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Journal articles on the topic 'Benzodioxole'

Author: Grafiati

Published: 4 June 2021

Last updated: 8 February 2022

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1

Pingali, Subramanya, James P. Donahue, and Florastina Payton-Stewart. "Tetrahydroberberine, a pharmacologically active naturally occurring alkaloid." Acta Crystallographica Section C Structural Chemistry 71, no. 4 (2015): 262–65. http://dx.doi.org/10.1107/s2053229615004076.

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Tetrahydroberberine (systematic name: 9,10-dimethoxy-5,8,13,13a-tetrahydro-6H-benzo[g][1,3]benzodioxolo[5,6-a]quinolizine), C20H21NO4, a widely distributed naturally occurring alkaloid, has been crystallized as a racemic mixture about an inversion center. A bent conformation of the molecule is observed, with an angle of 24.72 (5)° between the arene rings at the two ends of the reduced quinolizinium core. The intermolecular hydrogen bonds that play an apparent role in crystal packing are 1,3-benzodioxole –CH2...OCH3and –OCH3...OCH3interactions between neighboring molecules.

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2

Vidal, B., JY Conan, G. Lamaty, and J. Vardin. "Geometry of Some Strained Oxygen Ring Compounds: 1,3-Benzodioxole and 2,3-Dihydro-1,4-benzodioxin (Benzodioxan). Application to the Geometry of (6aR-cis)-3-Methoxy-6a,12a-dihydro-6h-[1,3]dioxolo-[5,6]benzofuro[3,2-C] [1]benzopyran (Pterocarpin)." Australian Journal of Chemistry 41, no. 7 (1988): 1107. http://dx.doi.org/10.1071/ch9881107.

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The geometry of benzodioxole, benzodioxan and the strained five- membered rings of pterocarpin are studied by the MNDO method. We show that in benzodioxole there is bond alternation towards a Kekule -like structure such as in indan (Mills-Nixon effect). In benzodioxole, owing to the smaller perimeter of the fused ring and enhanced strain, alternation is more pronounced than in indan . An explanation is offered for the strong distortion in ring angles in benzodioxole compared with indan. The effect of strain in benzodioxan and pterocarpin is discussed.

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3

Daliacker, Franz, Hans-Joachim Schieuter, and Petra Schneider. "Darstellung und Reaktionen von 1,3-Benzdioxol-biscarbaldehyden. Ein Beitrag zur Strukturaufklärung des Nepenthons A / Synthesis and Reactions of 1,3-Benzodioxoledicarboxaldehydes. A Contribution to the Structure Elucidation of Nepenthone-A." Zeitschrift für Naturforschung B 41, no. 10 (1986): 1273–80. http://dx.doi.org/10.1515/znb-1986-1014.

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We describe the preparation o f 1,3-Benzodioxole-5,6-dicarboxaldehyde (1d) and 1,3-Benzdioxole- 4,5-dicarboxaldehyde (3h). Under especially mild conditions also the synthesis of 4,7- Dimethoxy-1,3-benzodioxole-5,6-dicarboxaldehyde (4g) can be achieved. Its reaction with Hydroxyacetone leads to quinone 9a, which after methylation can be identified with the dim ethylether of Nepenthone-A .

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4

Chang, Franklin, Eric B. Jang, Chiou-Ling Hsu, Michael C. Ma, and Leonard Jurd. "Benzodioxole-1,3-benzodioxole derivatives and their effects on the reproductive physiology of insects." Archives of Insect Biochemistry and Physiology 27, no. 1 (1994): 39–51. http://dx.doi.org/10.1002/arch.940270106.

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5

Betz, Richard, Peter Klüfers, and Moritz M. Reichvilser. "2,2-Bis(pentafluorophenyloxy)-1,3-benzodioxole." Acta Crystallographica Section E Structure Reports Online 63, no. 9 (2007): o3769. http://dx.doi.org/10.1107/s1600536807038950.

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6

Srivastava, Shaifali, Madan M. Gupta, Ram K. Verma, and Sushil Kumar. "Determination of 1,3-Benzodioxanes in Piper mullesua by High-Performance Thin-Layer Chromatography." Journal of AOAC INTERNATIONAL 83, no. 6 (2000): 1484–88. http://dx.doi.org/10.1093/jaoac/83.6.1484.

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Abstract A new, simple, precise, and rapid high-performance thin-layer chromatographic method was developed for the determination of 6 benzodioxanes in Piper mullesua extract: 1′,3′-benzodioxole-5′-(2,4,8-triene-isobutyl nonanoate), 1′,3′-benzodioxole-5′-(2,4,12-triene-isobutyl tridecanoate), fargesin, sesamin, asarinin, 1′,3′-benzodioxole-5′-(2,4,8-triene-methyl nonanoate). The ingredients were separated on a precoated Silica Gel 60 F254 plate with a solvent system of toluene–acetone (92 + 8). The 6 benzodioxanes were well separated and easily identified in this chromatographic system. The se

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7

Yang, Jinliang, Suqing Shi, and Jun Nie. "Reasons for the yellowness of photocured samples by the benzophenone/1,3-benzodioxole photoinitiating system." New Journal of Chemistry 39, no. 7 (2015): 5453–58. http://dx.doi.org/10.1039/c5nj00575b.

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8

Ghichi, Nadir, Mohamed Amine Benaouida, Ali Benosmane, Ali Benboudiaf, and Hocine Merazig. "2-(1,3-Benzodioxol-5-yl)-1H-benzimidazole." Acta Crystallographica Section E Structure Reports Online 70, no. 2 (2014): o157. http://dx.doi.org/10.1107/s1600536814000737.

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The asymmetric unit of the title compound, C14H10N2O2, contains two independent molecules. In each molecule, the benzodioxole ring system displays an envelope conformation, with the methylene C atom located at the flap deviating by 0.081 (2) and 0.230 (2) Å from the mean plane formed by the other atoms. The dihedral angles between the benzoimidazole ring system (all atoms) and the benzodioxole benzene ring are 15.35 (6) and 10.99 (7)°. In the crystal, molecules are linked by N—H...N hydrogen bonds into chains running along the [101].

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9

Asiri, Abdullah M., Hassan M. Faidallah, Khulud F. Al-Nemari, Seik Weng Ng, and Edward R. T. Tiekink. "(2E)-2-[(2H-1,3-Benzodioxol-5-yl)methylidene]-2,3-dihydro-1H-inden-1-one." Acta Crystallographica Section E Structure Reports Online 68, no. 4 (2012): o1015. http://dx.doi.org/10.1107/s1600536812009464.

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In the title compound, C17H12O3, each of the five-membered rings in the inden-1-one and 1,3-benzodioxole residues is almost planar (r.m.s. deviations = 0.041 and 0.033 Å, respectively). A small twist about the single bond linking the two residues is evident [the C—C—C—C torsion angle = 8.7 (4)°]. Supramolecular zigzag layers propagating in theacplane are formed in the crystalviaC—H...O interactions. The layers are linkedviaπ–π interactions between the five- and six-membered rings of 1,3-benzodioxole residues [centroid–centroid distance = 3.4977 (14) Å].

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10

Qi, Xiu-Xiang, Ji-Shuan Suo, Li-Min Wang, Xiao-He Guo, and Sen-Xiang Cheng. "Ethyl 4-{5-[1-(hydroxymethyl)ethylaminocarbonyl]-1,3-benzodioxol-4-yl}-7-methoxy-3-benzodioxole-5-carboxylate." Acta Crystallographica Section E Structure Reports Online 62, no. 4 (2006): o1269—o1270. http://dx.doi.org/10.1107/s1600536806006246.

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In the title compound, C23H25NO10, the five-membered rings adopt envelope conformations and the dihedral angle between the two benzene rings is 67.1 (7)°. The crystal structure is stabilized by intramolecular N—H...O and intermolecular O—H...O hydrogen-bond interactions.

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11

Hussain, Mukhtiar, Saqib Ali, Muhammad Altaf, and Helen Stoeckli-Evans. "6-Nitro-1,3-benzodioxole-4-carbaldehyde." Acta Crystallographica Section E Structure Reports Online 62, no. 11 (2006): o5323—o5325. http://dx.doi.org/10.1107/s1600536806043972.

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12

Nishida, Yoshihiro, Masayuki Abe, Hiroshi Ohrui, and Hiroshi Meguro. "(+)-Tert-butyl-1,3-benzodioxole-4-carboxylic acid: Fluorescent chiral carboxylic acid with a 1,3-benzodioxole skeleton." Tetrahedron: Asymmetry 4, no. 7 (1993): 1431–34. http://dx.doi.org/10.1016/s0957-4166(00)80333-x.

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13

Wessig, Pablo, Robert Wawrzinek, Kristian Möllnitz, Elvira Feldbusch, and Uwe Schilde. "A new class of fluorescent dyes based on 1,3-benzodioxole and [1,3]-dioxolo[4.5-f]benzodioxole." Tetrahedron Letters 52, no. 46 (2011): 6192–95. http://dx.doi.org/10.1016/j.tetlet.2011.09.058.

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14

Maganhi, Stella H., Maurício T. Tavares, Mariana C. F. C. B. Damião, and Roberto Parise Filho. "N-[(1,3-Benzodioxol-5-yl)methyl]benzenesulfonamide: an analogue of capsaicin." Acta Crystallographica Section E Structure Reports Online 69, no. 11 (2013): o1700. http://dx.doi.org/10.1107/s1600536813028481.

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The title compound, C14H13NO4S, an analogue of capsaicin, differs from the latter by having a 1,3-benzodioxole ring rather than a 2-methoxyphenol moiety, and having a benzenesulfonamide group instead of an aliphatic amide chain. The five-membered ring is in an envelope conformation with the methylene C atom lying 0.221 (6) Å out of the plane formed by the other four atoms. The dihedral angle between the phenyl ring and the mean plane of the 1,3-benzodioxole fused-ring system is 84.65 (4)°. In the crystal, molecules aggregate into supramolecular layers in theacplane through C—H...O, N—H...O and

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15

Lenta, Bruno N., Rodolphe J. Chouna, Beate Neumann, Hans-Georg Stammler, and Norbert Sewald. "Crystal structure of obscurine: a natural product isolated from the stem bark ofB. obscura." Acta Crystallographica Section E Crystallographic Communications 71, no. 7 (2015): o457—o458. http://dx.doi.org/10.1107/s2056989015010567.

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The title compound, C24H31NO3{systematic name: (E)-3-[(1R*,2S*,4aS*,8aR*)-2-(benzo[d][1,3]dioxol-5-yl)-1,2,4a,5,6,7,8,8a-octahydronaphthalen-1-yl]-N-isobutylacrylamide}, is a natural product isolated from the stem bark ofB. obscura. It is composed of an octahydronaphthalene ring system substituted with an essentially planar benzodioxole ring system [r.m.s. deviation = 0.012 Å] and an extended isobutylacrylamide group. In the crystal, molecules are linked by N—H...O hydrogen bonds, forming chains propagating along [100]. The chains are linked by pairs of C—H...O hydrogen bonds, involving invers

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16

Meenakshi, R. "Spectral investigations, inhibition efficiency analysis and a TD-DFT study on tuning the light harvesting efficiency (LHE) of heterocyclic 5-nitro-1,3-benzodioxole as a photosensitizer for dye sensitized solar cells (DSSCs)." RSC Advances 6, no. 68 (2016): 63690–703. http://dx.doi.org/10.1039/c6ra07550a.

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17

Yin, Zhi-Gang, Heng-Yu Qian, Hu Jie, and Feng Yu-Li. "(E)-1,3-Benzodioxole-5-carbaldehyde 4-nitrophenylhydrazone." Acta Crystallographica Section E Structure Reports Online 63, no. 11 (2007): o4406. http://dx.doi.org/10.1107/s1600536807051719.

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18

Tagashira, Motoyuki, and Yasuyuki Ohtake. "A New Antioxidative 1,3-Benzodioxole fromMelissa officinalis." Planta Medica 64, no. 06 (1998): 555–58. http://dx.doi.org/10.1055/s-2006-957513.

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19

Momin, Mehbub I. K., Neil Koorbanally, Deresh Ramjugernath, and Muhammad D. Bala. "6-Hydroxy-2H-1,3-benzodioxole-5-carbaldehyde." Acta Crystallographica Section E Structure Reports Online 67, no. 10 (2011): o2681. http://dx.doi.org/10.1107/s1600536811037019.

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20

Liu, Shiji, Suqing Shi, Guangyu Hou, and Jun Nie. "Benzodioxole derivative as coinitiator for dental resin." Acta Odontologica Scandinavica 65, no. 6 (2007): 313–18. http://dx.doi.org/10.1080/00016350701742349.

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21

Deng, Rui-Xue, Wei-Yi Zhou, Xiao-Juan Deng, and Liang-Dong Sun. "5-(1H-Inden-2-yl)-1,3-benzodioxole." Acta Crystallographica Section E Structure Reports Online 64, no. 2 (2008): o492. http://dx.doi.org/10.1107/s1600536808001578.

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22

DALLACKER, F., M. HOLSCHBACH, U. HOLSCHBACH, and A. W. T. KONINGS. "ChemInform Abstract: 1,3-Benzodioxole Derivatives as Radioprotectives. Part 5. Preparation of 4- and 5-Hydroxy-1,3-benzodioxole Derivatives." ChemInform 22, no. 2 (2010): no. http://dx.doi.org/10.1002/chin.199102195.

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23

NISHIDA, Y., M. ABE, H. OHRUI, and H. MEGURO. "ChemInform Abstract: (+)-tert-Butyl-1,3-benzodioxole-4-carboxylic Acid: Fluorescent Chiral Carboxylic Acid with a 1,3-Benzodioxole Skeleton." ChemInform 24, no. 47 (2010): no. http://dx.doi.org/10.1002/chin.199347058.

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24

Peng, Wan Xi, Qiu Xue, Feng Juan Wu, Xu Zhang, and Zhong Feng Zhang. "Analysis on Health Risk of Volatile Organic Compounds of Smoked Bamboo Biomaterial by TD-GC-MS." Key Engineering Materials 467-469 (February 2011): 1697–701. http://dx.doi.org/10.4028/www.scientific.net/kem.467-469.1697.

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Smoked bamboo, which was made by bamboo in high temperature smoke, is a new indoors materials. In order to evaluate its potential health risk to human settlements, the volatile organic compounds of smoked bamboo biomaterial were adsorbed and determined by TD-GC-MS. And the main constituents of volatiles at 60°С were cyclononasiloxane, octadecamethyl-(35.14%), acetic acid(23.27%), cyclotrisiloxane, hexamethyl- (9.53%), bicyclo[4.4.0]dec-1-ene,2-isoprop yl-5-methyl-9-methylene-(7.56%), silane, 1,4-phenylenebis[trimethyl(4.32%), 1,3-benzodioxole, 5-(2-propenyl)- (3.47%), cedrol(2.75%), etc. (2) T

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25

Matos, M. Agostinha R., Clara C. S. Sousa, and Victor M. F. Morais. "Experimental and Computational Thermochemistry of 1,3-Benzodioxole Derivatives." Journal of Chemical & Engineering Data 52, no. 3 (2007): 1089–94. http://dx.doi.org/10.1021/je700035m.

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26

Micale, Nicola, Maria Zappalà, and Silvana Grasso. "Synthesis and antitumor activity of 1,3-benzodioxole derivatives." Il Farmaco 57, no. 10 (2002): 853–59. http://dx.doi.org/10.1016/s0014-827x(02)01276-4.

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27

Ugolini, Luisa, Isabella Della Noce, Paolo Trincia, Valerio Borzatta, and Sandro Palmieri. "Benzodioxole Derivatives as Negative Effectors of Plant Proteases." Journal of Agricultural and Food Chemistry 53, no. 19 (2005): 7494–501. http://dx.doi.org/10.1021/jf0580418.

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28

Jurd, Leonard. "New anti-tumor agents.1. Heterocyclic benzodioxole lactones." Journal of Heterocyclic Chemistry 33, no. 4 (1996): 1227–32. http://dx.doi.org/10.1002/jhet.5570330438.

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29

Hu, Zhi-Qiang, Lei Zheng, Chang-Jin Li, and Jun-Biao Chang. "Methyl 7-(4-chlorobenzoyloxy)-1,3-benzodioxole-5-carboxylate." Acta Crystallographica Section E Structure Reports Online 63, no. 1 (2006): o156—o157. http://dx.doi.org/10.1107/s160053680605197x.

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30

Jian, Ling-Yan, Xiao-Jing He, Ya-Xin Sun, Qing-Hua Jiang, and Xu Zhu. "(S)-(−)-5,5′-Bis(diphenylphosphino)-4,4′-bi-1,3-benzodioxole." Acta Crystallographica Section E Structure Reports Online 65, no. 5 (2009): o1153. http://dx.doi.org/10.1107/s1600536809015335.

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31

Wang, Yanfeng, Xinhui Pan, Dexiu Liu, and Hong-Xiang Lou. "6-Methoxymethoxy-7-trifluoromethyl-1,3-benzodioxole-5-carbaldehyde." Acta Crystallographica Section E Structure Reports Online 68, no. 7 (2012): o1981. http://dx.doi.org/10.1107/s1600536812022490.

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32

Wang, Bowen, Jinliang Yang, Jun Nie, and Xiaoqun Zhu. "Synthesis and photopolymerization kinetics of 2-phenyl-benzodioxole." Photochemical & Photobiological Sciences 13, no. 4 (2014): 651. http://dx.doi.org/10.1039/c3pp50343g.

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33

Zhang, Xu, Qing Zhi Ma, Zhong Feng Zhang, and Wan Xi Peng. "Study on Heat Release Behavior of Smoked Bamboo Biomass by TD-GC-MS." Key Engineering Materials 467-469 (February 2011): 1716–20. http://dx.doi.org/10.4028/www.scientific.net/kem.467-469.1716.

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Smoked bamboo has been put into mass production. However, many heat release volatiles would produce air pollution during thermoplasticization process. Therefore, the heat release behavior of smoked bamboo biomass was studied by TD-GC/MS to make full use of and prevent the pollution of the volatile materials. The main constituents were acetic acid(43.95%), cyclotrisiloxane, hexamethyl-(15.89%), octasiloxane, 1,1,3,3,5,5,7,7,9,9, 11,11,13,13,15,15-hexadecamethyl-(8.22%), 1,3-benzodioxole, 5-(2-propenyl)- (4.8%), cyclodecasiloxane, eicosamethyl-(4.51%), etc at 100°С. And the main constituents wer

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34

Srivastava, Shaifali, Madan M. Gupta, Arun K. Tripathi, and Sushil Kumar. "ChemInform Abstract: 1,3-Benzodioxole-5-(2,4,8-triene-methyl nonaoate) and 1,3-Benzodioxole-5-(2,4,8-triene-isobutyl nonaoate) from Piper mullesua." ChemInform 32, no. 20 (2001): no. http://dx.doi.org/10.1002/chin.200120212.

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35

Song, Qisheng, Michael Ma, Tsuey Ding, Joanne Ballarino, and Shuenn-Jue Wu. "Effects of a benzodioxole, J2581 (5-ethoxy-6-(4-methoxyphenyl)methyl-1,3-benzodioxole), on vitellogenesis and ovarian development of Drosophila melanogaster." Pesticide Biochemistry and Physiology 37, no. 1 (1990): 12–23. http://dx.doi.org/10.1016/0048-3575(90)90104-a.

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36

Ala, P., and D. S. C. Yang. "6-[1-(4-Ethoxyphenyl)ethyl]-5-methoxy-1,3-benzodioxole." Acta Crystallographica Section C Crystal Structure Communications 51, no. 9 (1995): 1917–19. http://dx.doi.org/10.1107/s0108270195003647.

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37

Fu, Xianshu, Zihong Ye, Lifei Mao, and Sasa Shao. "Methyl 6-bromo-7-methoxy-1,3-benzodioxole-5-carboxylate." Acta Crystallographica Section E Structure Reports Online 64, no. 8 (2008): o1417. http://dx.doi.org/10.1107/s1600536808019399.

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38

Dutta Gupta, Sayan, Ganga Balaji Rao, and Nulgulmnalli Manjunathiah Raghavendra. "Microwave-assisted green synthesis of 1, 3-benzodioxole derivatives." Green Chemistry Letters and Reviews 5, no. 4 (2012): 609–20. http://dx.doi.org/10.1080/17518253.2012.687776.

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39

Ala, P., and D. S. C. Yang. "5-Ethoxy-6-[1-(4-methoxyphenyl)ethyl]-1,3-benzodioxole." Acta Crystallographica Section C Crystal Structure Communications 50, no. 11 (1994): 1832–34. http://dx.doi.org/10.1107/s0108270194000016.

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40

Gainsford, G. J., S. J. Buckland, and B. Halton. "Spiro[1,3-benzodioxole-2,9' (10'H)-phenanthren]-10'-one." Acta Crystallographica Section C Crystal Structure Communications 46, no. 11 (1990): 2226–29. http://dx.doi.org/10.1107/s010827019000292x.

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41

Qadir, Abdul, Athar Ali, Muhammad Arif, et al. "Solvent Extraction and GC-MS Analysis of Sesame Seeds for Determination of Bioactive Antioxidant Fatty Acid/Fatty Oil Components." Drug Research 68, no. 06 (2017): 344–48. http://dx.doi.org/10.1055/s-0043-123466.

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AbstractThe seed kernels of Sesamum indicum L. (family: Pedaliaceae) were extracted with ethanol and yield of components determined by Gas Chromatography/Mass Spectrometry (GC/MS). The free radical scavenging activities of ethanolic extract against1, 1-Diphenyl-2-picrylhydrazyl (DPPH) were determined by UV spectrophotometer at 517 nm. Phytochemical screening revealed the presence of numerous bioactive compounds including steroids, phenolic, terpenoids, fatty acids and different types of ester compounds. The ethanolic extract was purified and analyzed by GC MS.The prevailing compounds found in

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42

Ezhilmuthu, Rukmani Perumal, Nagarajan Vembu, and Nagarajan Sulochana. "4-Methoxy-5-[4-(4-methoxy-1,3-benzodioxol-5-yl)perhydro-1H,3H-furo[3,4-c]furan-1-yl]-1,3-benzodioxole." Acta Crystallographica Section E Structure Reports Online 64, no. 7 (2008): o1306—o1307. http://dx.doi.org/10.1107/s1600536808018138.

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43

Ponnuchamy, Veerapandian, Jakub Sandak, and Anna Sandak. "Revealing of Supercritical Water Gasification Process of Lignin by Reactive Force Field Molecular Dynamics Simulations." Processes 9, no. 4 (2021): 714. http://dx.doi.org/10.3390/pr9040714.

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Gasification with supercritical water is an efficient process that can be used for the valorization of biomass. Lignin is the second most abundant biopolymer in biomass and its conversion is fundamental for future energy and value-added chemicals. In this paper, the supercritical water gasification process of lignin by employing reactive force field molecular dynamics simulations (ReaxFF MD) was investigated. Guaiacyl glycerol-β-guaiacyl ether (GGE) was considered as a lignin model to evaluate the reaction mechanism and identify the components at different temperatures from 1000 K to 5000 K. T

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44

Guo, Jing-jing, Bi-juan Yang, Chen-xu Jing, Duo-zhi Chen, and Xiao-jiang Hao. "Rapid Synthesis of Ismine, a Bioactive Amaryllidaceae Alkaloid." Journal of Chemical Research 41, no. 4 (2017): 202–4. http://dx.doi.org/10.3184/174751917x14894997017496.

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Ismine (6-[2-(methylamino)phenyl]-1,3-benzodioxole-5-methanol, 1), a biologically active alkaloid, has been synthesised by a rapid and simple four-step sequence. This synthesis involved a consecutive aryl–aryl and N–aryl coupling, leading to a phenanthridine derivative in a one-pot sequence, which employed a palladium catalyst and trifurylphosphine as the ligand. This synthesis gave an overall yield of 23%.

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45

Lakshmanan, D., S. Murugavel, R. Selvakumar, and M. Bakthadoss. "2-(2H-1,3-Benzodioxol-5-yl)-1,3-benzothiazole." Acta Crystallographica Section E Structure Reports Online 68, no. 4 (2012): o961. http://dx.doi.org/10.1107/s1600536812008914.

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In the title compound, C14H9O2S, the benzothiazole unit is oriented at a dihedral angle of 7.1 (1)° with respect to the benzodioxole unit. The dioxole ring adopts flattened envelope conformation with the methylene C atom at the flap. The crystal packing is stabilized by π–π interactions [centroid–centroid distances = 3.705 (1) and 3.752 (1) Å], C—H...π interactions and a short S...S contact of 3.485 (1) Å.

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46

Řezanka, Tomáš, Pavel Řezanka, and Karel Sigler. "Glycosides of benzodioxole-indole alkaloids from Narcissus having axial chirality." Phytochemistry 71, no. 2-3 (2010): 301–6. http://dx.doi.org/10.1016/j.phytochem.2009.10.016.

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Tasker, Andrew S., Bryan K. Sorensen, Hwan-Soo Jae, et al. "Potent and Selective Non-Benzodioxole-Containing Endothelin-A Receptor Antagonists." Journal of Medicinal Chemistry 40, no. 3 (1997): 322–30. http://dx.doi.org/10.1021/jm960077r.

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Micale, Nicola, Maria Zappalà, and Silvana Grasso. "Synthesis and cytotoxic activity of 1,3-benzodioxole derivatives. Note II." Il Farmaco 58, no. 5 (2003): 351–55. http://dx.doi.org/10.1016/s0014-827x(03)00053-3.

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Zheng, Lei, Boying Guo, Xiufang Zheng, Juan Chen, and Junbiao Chang. "3,4,5-Trimethoxyphenyl 4-bromo-7-methoxy-1,3-benzodioxole-5-carboxylate." Acta Crystallographica Section E Structure Reports Online 61, no. 8 (2005): o2508—o2509. http://dx.doi.org/10.1107/s1600536805021689.

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Hu, Sheng-Li, Neng-Fang She, and An-Xin Wu. "(2RS,3SR)-Diethyl 2,3-bis(1,3-benzodioxole-5-carbonyl)succinate." Acta Crystallographica Section E Structure Reports Online 61, no. 10 (2005): o3317—o3318. http://dx.doi.org/10.1107/s1600536805029144.

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