) عن طريق تفاعل (A1) مع هيدرات الهيدرازين ، أعطى الإيثانول المطلق مركب هيدرازيد ، من الهيدرازيد قمنا بتصنيع سلسلة من المركبات (Oxadiazole ، Triazole ، Aziridine ، قواعد شيف والمركبات المشتقة الأخرى).تم التعرف على هذه المركبات بواسطة TLC (كروماتوغرافيا الطبقة الرقيقة). ، MP (نقطة الانصهار). ، FT (تحويل فورييه) ، IR ، H-NMR والتحليل الأولي (CHNS).

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25

Niu, Yanyan, and Bo Wu. "4-(5-Hydroxymethyl-2-methoxyphenoxy)benzoic acid." Acta Crystallographica Section E Structure Reports Online 67, no. 5 (2011): o1069. http://dx.doi.org/10.1107/s1600536811012190.

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26

Zhang, Tao, Wenjing Wang, Jiao Xu, Liwei Ni, and Xing Zhang. "3,4-Bis[4-(4-methoxyphenoxy)phenyl]-2,5-dihydrofuran-2,5-dione." Acta Crystallographica Section E Structure Reports Online 67, no. 6 (2011): o1288. http://dx.doi.org/10.1107/s1600536811015509.

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27

Erdem, Talip Kaya, Şehriman Atalay, Nesuhi Akdemir, Erbil Agˇar, and Cihan Kantar. "4-(2-Benzoyl-5-methoxyphenoxy)benzene-1,2-dicarbonitrile." Acta Crystallographica Section E Structure Reports Online 61, no. 5 (2005): o1429—o1431. http://dx.doi.org/10.1107/s1600536805011918.

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28

Hu, T. Q., G. Leary та D. Wong. "A New Approach Towards the Yellowing Inhibition of Mechanical Pulps. Part I: Selective Removal of α-Hydroxyl and α-Carbonyl Groups in Lignin Model Compounds". Holzforschung 53, № 1 (1999): 43–48. http://dx.doi.org/10.1515/hf.1999.008.

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Summary The α-hydroxyl group in lignin model compounds 1-(3,4-dimethoxyphenyl)-2-(2-methoxyphenoxy)-1,3-propanediol (1) and 1-(4-hydroxy-3-methoxyphenyl)ethanol (3), and the α-carbonyl group in 1-(3,4-dimethoxyphenyl)-2-(2-methoxyphenoxy)ethan-1-one (5) are removed by treatment of the model compounds with trifluoroacetic acid (CF3CO OH) and triethylsilane (Et3sih) in methylene chloride. The reaction is highly chemoselective and it tolerates the lignin γ-hydroxyl group, phenol and β-O-4-aryl ether linkage. The α-hydroxyl group in 1 has also been removed with triethylsilane in aqueous trifluoroa

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29

Qi, Ai-Di, Qing-Hua Zhu, Yong-Zhi He, and Xiao-Liang Ren. "4-{2-[2-(4-Formyl-2-methoxyphenoxy)ethoxy]ethoxy}-3-methoxybenzaldehyde." Acta Crystallographica Section E Structure Reports Online 61, no. 11 (2005): o3784—o3785. http://dx.doi.org/10.1107/s1600536805033283.

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30

Tengler, Jan, Iva Kapustíková, Matúš Peško, et al. "Synthesis and Biological Evaluation of 2-Hydroxy-3-[(2-aryloxyethyl)amino]propyl 4-[(Alkoxycarbonyl)amino]benzoates." Scientific World Journal 2013 (2013): 1–13. http://dx.doi.org/10.1155/2013/274570.

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A series of twenty substituted 2-hydroxy-3-[(2-aryloxyethyl)amino]propyl 4-[(alkoxycarbonyl)amino]benzoates were prepared and characterized. As similar compounds have been described as potential antimycobacterials, primaryin vitroscreening of the synthesized carbamates was also performed against two mycobacterial species. 2-Hydroxy-3-[2-(2,6-dimethoxyphenoxy)ethylamino]-propyl 4-(butoxycarbonylamino)benzoate hydrochloride, 2-hydroxy-3-[2-(4-methoxyphenoxy)ethylamino]-propyl 4-(butoxycarbonylamino)benzoate hydrochloride, and 2-hydroxy-3-[2-(2-methoxyphenoxy)ethylamino]-propyl 4-(butoxycarbonyla

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31

Arshad, Muhammad Nadeem, Scott T. Mough, John C. Goeltz, and K. Travis Holman. "Methyl 3,5-bis[(4-hydroxymethyl-2-methoxyphenoxy)methyl]benzoate." Acta Crystallographica Section E Structure Reports Online 66, no. 3 (2010): o703. http://dx.doi.org/10.1107/s160053681000677x.

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32

Han, Jian-Rong, and Xiao-Li Zhen. "3-[2-(5-Formyl-2-methoxyphenoxy)ethoxy]-4-methoxybenzaldehyde." Acta Crystallographica Section E Structure Reports Online 61, no. 11 (2005): o3946—o3947. http://dx.doi.org/10.1107/s1600536805035117.

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33

Diao, Chun-Hua, Zhi Fan, Ming Yu, Xin Chen, and Zuo-Liang Jing. "2-[4-(2-Formyl-6-methoxyphenoxy)butoxy]-3-methoxybenzaldehyde." Acta Crystallographica Section E Structure Reports Online 61, no. 12 (2005): o4067—o4068. http://dx.doi.org/10.1107/s1600536805036317.

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34

Stomberg, R., W. Ibrahim, S. Li, K. Lundquist, and U. Westermark. "(Z)-2-(2-Methoxyphenoxy)-3-(4-methoxyphenyl)propenoic acid." Acta Crystallographica Section C Crystal Structure Communications 50, no. 12 (1994): 2019–22. http://dx.doi.org/10.1107/s010827019400329x.

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35

Han, Jian-Rong, and Xiao-Li Zhen. "3-[6-(5-Formyl-2-methoxyphenoxy)hexyloxy]-4-methoxybenzaldehyde." Acta Crystallographica Section E Structure Reports Online 62, no. 2 (2006): o432—o433. http://dx.doi.org/10.1107/s1600536805042716.

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36

Huang, Nian-Yu, Ming-Wu Ding, Zai-Gang Luo, Na Zuo, Xiao-Hua Zeng, and Hong-Wu He. "2-(4-Methoxyphenoxy)-1,9-diphenyl-1,9-dihydropurin-6-one." Acta Crystallographica Section E Structure Reports Online 62, no. 3 (2006): o1022—o1024. http://dx.doi.org/10.1107/s1600536806002765.

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37

Ma, Weili, Gang Chen, Wenjing Wang, and Zhenting Du. "3,4-Bis[4-(4-methoxyphenoxy)phenyl]-1-methyl-1H-pyrrole-2,5-dione." Acta Crystallographica Section E Structure Reports Online 67, no. 9 (2011): o2366. http://dx.doi.org/10.1107/s1600536811032594.

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38

Petrov, O. A., A. A. Maksimova, A. E. Rassolova, G. A. Gamov, and E. E. Maizlish. "Reactivity of Tetraphenoxy-Substituted Phthalocyanines in Acid–Base Reactions with Organic Bases." Журнал физической химии 97, no. 9 (2023): 1290–96. http://dx.doi.org/10.31857/s0044453723090157.

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The interaction of tetra-4-(2-methoxyphenoxy)phthalocyanine and tetra-4-(3-methoxyphenoxy)phthalocyanine with pyridine, 2-methylpyridine, morpholine, piperidine, n-butylamine, tert-butylamine, diethylamine, and triethylamine in benzene has been studied. The acid–base reaction involving n-butylamine and piperidine is an unusually slow process, leading to the formation of kinetically stable proton transfer complexes. The structure of these complexes is proposed. The change in the reactivity of tetraphenoxy-substituted phthalocyanines depending on the proton-acceptor ability and spatial structure

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39

Kaya, Betül, Weiam Hussin, Leyla Yurttaş, et al. "Design and Synthesis of New 1,3,4-Oxadiazole – Benzothiazole and Hydrazone Derivatives as Promising Chemotherapeutic Agents." Drug Research 67, no. 05 (2017): 275–82. http://dx.doi.org/10.1055/s-0042-119070.

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AbstractLooking for new cytotoxic and antimicrobial agents with improved antitumor activity, a series of hydrazide and oxadiazole derivatives were designed and synthesized using 3-methoxyphenol as starting substance. Novel N’-(arylidene)-2-(3-methoxyphenoxy)acetohydrazide derivatives (4a–f)/1-(4-substitutedphenyl)-2-[(5-[(3-methoxyphenoxy)methyl]-1,3,4-oxadiazol-2-yl)thio]ethan-1-one derivatives (6a–f)/N-(6-substitutedbenzothiazol-2-yl)-2-[(5-[(3-methoxyphenoxy)methyl]-1,3,4-oxadiazol-2-yl)thio]acetamide derivatives (7a–e) were obtained and evaluated for their in vitro antimicrobial activity a

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40

Piggott, Matthew J., and Dieter Wege. "The Synthesis of Ventilone A." Australian Journal of Chemistry 53, no. 9 (2000): 749. http://dx.doi.org/10.1071/ch00057.

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2-Amino-3,6-dimethoxy-4,5-methylenedioxybenzoic acid (12) was prepared from 1,4-dimethoxy-2,3-methylenedioxybenzene (8) via the isatin (11). The benzyne generated from (12) was intercepted with 3-acetyl-2-ethoxy-4-[(4-methoxyphenoxy)methyl]furan (4) to give the naphthol (27), which on treatment with cericammonium nitrate gave the dimethyl ether of ventilone A(29). Demethylation with boron tribromide then affordedventilone A (1).

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41

Chen, Xiao-Bao, Jing Xu, Ai-Hua Zheng, Jia-Hua Tian, and Hong Luo. "3-Isopropyl-2-(4-methoxyphenoxy)-1-benzofuro[3,2-d]pyrimidin-4(3H)-one." Acta Crystallographica Section E Structure Reports Online 65, no. 11 (2009): o2839. http://dx.doi.org/10.1107/s1600536809042925.

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42

Kumar, K. Mahesh, N. M. Mahabaleshwaraiah, O. Kotresh, S. Jeyaseelan, and H. C. Devarajegowda. "Methyl N-{4-[(4-methoxyphenoxy)methyl]-2-oxo-2H-chromen-7-yl}carbamate." Acta Crystallographica Section E Structure Reports Online 68, no. 6 (2012): o1734. http://dx.doi.org/10.1107/s160053681202048x.

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In the title compound, C19H17NO6, the dihedral angle between the 2H-chromene ring system and benzene ring is 5.34 (6)°. A short intramolecular C—H...O contact occurs. In the crystal, molecules are linked by N—H...O hydrogen bonds, generating C(8) chains propagating in [010]. The chains are linked by C—H...O interactions and the packing also exhibits π–π stacking interactions between benzene and pyran rings, with a centroid–centroid distance of 3.676 (9) Å.

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43

Tang, Ting, Lei Gao, Hong-Sheng Jia, Ya-Ming Wu, and Hong-Fei Ma. "Ethyl 1-[(4-acetyl-2-methoxyphenoxy)methyl]cyclopropane-1-carboxylate." Acta Crystallographica Section E Structure Reports Online 65, no. 2 (2009): o305. http://dx.doi.org/10.1107/s1600536809000956.

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44

Sun, Shi, Corene Canning, Kuiwu Wang, et al. "Antibacterial Activity of 2-(3’,5'-Dibromo-2'-methoxyphenoxy)-3,5-dibromophenol Isolated from Phyllospongia papyracea." Natural Product Communications 12, no. 4 (2017): 1934578X1701200. http://dx.doi.org/10.1177/1934578x1701200426.

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A principal active antimicrobial compound, 2-(3’,5'-dibromo-2'-methoxyphenoxy)-3,5-dibromophenol, was isolated from the methanol extract of Phyllospongia papyracea via bioassay-guided fractionation and isolation. The crude extract and the purified compound were assayed to determine the minimal inhibitory concentration and minimal bactericidal concentration (MBC) using the broth microdilution method. The purified compound was found to be highly active against Bacillus subtilis and Staphylococcus aureus at MIC=1 μg/mL, Campylobacter jejuni at MIC=2 μg/mL, Pseudomonas aeruginosa at MIC=4 μg/mL, a

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Hashizume, Daisuke, Hiroyuki Koshino, In-Kyoung Lee, and Ick-Dong Yoo. "2,3,5-Trichloro-4-methoxy-6-[2,3,5-trichloro-4-methoxy-6-(2,3,5,6-tetrachloro-4-methoxyphenoxy)phenoxy]phenol." Acta Crystallographica Section E Structure Reports Online 61, no. 5 (2005): o1367—o1369. http://dx.doi.org/10.1107/s1600536805011220.

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Yan, Shi-qiang, Xiao-mei Liang, Jian-jun Zhang, and Dao-quan Wang. "2-(4-Methoxyphenoxy)-6-methyl-3-oxo-3,6-dihydro-2H-pyran-4-yl benzoate." Acta Crystallographica Section E Structure Reports Online 65, no. 3 (2009): o586. http://dx.doi.org/10.1107/s1600536809004231.

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Selivanova, D. G., O. A. Maiorova, E. V. Shklyaeva, and G. G. Abashev. "Synthesis of push-pull chromophores including an N-[4-(4-methoxyphenoxy)butyl]carbazole fragment." Russian Journal of Organic Chemistry 51, no. 5 (2015): 735–39. http://dx.doi.org/10.1134/s1070428015050267.

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Ranjith, S., A. SubbiahPandi, A. D. Suresh, and K. Pitchumani. "3-Ethyl-5-(4-methoxyphenoxy)-2-(pyridin-4-yl)-3H-imidazo[4,5-b]pyridine." Acta Crystallographica Section E Structure Reports Online 67, no. 7 (2011): o1764. http://dx.doi.org/10.1107/s1600536811023543.

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Takano, Seiichi, Masaki Setoh, and Kunio Ogasawara. "Enantiocomplementary resolution of 4-hydroxy-5-(4-methoxyphenoxy)-1-pentyne using the same lipase." Tetrahedron: Asymmetry 4, no. 2 (1993): 157–60. http://dx.doi.org/10.1016/s0957-4166(00)82326-5.

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Nielsen, Flemming E., Palle Jacobsen, Anne Worsaae, Per O. G. Arkhammar, Philip Wahl, and John Bondo Hansen. "2-(4-Methoxyphenoxy)-5-nitro-N-(4-sulfamoylphenyl)benzamide activates Kir6.2/SUR1 KATP channels." Bioorganic & Medicinal Chemistry Letters 14, no. 23 (2004): 5727–30. http://dx.doi.org/10.1016/j.bmcl.2004.09.057.

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