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Journal articles on the topic '2-methoxynaphthalene'

Author: Grafiati

Published: 7 June 2025

Last updated: 2 August 2025

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1

Nayak, Prakash S., Badiadka Narayana, Hemmige S. Yathirajan, Eric C. Hosten, Richard Betz, and Christopher Glidewell. "(2E)-3-(6-Methoxynaphthalen-2-yl)-1-(pyridin-3-yl)prop-2-en-1-one and its cyclocondensation product with guanidine, (4RS)-2-amino-4-(6-methoxynaphthalen-2-yl)-6-(pyridin-3-yl)-3,4-dihydropyrimidine monohydrate: two types of hydrogen-bonded sheet." Acta Crystallographica Section C Structural Chemistry 70, no. 11 (2014): 1011–16. http://dx.doi.org/10.1107/s2053229614021524.

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The structures of a chalcone and of its cyclocondensation product with guanidine are reported. In (2E)-3-(6-methoxynaphthalen-2-yl)-1-(pyridin-3-yl)prop-2-en-1-one, C19H15NO2, (I), the planes of the pyridine and naphthalene units make dihedral angles with that of the central spacer unit of 23.61 (13) and 23.57 (15)°, respectively, and a dihedral angle of 47.24 (9)° with each other. The molecules of (I) are linked into sheets by a combination of C—H...O and C—H...π(arene) hydrogen bonds. In the cyclocondensation product (4RS)-2-amino-4-(6-methoxynaphthalen-2-yl)-6-(pyridin-3-yl)-3,4-dihydropyri

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2

Tang, Chunbao. "2-Methoxynaphthalene-1-carbaldehyde." Acta Crystallographica Section E Structure Reports Online 65, no. 5 (2009): o1088. http://dx.doi.org/10.1107/s1600536809014287.

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3

Bolte, M., and C. Bauch. "2-Methoxynaphthalene at 173K." Acta Crystallographica Section C Crystal Structure Communications 54, no. 12 (1998): 1862–63. http://dx.doi.org/10.1107/s0108270198009330.

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4

Balo, C., F. Fernández, E. Lens, and C. López. "ADIPOYLATION OF 2-METHOXYNAPHTHALENE." Organic Preparations and Procedures International 29, no. 2 (1997): 201–5. http://dx.doi.org/10.1080/00304949709355184.

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5

Prince, P., F. R. Fronczek, and R. D. Gandour. "2-Acetoxy-7-methoxynaphthalene." Acta Crystallographica Section C Crystal Structure Communications 50, no. 5 (1994): 797–98. http://dx.doi.org/10.1107/s0108270193010194.

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6

Jin, Bo, Zhong-Cheng Song, Fu-Sheng Jiang, Wen-Hong Liu, and Zhi-Shan Ding. "2-Methoxynaphthalene-1,4-dione." Acta Crystallographica Section E Structure Reports Online 67, no. 4 (2011): o947. http://dx.doi.org/10.1107/s1600536811009883.

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7

Bell, KH, and LF Mccaffery. "Use of Menthyl 2-Methoxynaphthalene-1-sulfinates in the Andersen Synthesis of Optically Active Sulfoxides. Facile Cleavage by Grignard Reagents of Some Aromatic Methyl Ethers." Australian Journal of Chemistry 47, no. 10 (1994): 1925. http://dx.doi.org/10.1071/ch9941925.

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The pure crystalline diastereomers (1R,2S,5R)-menthyl (R)- and (S)-2-methoxynaphthalene-1-sulfinate (1b) have been prepared and, by reaction with Grignard reagents (the Andersen procedure), converted into optically active alkyl and aryl 2-methoxynaphthyl sulfoxides in 67-77% yields. Use of an excess of Grignard reagent results in facile O-alkyl cleavage of the methoxy group to the corresponding naphthol or a competing loss of the alkyl- or aryl- sulfinyl group to form 2-methoxynaphthalene. Pure diastereomers of menthyl 2,7- dimethoxynaphthalene-1-sulfinate (2b) and menthyl 4-methoxynaphthalene

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8

Meana-Esteban, B., C. Kvarnström, B. Geschke, J. Heinze, and A. Ivaska. "Electrochemical polymerization of 2-methoxynaphthalene." Synthetic Metals 139, no. 1 (2003): 133–43. http://dx.doi.org/10.1016/s0379-6779(03)00079-1.

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9

Kim, Sung Duk, Kyung Hee Lee, Jae Sung Lee, Young Gul Kim, and Kwang Eui Yoon. "The regioselective acylation of 2-methoxynaphthalene to 2-acetyl-6-methoxynaphthalene over zeolite beta." Journal of Molecular Catalysis A: Chemical 152, no. 1-2 (2000): 33–45. http://dx.doi.org/10.1016/s1381-1169(99)00266-6.

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10

Harvey, Gillian, and Georg Mäder. "The Shape-Selective Acylation of 2-Methoxynaphthalene, Catalyzed by Zeolites Y, Beta and ZSM-12." Collection of Czechoslovak Chemical Communications 57, no. 4 (1992): 862–68. http://dx.doi.org/10.1135/cccc19920862.

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The Friedel-Crafts acylation of 2-methoxynaphthalene (2MN) was investigated using zeolites USY, Beta and ZSM-12 as catalysts under batch conditions at 100 and 180 °C. Two ketone isomers, 1-acetyl-2-methoxynaphthalene (1AC) and 2-acetyl-6-methoxynaphthalene (2AC) were produced; the selectivity of the reaction could be influenced by the zeolite used. USY produced only the 1AC isomer whereas Beta and ZSM-12 produced both. Selective synthesis of 2AC was achieved by optimization of the reaction conditions using zeolite Beta as the catalyst. It was also observed that the 1AC ketone is unstable in co

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11

Guo, Y., J. Sun, F. Guo, Yu He, and P. Chen. "Friedel-Crafts acylation of 2-methoxynaphthalene with acetic anhydride catalyzed by phosphotungstic acid in ionic liquid." Bulgarian Chemical Communications 51, no. 2 (2019): 289–95. http://dx.doi.org/10.34049/bcc.51.2.4449.

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The Friedel-Crafts acylation of 2-methoxynaphthalene (2-MN) with acetic anhydride (AA) was carried out in the ionic liquid (IL) butylpyridinium tetrafluoroborate ([BPy]BF4) using phosphotungstic acid (H3PW12O40) as the catalyst. The [BPy]BF4-mediated 2-MN acylation displays good conversion and selectivity towards 1-acyl-2-methoxynaphthalene (1-AC-2-MN), with 70.4% conversion of 2-MN and 96.4% selectivity to 1-AC-2-MN obtained under the optimal conditions. Owing to the rearrangement of 1-AC-2-MN, 6-acyl-2-methoxynaphthalene (6-AC-2-MN) can be detected after 1 h of reaction time, with the highes

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12

Wang, Yang, Qiang Li, Xian Feng Gong, Xue Ling Zhao, and Yu Zhang. "Study on Synthesis of 2-Hydroxy-6-Naphthoic Acid from 2-Naphthol and Improve the Synthetic Process." Advanced Materials Research 634-638 (January 2013): 2044–48. http://dx.doi.org/10.4028/www.scientific.net/amr.634-638.2044.

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2-Hydroxy-6-naphthoic acid is an main raw material for the synthesis of polyaromatic ester, it was synthesized from 2-Naphthol by methoxylation, bromization, grignard reaction and demethylation before recrystallization (C2H5OH:H2O=2.8:1 m/m) with an overall yield of 78.5% and content of 99.1%. Furthermore, the results showed that the 6-bromo-2-methoxynaphthalene was prepared using Sn as reducing agent with 96.2% of the yield which is higher than 6-bromo-2-methoxynaphthalene was prepared using solid carbon dioxide and grignard reagent with 23.8% of the yield.

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13

BALO, C., F. FERNANDEZ, E. LENS, and C. LOPEZ. "ChemInform Abstract: Adipoylation of 2-Methoxynaphthalene." ChemInform 28, no. 33 (2010): no. http://dx.doi.org/10.1002/chin.199733078.

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14

Das, Purak, Achintesh Narayan Biswas, Debatra Narayan Neogi, Rupa Bhawmick, and Pinaki Bandyopadhyay. "(E)-1-[2-(Benzylsulfanyl)phenyldiazenyl]-4-methoxynaphthalene." Acta Crystallographica Section E Structure Reports Online 62, no. 12 (2006): o5536—o5538. http://dx.doi.org/10.1107/s160053680604671x.

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15

Serrano, D. P., J. M. Escola, R. Sanz, et al. "Hierarchical ZSM-5 zeolite with uniform mesopores and improved catalytic properties." New Journal of Chemistry 40, no. 5 (2016): 4206–16. http://dx.doi.org/10.1039/c5nj02856f.

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16

Chinea, Kimberly, Willian Vera, and Ajoy K. Banerjee. "Synthesis of 2-Acetyl-1,4-Dimethoxynaphthalene, A Potential Intermediate for Disubstituted Naphtho[2,3,c]pyran-5,10-dione." Natural Product Communications 9, no. 2 (2014): 1934578X1400900. http://dx.doi.org/10.1177/1934578x1400900221.

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2-Acetyl-1-hydroxynaphthalene was converted into the title compound in three steps (bromination, substitution and methylation). 1-Methoxynaphthalene on bromination, substitution and acetylation, respectively, also yielded the target compound.

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17

Xu, Wei-Ming, and Hong-Qiang He. "A Practical Synthesis of 2-Bromo-6-methoxynaphthalene." Organic Preparations and Procedures International 42, no. 1 (2010): 107–9. http://dx.doi.org/10.1080/00304940903526986.

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18

Troxler, Thomas, Brian A. Pryor, and Michael R. Topp. "Spectroscopy and dynamics of jet-cooled 2-methoxynaphthalene." Chemical Physics Letters 274, no. 1-3 (1997): 71–78. http://dx.doi.org/10.1016/s0009-2614(97)00646-5.

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19

Das, Aloke, K. K. Mahato, and Tapas Chakraborty. "Excimer formation in jet-cooled 2-methoxynaphthalene clusters." Chemical Physics Letters 341, no. 1-2 (2001): 115–21. http://dx.doi.org/10.1016/s0009-2614(01)00479-1.

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20

BALO, M. C., F. FERNANDEZ, C. GONZALEZ, E. LENS, and C. LOPEZ. "ChemInform Abstract: Succinoylation of 2-Methoxynaphthalene: A Reinvestigation." ChemInform 24, no. 29 (2010): no. http://dx.doi.org/10.1002/chin.199329097.

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21

Verevkin, Sergey P., Artemiy A. Samarov, and Sergey V. Vostrikov. "Does the Oxygen Functionality Really Improve the Thermodynamics of Reversible Hydrogen Storage with Liquid Organic Hydrogen Carriers?" Oxygen 4, no. 3 (2024): 266–84. http://dx.doi.org/10.3390/oxygen4030015.

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Liquid organic hydrogen carriers (LOHCs) are aromatic molecules that are being considered for the safe storage and release of hydrogen. The thermodynamic properties of a range of aromatic ethers were investigated using various experimental and theoretical methods to assess their suitability as LOHC materials. The absolute vapour pressures were measured for benzyl phenyl ether, dibenzyl ether and 2-methoxynaphthalene using the transpiration method. The standard molar enthalpies and entropies of vaporisation/sublimation were derived from the temperature dependence of the vapour pressures. The co

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22

Hodala, Janardhan L., Anand B. Halgeri, and Ganapati V. Shanbhag. "Enhancement in activity and shape selectivity of zeolite BEA by phosphate treatment for 2-methoxynaphthalene acylation." RSC Advances 6, no. 93 (2016): 90579–86. http://dx.doi.org/10.1039/c6ra16093j.

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Selective and green synthesis of 2-acetyl-6-methoxynaphthalene (2,6MNAC) is studied. Phosphate impregnation in smaller quantity regulates the pore of zeolite BEA. High selectivity to 2,6MNAC over BEA is due to the shape-selective property enhanced by P modification.

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23

Kikuchi, Koichi, Masato Hoshi, Yasushi Shiraishi, and Hiroshi Kokubun. "Fluorescence quenching of 9-cyanoanthracene by 2-naphthol and 2-methoxynaphthalene." Journal of Physical Chemistry 91, no. 3 (1987): 574–77. http://dx.doi.org/10.1021/j100287a017.

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24

Das, Debasish, and Soofin Cheng. "Friedel–Crafts acylation of 2-methoxynaphthalene over zeolite catalysts." Applied Catalysis A: General 201, no. 2 (2000): 159–68. http://dx.doi.org/10.1016/s0926-860x(00)00438-5.

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25

Andy, P., J. Garcia-Martinez, G. Lee, H. Gonzalez, C. W. Jones, and M. E. Davis. "Acylation of 2-Methoxynaphthalene and Isobutylbenzene over Zeolite Beta." Journal of Catalysis 192, no. 1 (2000): 215–23. http://dx.doi.org/10.1006/jcat.2000.2855.

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26

Ghichi, Nadir, Amel Djedouani, Douniazed Hannachid, et al. "Synthesis and crystal structures of two 1H-benzo[d]imidazole derivatives: DFT and anticorrosion studies, and Hirshfeld surface analysis." Acta Crystallographica Section C Structural Chemistry 79, no. 7 (2023): 292–304. http://dx.doi.org/10.1107/s2053229623005545.

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The title benzimidazole compounds, namely, 2-(4-methoxynaphthalen-1-yl)-1H-benzo[d]imidazole, C18H14N2O (I) and 2-(4-methoxynaphthalen-1-yl)-1-[(4-methoxynaphthalen-1-yl)methyl]-1H-benzo[d]imidazole ethanol monosolvate, C30H24N2O2·C2H6O (II), were synthesized by the condensation reaction of benzene-1,2-diamine with 4-methoxynaphthalene-1-carbaldehyde in the ratios 1:1 and 1:2, respectively. In I, the mean plane of the naphthalene ring system is inclined to that of the benzimidazole ring by 39.22 (8)°, while in II, the corresponding dihedral angle is 64.76 (6)°. This difference is probably infl

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27

Al Musayeib, Nawal M., Sabrin R. M. Ibrahim, Musarat Amina, Gadah A. Al Hamoud, and Gamal A. Mohamed. "Curviflorside and curviflorin, new naphthalene glycoside and flavanol from Plicosepalus curviflorus." Zeitschrift für Naturforschung C 72, no. 5-6 (2017): 197–201. http://dx.doi.org/10.1515/znc-2016-0180.

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Abstract The naphthalene glycosidecurviflorside [1,5-dihydroxy-8-methoxynaphthalene-2-O-β-D-xylopyranoside] (3) and the flavanol curviflorin [(+)-catechin-7-O-3″,4″-dihydroxybenzoate] (4), along with two known flavonoids: (+)-catechin (1) and quercetin (2) were isolated from the shoots of Plicosepalu scurviflorus Benth. (Loranthaceae) growing in Saudi Arabia and the chemical structures were elucidated by 2D-NMR spectroscopy.

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28

Troxler, T. "S1−S0Electronic Spectroscopy and ab Initio Calculations ofcis-2-Methoxynaphthalene." Journal of Physical Chemistry A 102, no. 25 (1998): 4775–87. http://dx.doi.org/10.1021/jp980487m.

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29

Xu, Wei-Ming, and Hong-Qiang He. "ChemInform Abstract: A Practical Synthesis of 2-Bromo-6-methoxynaphthalene." ChemInform 41, no. 29 (2010): no. http://dx.doi.org/10.1002/chin.201029108.

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30

Fromentin, E., J. M. Coustard, and M. Guisnet. "Acetylation of 2-methoxynaphthalene with acetic anhydride over a HBEA zeolite." Journal of Molecular Catalysis A: Chemical 159, no. 2 (2000): 377–88. http://dx.doi.org/10.1016/s1381-1169(00)00225-9.

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31

Brait, Axel, Hector Gonzalez, Patricia Andy, and Mark E. Davis. "Alkylation of 2-methoxynaphthalene with propylene oxide using titanium molecular sieves." Applied Catalysis A: General 194-195 (March 2000): 265–73. http://dx.doi.org/10.1016/s0926-860x(99)00373-7.

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32

Heinichen, H. K., and W. F. Hölderich. "Acylation of 2-Methoxynaphthalene in the Presence of Modified Zeolite HBEA." Journal of Catalysis 185, no. 2 (1999): 408–14. http://dx.doi.org/10.1006/jcat.1999.2526.

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33

Fromentin, E., J. M. Coustard, and M. Guisnet. "Mechanism of 1-Acetyl-2-methoxynaphthalene Isomerisation over a HBEA Zeolite." Journal of Catalysis 190, no. 2 (2000): 433–38. http://dx.doi.org/10.1006/jcat.1999.2762.

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34

Ankitathaikar*, Rani Madnakari Kiran Patil Priyanka Kankanwadi. "Purification Of 2-Methoxy Naphthalene by UV And IR Spectroscopic Methods." International Journal of Pharmaceutical Sciences 3, no. 4 (2025): 3182–91. https://doi.org/10.5281/zenodo.15285824.

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The objective of present work is to Purify and characterize by UV and FTIR Spectroscopic method for estimation of 2- methoxy naphthalene in marketed formulation. UV- Spectrophotometric method was developed using Alcohol (99%) as solvent. The developed method was standardized in terms of validation parameters such as simple, sensitive, linear as perICHQ2 (R1).Guidelines for estimation of 2-methoxy naphthalene in marketed Formulation this newly developed method was successfully applied for FTIR Spectrophotometric method was developed using KBr (potassium bromide) process to get insights concerni

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35

Singh, Ashok Kumar. "Synthesis and Crystallography of 1-acetoxy-3-ethoxy carbonyl-4-(4-methoxy)phenyl-7-methoxynaphthalene." Journal of Nepal Chemical Society 28 (May 24, 2013): 102–5. http://dx.doi.org/10.3126/jncs.v28i0.8115.

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1-Acetoxy-3-ethoxy carbonyl-4-(4-methoxy)phenyl-7-methoxynaphthalene (3) has been synthesized and characterized by X-ray diffraction method . The compound crystallizes in triclinic space group P-1 with cell parameter a = 7.793 (6) Å, b = 10.7428(16) Å, c = 13.306 (4) Å and Z = 2. DOI: http://dx.doi.org/10.3126/jncs.v28i0.8115 Journal of Nepal Chemical Society Vol. 28, 2011 Page: 102-105 Uploaded Date: May 24, 2013

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36

Jain, Pooja, Sourav Pal, and Vidya Avasare. "Ni(COD)2-Catalyzed ipso-Silylation of 2-Methoxynaphthalene: A Density Functional Theory Study." Organometallics 37, no. 7 (2018): 1141–49. http://dx.doi.org/10.1021/acs.organomet.8b00046.

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37

Shingare, Ganesh, Dharnidhar Mundhe, Abjal Pathan, Varun Talathi, Balaji Madje, and Jaishree Chamargore. "Design and synthesis of some new 5-6-dihydropyrimidine-2(1H)-thione derivatives as antimicrobial agents." INDIAN JOURNAL OF HETEROCYCLIC CHEMISTRY 35, no. 01 (2025): 173. https://doi.org/10.59467/ijhc.2025.35.173.

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A series of some new 5-6-dihydropyrimidine-2(1H)-thione derivatives (4a-l) was synthesized by the reaction of E-1-(6-methoxynaphthalene-2-yl)-3-(substituted phenyl)prop-2-en-1-ones with thiourea. The synthesized compounds were evaluated for their antimicrobial screening and showed good to moderate activity. Compounds feathering methoxy group at para position 4c and methyl group at meta position showed potent antibacterial activity. A moderate antifungal activity for compound 4l having methyl group at para position is observed.. KEYWORDS :Antimicrobial resistance, Microorganism, Pyrimidine, Cha

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38

Klinchan, Chayada, Rattiya Namngam, Anek Sitsongkham, and Pitak Chuawong. "Synthesis and Study of Naphthoquinones Derivatives." Applied Mechanics and Materials 855 (October 2016): 26–30. http://dx.doi.org/10.4028/www.scientific.net/amm.855.26.

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In this research, we reported the study and synthesis of naphthoquinones intermediate compounds lead to the target naphthoquinones derivatives product. Naphthoquinones derivatives have long been known to display anticancer and antimalarial activity in addition to a wide variety of other bioactivities. Moreover, it has been reported to possess antimalarial disease against Plasmodium falciparum. The naphthoquinones derivatives product (5) were synthesized by coupling with 2-(3-bromo-2,2-dimethylpropyl)-1-methoxynaphthalene (4) and methyl ketone fatty acid (3). The 2-(3-bromo-2,2-dimethylpropyl)-

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39

Bell, KH. "Chlorosulfination of Aromatic Methyl Ethers with Thionyl Chloride." Australian Journal of Chemistry 38, no. 8 (1985): 1209. http://dx.doi.org/10.1071/ch9851209.

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Aromatic sulfinyl chlorides have been prepared in high yield by direct chlorosulfination of some aromatic ethers (1,3-dimethoxybenzene, 2- methyl- and 4-chloro-1,3-dimethoxybenzene, 1,2,3-trimethoxybenzene, 1- and 2-methoxynaphthalene, 1,5-, 1,7-, 2,6- and 2,7- dimethoxynaphthalene ) with thionyl chloride alone at or below room temperature. Under the same conditions, 1,4-dimethoxynaphthalene and 1,3-dimethoxy-5-methylbenzene yield chlorinated starting materials and sulfides. 1,3,5-Trimethoxybenzene yields chlorinated starting material, sulfide, and a chlorinated disulfide. Some other ethers (e

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40

Meric, P. "Kinetics of 2-methoxynaphthalene acetylation with acetic anhydride over dealuminated HY zeolites." Journal of Molecular Catalysis A: Chemical 189, no. 2 (2002): 251–62. http://dx.doi.org/10.1016/s1381-1169(02)00348-5.

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41

Maeda, Hajime, Shoji Matsuda, and Kazuhiko Mizuno. "Regioselective photoalkylation of 2-cyano-6-methoxynaphthalene by methoxy-substituted 1,2-diarylcyclopropanes." Journal of Photochemistry and Photobiology A: Chemistry 206, no. 2-3 (2009): 129–33. http://dx.doi.org/10.1016/j.jphotochem.2009.05.026.

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42

Botella, P., A. Corma, and G. Sastre. "Al-ITQ-7, a Shape-Selective Zeolite for Acylation of 2-Methoxynaphthalene." Journal of Catalysis 197, no. 1 (2001): 81–90. http://dx.doi.org/10.1006/jcat.2000.3057.

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43

Pârvulescu, A. N., B. C. Gagea, V. I. Pârvulescu, D. De Vos, and P. A. Jacobs. "Acylation of 2-methoxynaphthalene with acetic anhydride over silica-embedded triflate catalysts." Applied Catalysis A: General 306 (June 2006): 159–64. http://dx.doi.org/10.1016/j.apcata.2006.03.042.

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44

Meana-Esteban, Beatriz, Andreas Petr, Carita Kvarnström, Ari Ivaska, and Lothar Dunsch. "Poly(2-methoxynaphthalene): A spectroelectrochemical study on a fused ring conducting polymer." Electrochimica Acta 115 (January 2014): 10–15. http://dx.doi.org/10.1016/j.electacta.2013.10.090.

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45

Chen, Ping, Wei Wang, and Yuchun Zhai. "Friedel–Crafts acylation of 2-methoxynaphthalene with acetic anhydride over Al-HMS." Journal of Porous Materials 21, no. 4 (2014): 441–48. http://dx.doi.org/10.1007/s10934-014-9790-y.

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46

Zhao, Yueqiang, Shilong Xiao, Weiwei Liu, and Zhengming Wu. "Computer Aided Solvent Scanning for the Separation of 2-Methoxynaphthene and 2-Acetyl-6-methoxynaphthalene." Journal of Chemical & Engineering Data 57, no. 1 (2011): 200–203. http://dx.doi.org/10.1021/je2009889.

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47

Selvaraj, M., K. Lee, K. S. Yoo, and T. G. Lee. "Synthesis of 2-acetyl-6-methoxynaphthalene using mesoporous /Al-MCM-41 molecular sieves." Microporous and Mesoporous Materials 81, no. 1-3 (2005): 343–55. http://dx.doi.org/10.1016/j.micromeso.2005.02.017.

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48

Meana-Esteban, B., C. Kvarnström, and A. Ivaska. "Spectroelectrochemical study on the charging reactions of electrochemically synthesized films from 2-methoxynaphthalene." Synthetic Metals 156, no. 5-6 (2006): 426–32. http://dx.doi.org/10.1016/j.synthmet.2006.01.006.

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Atla, Shashi B., Ashutosh A. Kelkar, and Raghunath V. Chaudhari. "Hydroesterification of 2-vinyl-6-methoxynaphthalene using palladium complexes containing chelating nitrogen ligands." Journal of Molecular Catalysis A: Chemical 307, no. 1-2 (2009): 134–41. http://dx.doi.org/10.1016/j.molcata.2009.03.021.

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Price, R. R., and M. Patchan. "Entrapment and release characteristics of 2-methoxynaphthalene from cylindrical microstructures formed from phospholipids." Journal of Microencapsulation 10, no. 2 (1993): 215–22. http://dx.doi.org/10.3109/02652049309104387.

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