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Journal articles on the topic 'Styrylchromones'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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1

C., Srinivas Rao, Jyotsna C., and S. Sait Shakil. "Palladium-mediated cyclization of 8-allyl-7 -hydroxy-2-styrylchrmnones towards the synthesis of 7 ,8-furano-2-styrylchromones." Journal of Indian Chemical Society Vol. 89, Sep 2012 (2012): 1283–87. https://doi.org/10.5281/zenodo.5769715.

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JNTUH, Dr. Reddy Laboratories, Hyderabad, India E-mail : chemistrycsr@gmail.com Manuscript received 17 February 2011, revised 13 December 2011, accepted 21 December 2011 A rapid, efficient and practical synthesis of 7,8-furano-2-styrylchromones by oxidation of 8-allyl-7-hydroxy-2-styrylchromones with dichlorobis(benzonitrile)palladium has been developed. This procedure is general and the products thus obtained have been characterized from their spectral data. DDQ oxidation of the same substrates, however, gave 7 ,8-pyrano-2-styrylchromone derivatives.

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2

Rocha, Sónia, Natália Aniceto, Rita C. Guedes, et al. "An In Silico and an In Vitro Inhibition Analysis of Glycogen Phosphorylase by Flavonoids, Styrylchromones, and Pyrazoles." Nutrients 14, no. 2 (2022): 306. http://dx.doi.org/10.3390/nu14020306.

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Glycogen phosphorylase (GP) is a key enzyme in the glycogenolysis pathway. GP inhibitors are currently under investigation as a new liver-targeted approach to managing type 2 diabetes mellitus (DM). The aim of the present study was to evaluate the inhibitory activity of a panel of 52 structurally related chromone derivatives; namely, flavonoids, 2-styrylchromones, 2-styrylchromone-related derivatives [2-(4-arylbuta-1,3-dien-1-yl)chromones], and 4- and 5-styrylpyrazoles against GP, using in silico and in vitro microanalysis screening systems. Several of the tested compounds showed a potent inhi

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3

Momin, Mehbub, Deresh Ramjugernath, Hafizah Chenia, and Neil A. Koorbanally. "Synthesis and Evaluation of Novel Fluorinated 2-Styrylchromones as Antibacterial Agents." Journal of Chemistry 2013 (2013): 1–13. http://dx.doi.org/10.1155/2013/436758.

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A range of fluorinated 2-styrylchromones (5a–g) of which six were new (5a–f) were prepared in three steps using the Baker-Venkataraman rearrangement along with two methoxylated derivatives (5h-i) and a methylenedioxy derivative (5j) and screened for their antibacterial activity using Gram-positive bacteria (Staphylococcus aureus, sciuri, andxylosusas well asBacillus subtilis) and Gram-negative bacteria (Escherichia coli, Pseudomonas aeruginosa, andKlebsiella pneumonia). The compounds were most effective againstB. subtilisfollowed byS. aureusand a single strain ofE. coli(ATCC 25922). Difluorina

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4

Simon, Lalitha. "IN-VITRO CYTOTOXICITY AND ANTIOXIDANT EVALUATION OF 7-AMINO-2-STYRYLCHROMONE DERIVATIVES." Asian Journal of Pharmaceutical and Clinical Research 10, no. 11 (2017): 152. http://dx.doi.org/10.22159/ajpcr.2017.v10i11.20587.

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Objective: The objective of this study was to synthesize 7-amino-2-styrylchromone derivatives and evaluate their in vitro cytotoxic and antioxidant potential.Methods: 7-amino-2-styrylchromones were synthesized from 7-amino-2-methylchromone by condensing it with various substituted aromatic aldehydes. The cytotoxicity of the synthesized molecules was assessed against two cell lines, MCF-7 and HCT-116 by 3-(4,5-dimethyl thiazol-2-yl)-2,5- diphenyl tetrazolium bromide assay. Cell cycle analysis of the most potent molecule ASC-7 was carried out. The antioxidant studies were conducted by 2,2-diphen

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5

Talhi, Oualid, Artur Silva, Abdelghani Bouchama, et al. "Diastereoselective One-Pot Tandem Synthesis of Chromenopyridodiazepinones through 1,4- and 1,6-Aza-Conjugate Additions/Heterocyclizations." Synlett 29, no. 07 (2018): 885–89. http://dx.doi.org/10.1055/s-0037-1609201.

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We report an efficient one-pot synthesis of a novel series of chromenopyridodiazepinone polyheterocycles by a catalyst-free nucleophilic addition of ethane-1,2-diamine to (E,E)-3-[3-(2-hydroxyphenyl)-3-oxoprop-1-en-1-yl]-2-styrylchromones at room temperature under mild conditions. The reaction proceeds by a tandem process involving 1,4- and 1,6-aza-conjugate additions of one amino group of ethane-1,2-diamine to the α,β-unsaturated (3-oxoprop-1-en-1-yl) and the α,β,γ,δ-diunsaturated (2-styrylchromone) carbonyl system of the precursor, followed by imine condensation of the remaining amino group

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6

Desideri, Nicoletta, Paola Mastromarino, and Cinzia Conti. "Synthesis and Evaluation of Antirhinovirus Activity of 3-Hydroxy and 3-Methoxy 2-Styrylchromones." Antiviral Chemistry and Chemotherapy 14, no. 4 (2003): 195–203. http://dx.doi.org/10.1177/095632020301400404.

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Recently, we identified 2-styrylchromones as a new class of antirhinovirus flavonoids with moderate activity against both rhinovirus groups A and B. In order to improve the antiviral effect of the first series of tested 2-styrylchromones, a hydroxy or methoxy group was introduced in position 3 of the chromone ring. Cytotoxicity and antiviral activity of the new synthesized compounds were evaluated in HeLa cell cultures infected with rhinoviruses 1B and 14, selected as representative serotypes for viral groups B and A of human rhinoviruses (HRVs), respectively. These antiviral results compared

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7

Lucas, Mariana, Marisa Freitas, Artur M. S. Silva, Eduarda Fernandes, and Daniela Ribeiro. "Styrylchromones: Biological Activities and Structure-Activity Relationship." Oxidative Medicine and Cellular Longevity 2021 (December 22, 2021): 1–47. http://dx.doi.org/10.1155/2021/2804521.

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Styrylchromones (SC) are a group of oxygen-containing heterocyclic compounds, which are characterized by the attachment of a styryl group to the chromone core. SC can be found in nature or can be chemically synthesized in the laboratory. As their presence in nature is scarce, the synthetic origin is the most common. Two types of SC are known: 2-styrylchromones and 3-styrylchromones. However, 2-styrylchromones are the most common, being more commonly found in nature and which chemical synthesis is more commonly described. A wide variety of SC has been described in the literature, with different

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8

Sankar, P. Dey, Chattopadhyay Falguni, and K. Mallik Asok. "Hypervalent iodine oxidation of flavonols and 3-hydroxy-2-styrylchromones in different alcohols." Journal of Indian Chemical Society Vol. 93, Nov 2016 (2016): 1321–24. https://doi.org/10.5281/zenodo.5639274.

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Department of Chemistry, Srikrishna College, Bagula, Nadia-741 502, West Bengal, India <em>E-mail</em> : deysp2002@yahoo.co.in Department of Chemistry, Jadavpur University, Kolkata-700 032, India <em>Manuscript received 18 May 2016, revised 08 September 2016, accepted 19 September 2016</em> Flavonols and 3-hydroxy-2-styrylchromones react with diacetoxyiodobenzene (DAIB) in different alcohols to yield addition compound. Alcohols used as solvent in the oxidation process add to the C-2 carbon of both the flavonols and 3-hydroxy-2-styrylchromones.

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9

Silva, Artur M. S., Diana C. G. A. Pinto, José A. S. Cavaleiro, Albert Levai, and Tamás Patonay. "Synthesis and reactivity of styrylchromones." Arkivoc 2004, no. 7 (2004): 106–23. http://dx.doi.org/10.3998/ark.5550190.0005.709.

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10

Gomes, Ana, Marisa Freitas, Eduarda Fernandes, and Jose L.F.C. Lima. "Biological Activities of 2-Styrylchromones." Mini-Reviews in Medicinal Chemistry 10, no. 1 (2010): 1–7. http://dx.doi.org/10.2174/138955710791112550.

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11

Cavaleiro, José A. S., José Elguero, M. Luísa Jimeno, and Artur M. S. Silva. "Synthesis of (E)-2-Styrylchromones." Chemistry Letters 20, no. 3 (1991): 445–46. http://dx.doi.org/10.1246/cl.1991.445.

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12

Addepalli, Yesu, Zhimei Yu, Jie Ji, Cheng Zou, Zhen Wang, and Yun He. "Tandem Diels–Alder/oxidation–aromatization reactions involving 2-styrylchromones and arynes." Organic & Biomolecular Chemistry 16, no. 33 (2018): 6077–85. http://dx.doi.org/10.1039/c8ob01199k.

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Transition-metal-free tandem Diels–Alder/oxidation–aromatization reactions between 2-styrylchromones and arynes have been demonstrated, providing a wide range of benzo[c]xanthone derivatives with good yields.

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13

Silva, Artur M. S., Diana C. G. A. Pinto, José A. S. Cavaleiro, Ana Martínez, Ana Castro, and José Elguero. "An Experimental NMR and Semi-Empirical Theoretical Study of the Conformation of Styrylchromones and Styryl Alkyl or Aryl Ketones (Benzylidene Ketones)." Journal of Chemical Research 2002, no. 4 (2002): 162–64. http://dx.doi.org/10.3184/030823402103171735.

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The configurations and conformations of styrylchromones and benzylidene ketones were determined by NMR spectroscopy. The cyclisation of the former to xanthones was studied showing clear differences in reactivity. These structural aspects were rationalised with the help of AM1 calculations.

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14

Filipe, Paulo, Artur M. S. Silva, Patrice Morlière, et al. "Polyhydroxylated 2-styrylchromones as potent antioxidants." Biochemical Pharmacology 67, no. 12 (2004): 2207–18. http://dx.doi.org/10.1016/j.bcp.2004.02.030.

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15

Santos, Clementina M. M., Artur M. S. Silva, and José A. S. Cavaleiro. "Synthesis of New Hydroxy-2-styrylchromones." European Journal of Organic Chemistry 2003, no. 23 (2003): 4575–85. http://dx.doi.org/10.1002/ejoc.200300468.

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16

UESAWA, YOSHIHIRO, JUNKO NAGAI, HAIXIA SHI, et al. "Quantitative Structure–Cytotoxicity Relationship of 2-Styrylchromones." Anticancer Research 39, no. 12 (2019): 6489–98. http://dx.doi.org/10.21873/anticanres.13863.

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17

Silva, Vera L. M., Artur M. S. Silva, Diana C. G. A. Pinto, José A. S. Cavaleiro, Attila Vasas, and Tamás Patonay. "Syntheses of (E)- and (Z)-3-styrylchromones." Monatshefte für Chemie - Chemical Monthly 139, no. 11 (2008): 1307–15. http://dx.doi.org/10.1007/s00706-008-0926-0.

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18

CAVALEIRO, J. A. S., J. ELGUERO, M. L. JIMENO, and A. M. S. SILVA. "ChemInform Abstract: Synthesis of E-2-Styrylchromones." ChemInform 23, no. 8 (2010): no. http://dx.doi.org/10.1002/chin.199208219.

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19

Momin, Mehbub, Deresh Ramjugernath, and Neil A. Koorbanally. "Structure elucidation of a series of fluoro-2-styrylchromones and methoxy-2-styrylchromones using 1D and 2D NMR spectroscopy." Magnetic Resonance in Chemistry 52, no. 9 (2014): 521–29. http://dx.doi.org/10.1002/mrc.4111.

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20

Rocha-Pereira, Joana, Ricardo Cunha, Diana C. G. A. Pinto, Artur M. S. Silva, and Maria São José Nascimento. "(E)-2-Styrylchromones as potential anti-norovirus agents." Bioorganic & Medicinal Chemistry 18, no. 12 (2010): 4195–201. http://dx.doi.org/10.1016/j.bmc.2010.05.006.

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21

Desideri, N., C. Conti, P. Mastromarino, and F. Mastropaolo. "Synthesis and Anti-Rhinovirus Activity of 2-Styrylchromones." Antiviral Chemistry and Chemotherapy 11, no. 6 (2000): 373–81. http://dx.doi.org/10.1177/095632020001100604.

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22

MAKRANDI, J. K., and SEEMA SEEMA. "ChemInform Abstract: A Modified Synthesis of 2-Styrylchromones." ChemInform 22, no. 41 (2010): no. http://dx.doi.org/10.1002/chin.199141158.

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23

Longevity, Oxidative Medicine and Cellular. "Retracted: Styrylchromones: Biological Activities and Structure-Activity Relationship." Oxidative Medicine and Cellular Longevity 2024 (January 9, 2024): 1. http://dx.doi.org/10.1155/2024/9810761.

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24

Rao, C. Srinivas, C. Jyotsna, and Shakil S. Sait. "ChemInform Abstract: Palladium-Mediated Cyclization of 8-Allyl-7-hydroxy-2-styrylchromones Towards the Synthesis of 7,8-Furano-2-styrylchromones." ChemInform 44, no. 32 (2013): no. http://dx.doi.org/10.1002/chin.201332157.

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25

S. Silva, Artur M., Diana C. G. A. Pinto, Hilário R. Tavares, José A. S. Cavaleiro, M. Luisa Jimeno, and José Elguero. "Novel (E)- and (Z)-2-Styrylchromones from (E, E)-2′-Hydroxycinnamylideneacetophenones – Xanthones from Daylight Photooxidative Cyclization of (E)-2-Styrylchromones." European Journal of Organic Chemistry 1998, no. 9 (1998): 2031–38. http://dx.doi.org/10.1002/(sici)1099-0690(199809)1998:9<2031::aid-ejoc2031>3.0.co;2-#.

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26

TAKAO, KOICHI, KAORI HOSHI, HIROSHI SAKAGAMI, et al. "Further Quantitative Structure–Cytotoxicity Relationship Analysis of 3-Styrylchromones." Anticancer Research 40, no. 1 (2019): 87–95. http://dx.doi.org/10.21873/anticanres.13929.

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27

Silva, Artur M., António de la Hoz, Diana C. Pinto, et al. "First Diels-AlderReactions of 3-Styrylchromones under Microwave Irradiation." Synlett, no. 10 (2003): 1415–18. http://dx.doi.org/10.1055/s-2003-40826.

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28

Pawar, Shrinivas P., Dasharath D. Kondhare, and P. K. Zubaidha. "Synthesis and evaluation of antioxidant activity of 2-styrylchromones." Medicinal Chemistry Research 22, no. 2 (2012): 753–57. http://dx.doi.org/10.1007/s00044-012-0069-z.

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29

PRICE, W. A., A. M. S. SILVA, and J. A. S. CAVALEIRO. "ChemInform Abstract: 2-Styrylchromones: Biological Action, Synthesis, and Reactivity." ChemInform 25, no. 11 (2010): no. http://dx.doi.org/10.1002/chin.199411329.

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30

SILVA, A. M. S., D. C. G. A. PINTO, H. R. TAVARES, J. A. S. CAVALEIRO, M. L. JIMENO, and J. ELGUERO. "ChemInform Abstract: Novel (E)- and (Z)-2-Styrylchromones from (E,E)-2′-Hydroxycinnamylideneacetophenones - Xanthones from Daylight Photooxidative Cyclization of (E)-2-Styrylchromones." ChemInform 29, no. 52 (2010): no. http://dx.doi.org/10.1002/chin.199852164.

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31

Surinder, Berar, Berar UrmiJa, Thakur Mandeep, C. Gupta Satish, and C. Kamboj Ramesh. "Photochemistry of 3-alkoxy chromones : Photocyclisation of 3-benzyloxy-6-chloro-2-(1' -methyl-2' -phenylvinyl)-4-oxo-4H-1-benzopyran." Journal of Indian Chemical Society Vol. 85, July 2008 (2008): 759–62. https://doi.org/10.5281/zenodo.5817225.

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Department of Chemistry, Kurukshetra University, Kurukshetra-136 119, Haryana, India E-mail : rckamboj@rediffmail.com            Fax: 91-1744-238277 Manuscript received 31 December 2007. accepted 6 May 2008 Photocyclisation of 3-benzyloxy-6-chloro-2-(11 -methyl-21 -phenylvinyl)-4-oxo-4<em>H</em>-1-benzopyran with pyrex filtered <strong>UV</strong> light to yield linear tricyclic pyranopyrone and angular fused tetracyclic compound is described. The product formation occurred via cyclisation of 1,4-biradical produced through H-abstraction by <strong>C=O</strong> gro

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32

Tanuma, Sei-ichi, Takahiro Oyama, Miwa Okazawa, et al. "A Dual Anti-Inflammatory and Anti-Proliferative 3-Styryl-chromone Derivative Synergistically Enhances the Anti-Cancer Effects of DNA-Damaging Agents on Colon Cancer Cells by Targeting HMGB1-RAGE-ERK1/2 Signaling." International Journal of Molecular Sciences 23, no. 7 (2022): 3426. http://dx.doi.org/10.3390/ijms23073426.

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The current anti-cancer treatments are not enough to eradicate tumors, and therefore, new modalities and strategies are still needed. Most tumors generate an inflammatory tumor microenvironment (TME) and maintain the niche for their development. Because of the critical role of inflammation via high-mobility group box 1 (HMGB1)–receptor for advanced glycation end-products (RAGE) signaling pathway in the TME, a novel compound possessing both anti-cancer and anti-inflammatory activities by suppressing the HMGB1-RAGE axis provides an effective strategy for cancer treatment. A recent work of our gr

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33

Lucas, M., M. Freitas, M. Zanchetta, et al. "P12-41 Cytotoxicity and anti-inflammatory potential of 2-styrylchromones." Toxicology Letters 368 (September 2022): S190—S191. http://dx.doi.org/10.1016/j.toxlet.2022.07.520.

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34

Lucas, Mariana, Marisa Freitas, Marco Zanchetta, Artur M. S. Silva, Eduarda Fernandes, and Daniela Ribeiro. "2-Styrylchromones: Cytotoxicity and Modulation of Human Neutrophils’ Oxidative Burst." Pharmaceuticals 15, no. 3 (2022): 288. http://dx.doi.org/10.3390/ph15030288.

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Neutrophils are polymorphonuclear leukocytes recruited to sites of acute inflammation, in response to pathogen invasion and tissue injury. The modulation of their activity, especially oxidative burst, may be important to control the inflammatory process. 2-Styrylchromones (2-SC) are derived from chromones and despite their recognized multiple biological activities, their anti-inflammatory and antioxidant properties are still poorly explored. Therefore, in this study, 43 structurally related 2-SC were evaluated concerning their effects on freshly isolated human neutrophils’ viability and oxidat

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35

Shelke, Kiran F., Suryakant B. Sapkal, Nana V. Shitole, Bapurao B. Shingate, and Murlidhar S. Shingare. "Microwave-Assisted Synthesis of 3-Styrylchromones in Alkaline Ionic Liquid." Bulletin of the Korean Chemical Society 30, no. 12 (2009): 2883–86. http://dx.doi.org/10.5012/bkcs.2009.30.12.2883.

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36

Zammattio, F., J. D. Brion, P. Ducrey, and G. Le Baut. "New Route to Styrylchromones via [1-(2-Hydroxybenzoyl)alkylidene]triphenylphosphoranes." Synthesis 1992, no. 04 (1992): 375–76. http://dx.doi.org/10.1055/s-1992-26115.

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37

Malafaia, Daniela, Joana L. C. Sousa, Artur M. S. Silva, and Hélio M. T. Albuquerque. "2,2’-[(1E,1’E)-{[Hexa-2,4-diyne-1,6-diylbis(oxy)]bis(2,1-phenylene)}bis(ethene-2,1-diyl)]bis(4H-chromen-4-one)." Molbank 2023, no. 2 (2023): M1621. http://dx.doi.org/10.3390/m1621.

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2-Styrylchromones (2-SCs) are interesting compounds for their biological properties as well as versatility as starting materials for further transformations. Herein, we disclose a new 2-SC derivative—2,2’-[(1E,1’E)-{[hexa-2,4-diyne-1,6-diylbis(oxy)]bis(2,1-phenylene)}bis(ethene-2,1-diyl)]bis(4H-chromen-4-one)—which is a dimeric compound formed by two units of 2-SC linked through a 1,3-diyne moiety. It was obtained in excellent yield (96%) through the copper-catalyzed homocoupling of two molecules of O-propargyl-2-SC. Its structure was unveiled by 1D (1H and 13C) and 2D (HSQC and HMBC) NMR tech

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38

Vallabhaneni, Madhavarao, Priyadarsini Pullagura, Hanumatha Rao Addanki, Subramanyam Chennamsetty, and Ranganayakulu Yenisetty. "A simple, efficient synthesis and molecular docking studies of 2-styrylchromones." Organic Communications, no. 2 (June 22, 2021): 121–32. http://dx.doi.org/10.25135/acg.oc.103.21.02.1959.

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39

Gomes, Ana, Eduarda Fernandes, M. Beatriz Q. Garcia, et al. "Cyclic voltammetric analysis of 2-styrylchromones: Relationship with the antioxidant activity." Bioorganic & Medicinal Chemistry 16, no. 17 (2008): 7939–43. http://dx.doi.org/10.1016/j.bmc.2008.07.072.

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40

Gomes, Ana, Eduarda Fernandes, Artur M. S. Silva, et al. "2-Styrylchromones: Novel strong scavengers of reactive oxygen and nitrogen species." Bioorganic & Medicinal Chemistry 15, no. 18 (2007): 6027–36. http://dx.doi.org/10.1016/j.bmc.2007.06.046.

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41

Patonay, Tamás, Attila Kiss-Szikszai, Vera M. L. Silva, et al. "Microwave-Induced Synthesis and Regio- and Stereoselective Epoxidation of 3-Styrylchromones." European Journal of Organic Chemistry 2008, no. 11 (2008): 1937–46. http://dx.doi.org/10.1002/ejoc.200701081.

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42

Fernandes, Eduarda, Félix Carvalho, Artur M. S. Silva, et al. "2-Styrylchromones As Novel Inhibitors of Xanthine Oxidase. A Structure-activity Study." Journal of Enzyme Inhibition and Medicinal Chemistry 17, no. 1 (2002): 45–48. http://dx.doi.org/10.1080/14756360290019944.

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43

Lin, Chen, Pei-Jung Lu, Chia-Ning Yang, Christopher Hulme, and Arthur Y. Shaw. "Structure–activity relationship study of growth inhibitory 2-styrylchromones against carcinoma cells." Medicinal Chemistry Research 22, no. 5 (2012): 2385–94. http://dx.doi.org/10.1007/s00044-012-0232-6.

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44

ZAMMATTIO, F., J. D. BRION, P. DUCREY, and G. LE BAUT. "ChemInform Abstract: New Route to Styrylchromones via (1-(2-Hydroxybenzoyl)alkylidene) triphenylphosphoranes." ChemInform 23, no. 33 (2010): no. http://dx.doi.org/10.1002/chin.199233188.

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45

Santos, Clementina M. M., and Artur M. S. Silva. "An Overview of 2-Styrylchromones: Natural Occurrence, Synthesis, Reactivity and Biological Properties." European Journal of Organic Chemistry 2017, no. 22 (2017): 3115–33. http://dx.doi.org/10.1002/ejoc.201700003.

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46

Sousa, Joana L. C., Hélio M. T. Albuquerque, and Artur M. S. Silva. "Drug Discovery Based on Oxygen and Nitrogen (Non-)Heterocyclic Compounds Developed @LAQV–REQUIMTE/Aveiro." Pharmaceuticals 16, no. 12 (2023): 1668. http://dx.doi.org/10.3390/ph16121668.

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Artur Silva’s research group has a long history in the field of medicinal chemistry. The development of new synthetic methods for oxygen (mostly polyphenols, e.g., 2- and 3-styrylchromones, xanthones, flavones) and nitrogen (e.g., pyrazoles, triazoles, acridones, 4-quinolones) heterocyclic compounds in order to be assessed as antioxidant, anti-inflammatory, antidiabetic, and anticancer agents has been the main core work of our research interests. Additionally, the synthesis of steroid-type compounds as anti-Alzheimer drugs as well as of several chromophores as important dyes for cellular imagi

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47

S. Silva, Artur M., Ana M. G. Silva, Augusto C. Tomé, and José A. S. Cavaleiro. "New Syntheses of Flavones from Diels–Alder Reactions of 2-Styrylchromones withortho-Benzoquinodimethanes." European Journal of Organic Chemistry 1999, no. 1 (1999): 135–39. http://dx.doi.org/10.1002/(sici)1099-0690(199901)1999:1<135::aid-ejoc135>3.0.co;2-i.

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48

Reddy, B. Parthasarathi, and G. L. David Krupadanam. "The synthesis of 8-allyl-2-styrylchromones by the modified baker-venkataraman transformation." Journal of Heterocyclic Chemistry 33, no. 6 (1996): 1561–65. http://dx.doi.org/10.1002/jhet.5570330602.

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49

Königs, Pia, Olivia Neumann, Olga Kataeva, Gregor Schnakenburg, and Siegfried R. Waldvogel. "Convenient Synthesis of 3-Cinnamoyl-2-styrylchromones: Reinvestigation of the Baker-Venkataraman Rearrangement." European Journal of Organic Chemistry 2010, no. 33 (2010): 6417–22. http://dx.doi.org/10.1002/ejoc.201000957.

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Yang, Chun-Hua, Yang Yang, and Jing-Han Liu. "Platachromone A–D: Cytotoxic 2-styrylchromones from the bark of Platanus×acerifolia (Aiton) Willd." Phytochemistry Letters 6, no. 3 (2013): 387–91. http://dx.doi.org/10.1016/j.phytol.2013.05.003.

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