Synthesis, fluorescence properties and the promising cytotoxicity of pyrene–derived aminophosphonates

  1. Jarosław Lewkowski1,
  2. Maria Rodriguez Moya1,
  3. Anna Wrona-Piotrowicz1,
  4. Janusz Zakrzewski1,
  5. Renata Kontek2 and
  6. Gabriela Gajek2

1Department of Organic Chemistry, Faculty of Chemistry, University of Łódź, Tamka 12, 91-403 Łódź, Poland
2Laboratory of Cytogenetics, Faculty of Biology and Environmental Protection, University of Łódź, Banacha 12/16, 90-237 Łódź, Poland

  1. Corresponding author email

Associate Editor: C. Stephenson
Beilstein J. Org. Chem. 2016, 12, 1229–1235. doi:10.3762/bjoc.12.117
Received 08 Mar 2016, Accepted 01 Jun 2016, Published 16 Jun 2016


A large series of variously substituted amino(pyren-1-yl)methylphosphonic acid derivatives was synthesized using a modified aza-Pudovik reaction in 20–97% yields. The fluorescence properties of the obtained compounds were investigated revealing that N-alkylamino(pyren-1-yl)methylphosphonic derivatives are stronger emissive compounds than the corresponding N-aryl derivatives. N-Benzylamino(pyren-1-yl)methylphosphonic acid displayed strong fluorescence (ΦF = 0.68) in phosphate-buffered saline (PBS). The influence of a series of derivatives on two colon cancer cell lines HT29 and HCT116 was also investigated. The most promising results were obtained for N-(4-methoxyphenyl)amino(pyren-1-yl)methylphosphonate, which was found to be cytotoxic for the HCT116 cancer cell line (IC50 = 20.8 μM), simultaneously showing weak toxicity towards normal lymphocytes (IC50 = 230.8 µM).

Keywords: aminophosphonic derivatives; cytotoxicity; fluorescence properties; MTT test; pyrene-1-carboxaldehyde


The biological activity of aminophosphonic systems is very well known and described, in aspect of their crop protective [1], antibacterial [2] or anticancer properties [3]. Various C-aryl substituted derivatives of phosphonoglycine have been synthesized including those of benzene and several polycyclic aromatic hydrocarbons [4], five- [5] and six-membered [6] heteroaromatic compounds and even ferrocene [7]. In contrast, pyrene-based derivatives, e.g., amino(pyrene-1-yl)methyl phosphonic acid derivatives have been described only twice in the chemical literature. Firstly, Harry Hudson’s team [8] published the synthesis of diethyl N-benzhydrylamino(pyrene-1-yl)methylphosphonate in a series of N-benzhydryl substituted aminomethyl phosphonates. Recently, an Indian group [9] reported the synthesis of a number of N-aryl substituted, diethyl amino(pyrene-1-yl)methyl phosphonates and some preliminary studies on their fluorescence properties.

Such a poor knowledge about these compounds is astonishing in the light of the fact that the phosphonic analogues of phenylglycine, exhibited their herbicidal activity [10], and are used as plant growth regulators [10], agrochemical fungicides [11,12] and glutamate receptor modulators [13]. It is therefore expectable that C-pyrene derivatives may have similar or even more promising biological properties.

This expectation is supported by the biological activity of azomethine derivatives of pyrene-1-carboxaldehyde. They show antimicrobial action, e.g., 1-phenytoinylacetic acid hydrazone of pyrene-1-carboxaldehyde demonstrated a moderate antimicrobial activity towards Escherichia coli and Staphylococcus aureus [14]. Azomethine derivatives of pyrene-1-carboxaldehyde have shown enzyme inhibitory activity, as, e.g., its thiosemicarbazone, which is able to inhibit the action of urease [15].

Although fluorescence properties of pyrene-based aminophosphonic derivatives have been mentioned only once in a preliminary form [9], fluorescence emission of their azomethine precursors was reported for pyrene-1-carboxaldehyde thiosemicarbazone and Schiff bases as well as their metal complexes [16-21]. Such properties were described for, e.g., ruthenium(II) complexes of (5-chloropyridin-2-yl)-(pyren-1-yl)methyleneamine [17], a N-(1-pyrene)methylideneglucosamine mercury complex [18], a N-(pyren-1-ylidene)-2-hydroxyaniline-copper(II) and -zinc(II) complexes [19] or N-(pyren-1-ylidene)-4-carboxyaniline-Fe(II) and -Cr(III) complexes [20]. Several phosphorus-supported ligands containing a pyrene-1-carbimino moiety [21] were found to be fluorescence-based sensors of Cu(II) and Mg(II) cations.

Considering all above, we decided to synthesize a series of N-substituted derivatives of C-(pyren-1-yl)phosphonoglycine and to investigate their cytotoxic and fluorescence properties.

Results and Discussion

Synthesis of aminophosphonic acid derivatives 3, 4 and 5

Schiff bases 1ah were prepared by refluxing pyrene-1-carboxaldehyde with an amine in methanol, hexane or dichloromethane for 24 hours and were used for further conversions as obtained. This harsh method to prepare imines had to be used, because the simple mixing of reagents in methanol at room temperature, which is the common mode d’emploi in such cases [5,7], did not provide satisfactory results. The reaction completion was monitored by 1H NMR and obtained imines 1ah were isolated by simple evaporation of the solvent and were used for the further reaction without purification.

Aminophosphonates 3Aah, 3Bae and 3Cad, 3Cg have been synthesized via an aza-Pudovik reaction [22], i.e., the addition of the appropriate phosphite 2AC to the azomethine bond of the Schiff bases 1ah. Nevertheless, the important modifications had to be introduced to the described procedures [22,23]. The 1-pyrene moiety is a troublesome substituent due to its spatial volume, which tends to disturb in the course of the reactions. Attempts to use any of common solvents failed as no or only a weak progress of the reaction was noticed (Scheme 1). The best solution was to apply phosphites simultaneously as solvents and reactants, which however forced to use them in a high excess. This necessity resulted in troubles with purification, implicating a particular approach to each case.


Scheme 1: Synthesis of aminophosphonates 3Aaj, 3Bae, 3Cad, 3Cg, aminophosphonic acids 4a, 4c and hydroxyphosphonate 5A.

Dimethyl aminophosphonates 3AaAh were purified by washing their dichloromethane solutions with a saturated aqueous sodium bicarbonate solution, which allowed to remove dimethyl phosphite. This procedure was followed by column chromatography, and, in a case of N-benzyl derivative 3Aa, triturating the product with diethyl ether until the precipitation of a solid was additionally carried out.

The isolation and purification of diethyl aminophosphonates 3Bae required a different method. To isolate them, the crude reaction mixtures were dissolved in a minimum amount of diethyl ether and triturated until a yellow precipitate formed. This operation was repeated twice. Aminophosphonates 3Bae were purified by column chromatography.

The most complex procedure was used to isolate and to purify the dibenzyl aminophosphonates 3Cad and 3Cg. The crude reaction mixtures were dissolved in small amounts of pyridine and then, treated with elemental iodine to decompose dibenzyl phosphite. This was followed by washing the mixture dissolved in dichloromethane with saturated aqueous solutions of sodium thiosulfate and then sodium bicarbonate. The purification with column chromatography allowed to afford pure products in satisfactory yields.

Due to the fact that we were not able find proper conditions to prepare N-(pyren-1-ylidene)-tert-butylamine (1j) and dimethyl N-(tert-butyl)amino(pyren-1-yl)methylphosphonate (3Aj) via the aza-Pudovik reaction, the Kabachnik–Fields reaction was used as an alternative method [23]. The three-component reaction without any catalyst was carried out first in dichloromethane then, in methanol. In both cases, to our surprise, no traces of the desired aminophosphonate 3Aj have been found in the reaction mixture. Instead, dimethyl hydroxy(pyren-1-yl)methylphosphonate (5A) was obtained in quite satisfactory yield. Dimethyl N-(tert-butyl)amino(pyren-1-yl)methylphosphonate (3Ai) was obtained, when the Kabachnik–Fields reaction was carried out in the presence of a catalytic amount of trifluoroacetic acid in refluxing acetonitrile. The same procedure, i.e., the Kabachnik–Fields reaction in the presence of trifluoroacetic acid, but in refluxing methanol has been successfully used for the preparation of dimethyl N-(m-methylphenyl)amino(pyren-1-yl)methylphosphonate (3Ai) (Scheme 1).

Interestingly, attempts to obtain the hydroxyphosphonate 5A in conditions typical for the Pudovik (not aza) reaction failed – the product could be obtained only when tert-butylamine (or isopropylamine) was present in the reaction mixture (Scheme 1).

All obtained aminophosphonates 3Aaj, 3Bae, 3Cad and 3Cg as well as the hydroxyphosphonate 5A gave satisfactory results of in the elemental analysis and were characterized by means of 1H, 13C and 31P NMR and IR spectroscopy with all signals attributed to each nucleus. Compounds were also characterized by melting point measurements.

Jayaprakash et al. [9] reported the synthesis of several pyrene-derived aminophosphonates via a silica-catalyzed Kabachnik–Fields reaction. Among others, they synthesized three amino-phosphonates 3Bbd, reporting their melting point values and their spectral characterizations. Melting point values quoted by the authors differed from values measured by us. The reason of such a discrepancy remains unclear, it might be caused by the different eluents used – we eluted products using chloroform, while Jayaprakash et al. [9] used hexane and ethyl acetate (2:3).

The other discrepancy concerns the 1H NMR spectra, and particularly their aromatic regions. In all three cases, Jayaprakash et al. [9] quoted all aromatic signals as broad multiplets, whereas we were capable to distinguish clearly signals of pyrene protons as a series of distinct doublets and approximate triplets. Phenyl ring signals were also visible, e.g., the non-substituted phenyl ring gave a triplet, doublet of doublets and a doublet, the 4-methyl substituted phenyl moiety demonstrated a distinct AA’XX’ system, whereas the 4-methoxy derivative shows an AA’BB’ system. All these phenomena are clearly visible in the 1H NMR spectra and scans of them are collected in Supporting Information File 1.

Aminophosphonic acids 4a and 4c were prepared using the classical cleavage of dimethyl aminophosphonates 2Aa and 2Ac with trimethylsilyl bromide in dry dichloromethane. After 24-hours reaction, the reaction was quenched by methanol to give, after routine work-up the desired acids 4a and 4c (Scheme 1). They were characterized by NMR spectroscopy (1H, 13C and 31P), IR spectroscopy, melting point measurements and elemental analysis.

The obtained phosphonic derivatives were then selected and their biological and photophysical properties were studied.

Luminescent properties of pyrenyl aminophosphonates

The widespread use of pyrene derivatives as luminescent probes in biological research [24-27] prompted us to study emissive properties of the synthesized aminophosphonates. We have measured their electronic absorption and emission spectra in chloroform solution. Although photodecomposition of pyrene in this solvent has been reported [28], we found that this is not the case of the compounds under study. To avoid excimer formation, spectra were recorded at low sample concentrations (1 μM). We have found that all compounds under study were emissive albeit emission quantum yields varied from ≈0.01 to ≈0.7 (Table 1). The typical absorption and emission spectrum (those of compound 3Aj), compared with the spectra of pyrene are shown in Figure 1. The spectra are closely similar and show vibronic structure characteristic for monomeric fluorophores. The spectra of 5 are slightly shifted bathochromically (9 nm and 4 nm for the absorption and emission spectrum, respectively) in comparison to the spectra of pyrene. In this context, it should be noticed that spectra reported in [9] were measured at significantly higher concentrations (0.5 mM) and are broad and structureless. Therefore, they should rather be assigned to fluorophore aggregates (excimers).

Table 1: Absorption and emission maxima and fluorescence quantum yields (ΦF) for the synthesized compounds in chloroform solution (c = 1 μM).

Compd. Absorption
λmax (nm)
λmax (nm)
3Aa 304, 317, 330, 347 378, 388, 399 0.06
3Ba 304, 316, 331, 347 378, 388, 398 0.06
3Ca 304, 316, 331, 348 378, 389, 399 0.06
3Ab 304, 317, 331, 348 382, 397, 424, 444 <0.01
3Bb 304, 318, 330, 348 382, 397, 443 <0.01
3Cb 305, 318, 332, 349 382, 397, 455 <0.01
3Ac 304, 317, 331, 348 380, 395, 485 <0.01
3Bc 304, 316, 330, 448 380, 395, 484 <0.01
3Cc 304, 317, 330, 448 380, 396, 485 <0.01
3Ad 304, 317, 331, 348 380, 398, <0.01
3Bd 304, 317, 330, 348 380, 398 <0.01
3Cd 304, 317, 331, 348 381, 398 <0.01
3Ae 303, 316, 330, 347 378, 390, 398 0.10
3Be 303, 316, 330, 346 377, 389, 397 0.10
3Af 303, 317, 330, 347 378, 390, 398 0.09
3Ag 316, 330, 347 378, 390, 398 0.05
3Ai 303, 316, 330, 347 380, 395 <0.01
3Aj 318, 331, 347 378, 389, 397 0.11
4ac 303, 316, 329, 345 378, 397, 419 0.68
5A 317, 330, 347 377, 388, 396 0.13

aExcitation was set at the maximum of the lowest energy absorption band. bMeasured for aerated solutions. Quenching by dissolved dioxygen was not observed. cMeasured for an aqueous 0.01 PBS (phosphate-buffered saline) solution (pH 7.4)


Figure 1: Normalized electronic absorption and emission spectra of 3Aj and pyrene in chloroform (c = 1 μM).

The spectra of 3Aj were run in solvents of varied polarity (Figure 2) and display the well-known Ham effect (dependence of the ratio of intensities of III/I vibronic bands on the medium polarity) [26].


Figure 2: Emission spectra of compound 3Aj in various solvents. The spectra are normalized at ≈378 nm (pyrene band I).

The highest emission quantum yield (0.68) was found for aminophosphonic acid 4a in aqueous buffer (pH 7.4). A similar phenomenon of higher emission efficiency of 1-(pyrene-1-carboxamido)methylphosphonic acid in comparison to a corresponding aminophosphonate was earlier reported [29].

The aforementioned data suggest possible application of compound 3Aj (and other exhibiting similar emission quantum yield) as molecular probes monitoring micropolarity of the fluorophore environment. On the other hand, water-soluble 4a might be used for biological imaging.

Investigation of cytotoxic effects of studied compounds

The cytotoxic effects of dimethyl aminophosphonates 3Aa, 3Ab, 3Ac, 3Ad, 3Ai and dimethyl [hydroxy(pyren-1-yl)methyl]phosphonate (5A) were investigated with two human colorectal carcinoma cell lines: HT29 and HCT116 and also on the normal human lymphocytes. For this a standard MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) test was used and results presented as IC50 values (i.e., the concentration of the compound that inhibits 50% growth). The activity of the tested compounds was studied in the concentration range from 5 to 600 µM. The obtained IC50 values are summarized in Table 2.

Table 2: IC50 values on studied compounds.

Compound R1 lymphocytes HT29 HCT116
3Aa CH2Ph IC50 = 89.2 ± 2.9 µM IC50 = 29.2 ± 3.84 µM IC50 = 29 ± 2.37 µM
3Ab Ph IC50 = 334.2 ± 2.59 µM IC50 = 105.8 ± 3.37 µM IC50 = 70.8 ± 2.99 µM
3Ac 4-C6H4-CH3 IC50 = 17.5 ± 4.15 µM IC50 = 15.8 ± 3.44 µM IC50 = 15.9 ± 4.85 µM
3Ad 4-C6H4-OCH3 IC50 = 230.8 ± 3.43 µM IC50 = 24.2 ± 5.12 µM IC50 = 20.8 ± 3.48 µM
3Ai 3-C6H4-CH3 IC50 = 75.8 ± 4.02 µM IC50 = 57.5 ± 5.19 µM IC50 = 20.21 ± 5.63 µM
5A IC50 = 135.8 ± 1.73 µM IC50 = 25.8 ± 4.99 µM IC50 = 40.4 ± 4.53 µM

The activity of tested compounds varied from IC50 = 15.8 µM to 105.8 µM. As it can be seen, the most interesting results were obtained for compound 3Ad, bearing the p-methoxyphenyl moiety (Figure 3). It has exhibited significant cytotoxicity against both tested cancer cell lines HT29 (IC50 = 24.2 µM) as well as HCT116 (IC50 = 20.8 µM) cells, and it simultaneously was not strongly toxic for normal human lymphocytes (IC50 = 230.8 µM). However, HT29 cells were more resistant to 3Ad than HCT116 cells. Therefore, the aminophosphonate 3Ad showed a carcinoma-specific cytotoxicity against human colon cancer cells. A similar correlation was observed for the aminophosphonic derivative 3Ac, which was strongly cytotoxic against both colon cancer cell lines, but in contrast to 3Ad, was also toxic for lymphocytes. Paradoxally, compound 3Ac, bearing a 4-C6H4-CH3 moiety, exhibited the most potent cytotoxicity from all tested compounds: IC50 (HT29) = 15.8 µM and IC50 (HCT116) = 15.9 µM. On the other hand, 3Ac had the highest IC50 value against normal cells from all tested compounds. The compound 3Ab was the less toxic for normal cells (IC50 = 334.2 µM) from among all tested compounds. However, 3Ab was also the least toxic against both tested cancer cell lines HT29 (IC50 = 105.8 µM) and HCT116 (IC50 = 70.8 µM). Compound 5A has exhibited a significant cytotoxicity against HT29 (IC50 = 25.8 µM). For compounds 3Aa and 3Ai, the received results were comparable, except for the results against HT29, the level of the cytotoxicity was slightly higher for 3Ai. Simultaneously, cytotoxicities of both aminophosphonates (3Aa and 3Ai) against normal lymphocytes were rather high (IC50 = 89.2 and 75.8 µM, respectively).


Figure 3: IC50 values of studied compounds.

On the basis of the results presented in Table 1, it can be concluded that the type of functional group has a large influence on the biological properties of the tested compounds. These results indicate that the presence of a methylphenyl group causes a compound to be toxic for normal lymphocytes (3Ac and 3Ai); a similar phenomenon was observed for N-benzyl substitution (3Aa). Results obtained for the α-hydroxyphosphonate 5A (IC50 = 25.8 µM against HT29) give the impact to look for potential anticancer agents among the α-hydroxyphosphonic derivatives.


A large series of various amino(pyren-1-yl)methylphosphonates was prepared using the aza-Pudovik reaction (3Aah, 3Bae, 3Cad, 3Cg) or in the course of the Kabachnik-Fields reaction (3Ai and j). Amino(pyren-1-yl)methylphosphonic acids 4a and 4c were prepared using Boduszek’s methodology [6] and dimethyl hydroxy(pyren-1-yl)methylphosphonate (the Pudovik reaction). The fluorescence properties of the obtained compounds were investigated and N-benzylamino(pyren-1-yl)methylphosphonic acid showed a quantum yield of 68%, while dimethyl tert-butylamino(pyren-1-yl)methylphosphonate (3Aj) gave 11% quantum yield.

The influence of a series of derivatives on two colon cancer cell lines HT29 and HCT116 was also investigated. The most interesting results were obtained for dimethyl N-(4-methoxyphenyl)amino(pyren-1-yl)methylphosphonate 4d, which was found to be cytotoxic for these two colon cancer cell lines (IC50 ≈ 20 μM), but showed nearly no toxicity towards lymphocytes (IC50 ≈ 230 μM). Although, dimethyl N-(4-methylphenyl)amino(pyren-1-yl)methylphosphonate 4c demonstrated important cytotoxicity (IC50 ≈ 15 μM) for both cancer cell lines, it was unfortunately found to be toxic towards normal lymphocytes (IC50 ≈ 17 μM).

More profound studies on biological properties of selected compounds (necrosis vs apoptosis, mechanism of action) are being developed and will be published in the near future.

Supporting Information

Supporting Information File 1: Experimental procedures, characterization of novel compounds, and details of the biological and photophysical study. Scans of 1H, 13C and 31P NMR spectra of all new synthesized compounds.
Format: PDF Size: 1.9 MB Download


Studies were founded by the National Centre of Science of Polish State (NCN), grant no. 2014/13/B/NZ9/02418.


  1. Kafarski, P.; Lejczak, B.; Tyka, R.; Koba, L.; Pliszczak, E.; Wieczorek, P. J. Plant Growth Regul. 1995, 14, 199–203.
    Return to citation in text: [1]
  2. Kafarski, P.; Lejczak, B. Phosphorus, Sulfur Silicon Relat. Elem. 1991, 63, 193–215. doi:10.1080/10426509108029443
    Return to citation in text: [1]
  3. Kafarski, P.; Lejczak, B. Curr. Med. Chem.: Anti-Cancer Agents 2001, 1, 301–312. doi:10.2174/1568011013354543
    Return to citation in text: [1]
  4. Mohd-Pahmi, S. H.; Hussein, W. M.; Schenk, G.; McGeary, R. P. Bioorg. Med. Chem. Lett. 2011, 21, 3092–3094. doi:10.1016/j.bmcl.2011.03.024
    Return to citation in text: [1]
  5. Klimczak, A. A.; Kuropatwa, A.; Lewkowski, J.; Szemraj, J. Med. Chem. Res. 2013, 22, 852–860. doi:10.1007/s00044-012-0065-3
    Return to citation in text: [1] [2]
  6. Boduszek, B. Tetrahedron 1996, 52, 12483–12494. doi:10.1016/0040-4020(96)00727-2
    Return to citation in text: [1] [2]
  7. Lewkowski, J.; Rzeźniczak, M.; Skowroński, R.; Zakrzewski, J. J. Organomet. Chem. 2001, 631, 105–109. doi:10.1016/S0022-328X(01)01011-7
    Return to citation in text: [1] [2]
  8. Hudson, H. R.; Lee, R. J.; Matthews, R. W. Phosphorus, Sulfur Silicon Relat. Elem. 2004, 179, 1691–1709. doi:10.1080/10426500490466274
    Return to citation in text: [1]
  9. Jayaprakash, S. H.; Rao, K. U. M.; Krishna, B. S.; Prasad, S. S.; Sundar, C. S.; Reddy, C. S. Phosphorus, Sulfur Silicon Relat. Elem. 2015, 190, 449–460. doi:10.1080/10426507.2014.948621
    Return to citation in text: [1] [2] [3] [4] [5] [6]
  10. Hudson, H. R. Aminophosphonic and Aminophosphinic Acids and their Derivatives as Agrochemicals. In Aminophosphonic and Aminophosphinic Acids: Chemistry and Biological Activity; Kukhar, V. P.; Hudson, H. R., Eds.; John Wiley and Sons: Chichester, 2000; pp 443–482.
    Return to citation in text: [1] [2]
  11. Maier, L.; Diel, P. J. Phosphorus, Sulfur Silicon Relat. Elem. 1991, 57, 57–64. doi:10.1080/10426509108038831
    Return to citation in text: [1]
  12. Hudson, H. R. Phosphorus, Sulfur Silicon Relat. Elem. 1999, 144, 441–444. doi:10.1080/10426509908546276
    Return to citation in text: [1]
  13. Jane, D. Aminophosphonic and Aminophosphinic Acids and their Derivatives as Agrochemicals. In Aminophosphonic and Aminophosphinic Acids: Chemistry and Biological Activity; Kukhar, V. P.; Hudson, H. R., Eds.; John Wiley and Sons: Chichester, 2000; pp 483–536.
    Return to citation in text: [1]
  14. Ali, O. M.; Amer, H. H.; Mosaad, A. A.; Abdel-Rahman, A. A.-H. Chem. Heterocycl. Compd. 2012, 48, 1043–1049. doi:10.1007/s10593-012-1097-9
    Return to citation in text: [1]
  15. Saeed, A.; Imran, A.; Channar, P. A.; Shahid, M.; Mahmood, W.; Iqbal, J. Chem. Biol. Drug Des. 2015, 85, 225–230. doi:10.1111/cbdd.12379
    Return to citation in text: [1]
  16. Wang, X. M.; Yan, H.; Feng, X. L.; Chen, Y. Chin. Chem. Lett. 2010, 21, 1124–1128. doi:10.1016/j.cclet.2010.04.029
    Return to citation in text: [1]
  17. Mandal, S.; Kundi, V.; Seth, D. K.; Srikanth, K.; Gupta, P. Polyhedron 2014, 80, 290–297. doi:10.1016/j.poly.2014.06.005
    Return to citation in text: [1] [2]
  18. Areti, S.; Hinge, V. K.; Rao, C. P. Carbohydr. Res. 2014, 399, 64–69. doi:10.1016/j.carres.2014.06.014
    Return to citation in text: [1] [2]
  19. Pinheiro, D.; de Castro, C. S.; Seixas de Melo, J. S.; Oliveira, E.; Nuñez, C.; Fernández-Lodeiro, A.; Capelo, J. L.; Lodeiro, C. Dyes Pigm. 2014, 110, 152–158. doi:10.1016/j.dyepig.2014.04.012
    Return to citation in text: [1] [2]
  20. Obali, A. Y.; Ucan, H. I. J. Fluoresc. 2012, 22, 1357–1370. doi:10.1007/s10895-012-1075-8
    Return to citation in text: [1] [2]
  21. Chandrasekhar, V.; Pandey, M. D.; Bag, P.; Pandey, S. Tetrahedron 2009, 65, 4540–4546. doi:10.1016/j.tet.2009.03.098
    Return to citation in text: [1] [2]
  22. Tyka, R. Tetrahedron Lett. 1970, 11, 677–680. doi:10.1016/S0040-4039(01)97800-1
    Return to citation in text: [1] [2]
  23. Zefirov, N. S.; Matveeva, E. D. ARKIVOC 2008, No. i, 1–17. doi:10.3998/ark.5550190.0009.101
    Return to citation in text: [1] [2]
  24. Gonçalves, M. S. T. Chem. Rev. 2009, 109, 190–212. doi:10.1021/cr0783840
    Return to citation in text: [1]
  25. Sinkeldam, R. W.; Greco, N. J.; Tor, Y. Chem. Rev. 2010, 110, 2579–2619. doi:10.1021/cr900301e
    Return to citation in text: [1]
  26. Bains, G.; Patel, A. B.; Narayanaswami, V. Molecules 2011, 16, 7909–7935. doi:10.3390/molecules16097909
    Return to citation in text: [1] [2]
  27. Drummen, G. P. C. Molecules 2012, 17, 14067–14090. doi:10.3390/molecules171214067
    Return to citation in text: [1]
  28. Aguilera-Sigalat, J.; Sanchez-SanMartín, J.; Agudelo-Morales, C. E.; Zaballos, E.; Galian, R. E.; Pérez-Prieto, J. ChemPhysChem 2012, 13, 835–844. doi:10.1002/cphc.201100843
    Return to citation in text: [1]
  29. Wrona-Piotrowicz, A.; Zakrzewski, J.; Gajda, A.; Gajda, T.; Makal, A.; Brosseau, A.; Métivier, R. Beilstein J. Org. Chem. 2015, 11, 2451–2458. doi:10.3762/bjoc.11.266
    Return to citation in text: [1]

© 2016 Lewkowski et al.; licensee Beilstein-Institut.
This is an Open Access article under the terms of the Creative Commons Attribution License (, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (

Back to Article List