Araufuranone: A New Phytotoxic Tetrasubstituted Dihydrofuro[3,2-b]furan-2(5H)-One Isolated from Ascochyta araujiae

Araujia hortorum is a perennial vining plant species native to South America. It was introduced into many countries for ornamental and medicinal purposes as well as for its edible fruits, but it has become highly invasive, generating severe environmental problems. Biological control using bioherbicides and natural compounds is an interesting control option. The pathogenic fungus Ascochyta araujiae, isolated from infected leaves of A. hortorum, could be considered as a potential biocontrol agent. Its ability to produce bioactive metabolites was studied. The organic extract of the fungal culture filtrates showed interesting phytotoxic activities consisting of clearly visible necrotic symptoms (0.5–1 cm in diameter) in the punctured leaves. Thus, it was purified; this afforded three main metabolites. These were chemically and biologically characterised: one proved to be a new pentasubstituted dihydrofuro[3,2-b]furan-2(5H)-one, named araufuranone (1). The others were the already known fungal metabolites neovasinin and 2,4-dihydroxy-6-hydoxymethylbenzaldehyde (2 and 3). The structure of araufuranone was determined using spectroscopic methods (essentially 1D and 2D 1H and 13C NMR and HR ESIMS spectra); its relative configuration was assigned by a NOESY spectrum. To the best of our knowledge, araufuranone is the first example of a naturally occurring compound showing that carbon skeleton. Assayed by a puncture, araufuranone proved to be weakly active on the leaves of Diplotaxis sp. and Sonchus sp.; the other two metabolites were even less toxic. Tested on cress, compounds 2 and 3 were able to partially inhibit rootlet elongation whereas araufuranone was almost inactive.


Introduction
Araujia hortorum E. Fourn.(fam.Apocynaceae) (often referred to as Araujia sericifera Brot.) is a perennial fast-growing vining plant species native to South America.It was introduced into many countries (e.g., Europe, South Africa, and New Zealand among others) for ornamental and medicinal purposes as well as for its edible fruits, but it has become highly invasive, generating serious environmental problems mainly in natural habitats [1][2][3][4][5][6][7].
The search for biological control agents led to proposal of the rust fungus Puccinia araujiae Lev. in New Zealand [8][9][10].More recently, Ascohyta araujiae Speg.was identified in Argentina as the causal agent of necrotic leaf spots and defoliation of A. hortorum [11].It was evaluated, together with the fungus Septoria araujiae, as a possible biocontrol agent of the weed, alone or in combined treatments [12].Considering that A. araujiae is a necrotrophic pathogen, and after observing a few of the caused symptoms (i.e., necrotic spots and chlorosis), the possible production and release of bioactive phytotoxic metabolites by the fungus during the infection process was hypothesised.Therefore, the fungus was grown in vitro and its culture filtrates, having promising phytotoxic activities, were extracted and purified.
This manuscript reports the isolation and chemical and biological characterisation of the bioactive metabolites produced by A. araujiae grown in vitro.

General Experimental Procedures
Optical rotations were measured using a Jasco P-1010 digital polarimeter (Tokyo, Japan).The IR spectra were recorded as a glassy film on a Perkin-Elmer (Waltham, MA, USA) Spectrum One Fourier transform infrared (FTIR) spectrometer.The UV spectra were recorded on a JASCO V-530 (Tokyo, Japan) spectrophotometer in a CH 3 CN solution.The 1 H and 13 C NMR spectra were recorded in CD 3 OD at 400 or 500 and 100 or 125 MHz on Bruker (Karlsruhe, Germany) and Varian (Palo Alto, CA, USA) instruments using the same solvent as the internal standard.The carbon multiplicity was determined by a DEPT spectrum [13].The COSY-45, HSQC, HMBC, and NOESY spectra were recorded using Bruker and Varian microprograms [13].The HRESI and ESI mass spectra and liquid chromatography (LC)/MS analyses were performed using the LC/MS TOF Agilent 6230B HPLC 1260 Infinity system (Milan, Italy).The HPLC separations were performed with a Phenomenex LUNA (C18 (2) for 5 µ at 150 × 4.6 mm.Analytical and preparative TLCs were carried out on silica gel (Kieselgel 60, F 254 ; 0.25 and 0.5 mm, respectively) or on reverse phase (Whatman, KC18 F 254 ; 0.20 mm) plates (Merck, Darmstadt, Germany).The spots were visualised by exposure to UV radiation or by spraying first with 10% H 2 SO 4 in MeOH and then with 5% phosphomolybdic acid in EtOH, followed by heating at 110 • C for 10 min.Column chromatography was performed using silica gel (Kieselgel 60, 0.063-0.200mm) (Merck).

Fungal Isolates and Culture Conditions
The strain of Ascochyta araujiae used in this study was isolated from the necrotic leaf spots of Araujia hortorum sampled at San Andrés de Giles, Buenos Aires, Argentina.The fungus pathogen was identified based on previously described morphological characteristics such as the colony growing in potato glucose agar, pycnidia, and conidia [12,14] Afterwards, the internal transcribed spacer (ITS) region and the large subunit (LSU) of the nuclear ribosomal RNA were partially sequenced.The ITS1-5.8S-ITS2 region (ITS) of the nuclear ribosomal DNA operon was amplified and sequenced with the V9G [15] and ITS4 [16] primer pair and the primer combination of LR0R [17] and LR7 [18] was used for the LSU amplification and sequencing.For future reference, the nucleotide sequence data were deposited in the NCBI GenBank database under the accession numbers OP237030 (ITS) and OP237029 (LSU).To our knowledge, these are the first records of gene sequences available for A. araujiae.The strain was stored and grown in the laboratories of the Institute of Sciences of Food Production, CNR, Bari, Italy.For the production of bioactive metabolites, the fungus was preliminarily grown in different growth conditions.Among those tested, the best proved to be a defined mineral medium, M-1-D [19].The fungus from actively growing colonies was transferred into Erlenmeyer flasks (1 L) containing 300 mL of the cited medium and grown in shaken conditions for 20 days at 25 • C in the dark.The mycelium was removed by filtration and the liquid cultures were lyophilised prior to the extraction procedure.

Phytotoxic Assays 2.4.1. Bioassay on Phelipanche ramosa Seeds
For the bioassay on the parasitic weed Phelipanche ramosa (L.) Pomel, a protocol for seed conditioning and germination was used [20].The filters were cut into smaller square pieces, each containing around 100 conditioned seeds, and placed in Petri dishes.A solution (0.5 mL) with the metabolites (0.1 mg metabolite/mL solution) and the synthetic stimulant (GR24) were added over the filters.The Petri dishes were kept in the dark at 25 • C to allow germination.After five days, the number of germinated seeds was determined in comparison with the control.

Bioassay on Punctured Leaves
The leaves of six weed species (namely, Calamintha sp., Cyperus sp., Convolvulus arvensis L., Diplotaxis sp., Heliotropium europeum L., and Sonchus sp.) were harvested from plants growing in naturally infested fields in the countryside of Bari (Southern Italy).Uniform leaves were chosen and then immediately placed in polycarbonate boxes on suitable trays.The leaf surface was injured using an insulin syringe needle, thus provoking small and superficial wounds immediately before the droplet application.Each leaf received 30 µL of the solution containing 0.8 mg metabolite/mL H 2 O. Three replicates were prepared for each treatment and for each plant species.The boxes were kept at ±25 • C under continuous light.The eventual appearance of the symptoms of phytotoxicity was observed up to 5 days.

Bioassay on Garden Cress (Lepidium sativus L.) Seeds
Garden cress (Lepidium sativus L. fam.Brassicaceae) seeds were purchased from Emanuele Larosa Seeds (Andria, Italy).This species was chosen because of its high germinability and uniform seedling growth.Briefly, the metabolites were dissolved in methanol and then diluted in methanol-water (2:98, v/v) to obtain a final concentration of 0.2 mg/L.The L. sativus seeds were sanitised with a 1% sodium hypochlorite solution (v/v) for 10 min and soaked with distilled water.Batches of ten seedlings (one batch for each treatment) were transferred to the filter paper in small Petri dishes (6 cm in diameter).Each filter was moistened with 1 mL of the solution.Each treatment was replicated three times.The plates were placed in a growth chamber at 25 • C with a photoperiod of 12 h light/12 h dark for 3 days.Methanol (2% in water) was added as a control treatment.After 3 days, the germination percentage and the rootlet lengths were measured in comparison with the untreated control.

Results and Discussion
In a first screening comparing the different cultural conditions (shaken vs. still; liquid vs. solid), the shaken liquid culture was identified as the best for the production of bioactive filtrates.The purification process of the phytotoxins was bioguided using the three different bioassays to test the phytotoxicity, as detailed described in the "Section 2".It began with the assay by a leaf puncture of six weed species (namely, Calamintha sp., Cyperus sp., Convolvulus arvensis L., Diplotaxis sp., Heliotropium europeum L., and Sonchus sp.) of the fungal culture filtrates and the organic extract.Both showed an interesting phytotoxicity consisting of clearly visible necrotic symptoms (0.5-1 cm in diameter); the corresponding aqueous phase showed no activity, demonstrating that the extraction process was exhaustive.The organic extract was then purified by column chromatography and all the fractions collected were assayed for phytotoxicity.Among them, only the active fractions were further purified by TLC to obtain the three pure metabolites, whose chemical and phytotoxic activity are described in the present manuscript.Two of them were known fungal metabolites and were identified as neovasinin and 2,4-dihydroxy-6-hydoxymethylbenzaldehyde, as reported below.The third was a new pentasubstituted dihydrofuro[3,2-b]furan-2(5H)-one, and was named araufuranone (1, Figure 1).
Araufuranone (1) had a molecular formula of C 15 H 22 O 5 , as deduced from its HR ESIMS spectrum, and was consistent with five hydrogen deficiencies.The preliminary investigation of its 1 H and 13 C NMR spectra showed the presence of signals typical of carbonyl, olefinic, hydroxylated methine, aliphatic methylene, and vinyl and aliphatic methyl groups [21,22].These structural features agreed with the bands due to the hydroxy, carbonyl, and olefinic groups observed in the IR spectrum [23] and the absorption maxima due to the extended conjugated groups measured in the UV spectrum [21].
In particular, the 1 H and COSY spectra (Table 1 and Figures S1 and S2) [13] showed the presence of a double doublet (J = 9.4 and 1.2 Hz) at δ 5.22 of an olefinic proton (H-4 ) belonging to a trisubstituted double bond, which, coupled with the adjacent methine proton (H-5 ) observed as a multiplet at δ 2.43.Araufuranone (1) had a molecular formula of C15H22O5, as deduced from its HR ESIMS spectrum, and was consistent with five hydrogen deficiencies.The preliminary investigation of its 1 H and 13 C NMR spectra showed the presence of signals typical of carbonyl, olefinic, hydroxylated methine, aliphatic methylene, and vinyl and aliphatic methyl groups [21,22].These structural features agreed with the bands due to the hydroxy, carbonyl, and olefinic groups observed in the IR spectrum [23] and the absorption maxima due to the extended conjugated groups measured in the UV spectrum [21].
In particular, the 1 H and COSY spectra (Table 1 and Figures S1 ans S2) [13] showed the presence of a double doublet (J = 9.4 and 1.2 Hz) at δ 5.22 of an olefinic proton (H-4′) belonging to a trisubstituted double bond, which, coupled with the adjacent methine proton (H-5′) observed as a multiplet at δ 2.43.
The latter proton (H-5′), also coupled with the protons of the adjacent methyl (H3-8′) and methylene (H2-6′) groups, which resonated as a doublet (J = 6.9 Hz) and a multiplet at δ 0.98 and 1.29, respectively.The multiplet of H2-6′ also coupled with the methyl group (H3-7′) appeared as a triplet (J = 7.3 Hz) at δ 0.91, and represents the terminal carbon of the 4-mehtylhexen-2-enyl residue [23].The presence of this side chain was also supported by the long-range couplings observed in the HMBC spectrum (Table 1 and Figure S5) [13] between the two olefinic carbons C-3′ and C-4′, which appeared in the 13 C NMR spectrum(Table 1 and Figure S3) as a singlet and a doublet at δ 130.5 and 138.0, respectively.C-3′ coupled with H3-2′, the first methyl of the side chain, which resonated at δ 12.4,CH3/1.81,brs whereas C-4′, coupled with the same methyl and the other (H3-8′), which was observed at δ 19.7,CH3/0.98,dFurthermore, in the COSY spectrum, an allylic coupling (J = 1.2 Hz) was observed between H-4′ and H3-2′.This 4-mehtylhexen-2-enyl side chain was bonded to the secondary carbon (HC-5), which resonated at δ 80.3,CH/4.37s of a trihydrofuran ring.This was supported by the HMBC coupling observed between C-2′, C-3′, and C-4′ with H-5.The presence of a trisubstituted furan ring was suggested by the typical signal of the two sp 3 quaternary and one sp 2 tertiary carbons as C-6, C-6a, and C-3a, which appeared in the 13 C NMR spectrum at δ 68.1, 94.8, and The latter proton (H-5 ), also coupled with the protons of the adjacent methyl (H 3 -8 ) and methylene (H 2 -6 ) groups, which resonated as a doublet (J = 6.9 Hz) and a multiplet at δ 0.98 and 1.29, respectively.The multiplet of H 2 -6 also coupled with the methyl group (H 3 -7 ) appeared as a triplet (J = 7.3 Hz) at δ 0.91, and represents the terminal carbon of the 4-mehtylhexen-2-enyl residue [23].The presence of this side chain was also supported by the long-range couplings observed in the HMBC spectrum (Table 1 and Figure S5) [13] between the two olefinic carbons C-3 and C-4 , which appeared in the 13 C NMR spectrum (Table 1 and Figure S3) as a singlet and a doublet at δ 130.5 and 138.0, respectively.C-3 coupled with H 3 -2 , the first methyl of the side chain, which resonated at δ 12.4,CH 3 /1.81,brs whereas C-4 , coupled with the same methyl and the other (H 3 -8 ), which was observed at δ 19.7,CH 3 /0.98,dFurthermore, in the COSY spectrum, an allylic coupling (J = 1.2 Hz) was observed between H-4 and H 3 -2 .This 4-mehtylhexen-2-enyl side chain was bonded to the secondary carbon (HC-5), which resonated at δ 80.3,CH/4.37s of a trihydrofuran ring.This was supported by the HMBC coupling observed between C-2 , C-3 , and C-4 with H-5.The presence of a trisubstituted furan ring was suggested by the typical signal of the two sp 3 quaternary and one sp 2 tertiary carbons as C-6, C-6a, and C-3a, which appeared in the 13 C NMR spectrum at δ 68.1, 94.8, and 157.0, respectively.In the HMBC spectrum, C-6 correlated with H-5 and the geminal methyl group H 3 -9 , which resonated at δ 18.5,CH 3 /1.38,s;C-6a coupled with H-5 and C-3a coupled with H 3 -9 .The trihydrofuran ring was side-fused to a furanone ring, being the head-bridge carbons C-3a and C-6a.Consequently, the 13 C NMR spectrum showed two sp 2 carbons at δ 166.5, typical of a carbonyl (C-2) of an α,β-unsaturated γ-lactone ring and the other (C-3) at δ 98.4, typical of a tertiary carbon of a tetrasubstituted double bond, which was oxygenated [22].These findings were confirmed by the couplings observed in the HMBC spectrum between both C-2 and C-3, with H 3 -1 , which is the residual vinyl methyl group bonded to C-3, resonating at δ 7.2,CH 3 /1.90,s.The presence of pentasubstituted dihydrofuro[3,2-b]furan-2(5H)-one in 1 was supported by the couplings observed in the HMBC spectrum between C-3a and C-6 with H 3 -9 [21,22].The investigation of the HSQC (Table 1and Figure S4) [13] spectrum allowed us to assign the chemical shifts to the protonated residual carbons; thus, the chemical shift values were assigned to all the protons and corresponding carbons, as listed in Table 1.Therefore, 1 was formulated as 6,6a-dihydroxy-3,6-dimethyl-5-(4-methylhex-2en-2-yl)-6,6a-dihydrofuro[3,2-b]furan-2(5H)-one.
The structure assigned to araufuranone was supported by the other couplings observed in the HMBC spectrum (Table 1 and Figure 2) as well as from the data of its HR ESIMS spectrum (Figure S7).This latter spectrum showed the sodium adduct ion [M + Na] + at 305.1370 m/z.The structure assigned to araufuranone was supported by the other couplings observed in the HMBC spectrum (Table 1 and Figure 2) as well as from the data of its HR ESIMS spectrum (Figure S7).This latter spectrum showed the sodium adduct ion [M + Na] + at 305.1370 m/z.The relative stereochemistry of 1 was determined by a NOESY spectrum (Figures 3  and S6) [13].As shown in Figure 3, the correlation between H-5 and H3-9′ allowed us to assign a cis-stereochemistry between the OH group at C-6 and the side chain bonded at C-5 of the trihydrofuran ring.This was supported by the correlation observed between H-4′ and H-5.Furthermore, the already cited correlation between H-5 and H3-9′ and the lack of any correlation between H-4′ and H3-2′ allowed us to assign an E-stereochemistry to the double of the side chain.Considering the very low amount of 1, which also withstood crystallisation and was used for the biological assays, it was not possible to assign its absolute configuration.The relative stereochemistry of 1 was determined by a NOESY spectrum (Figures 3  and S6) [13].As shown in Figure 3, the correlation between H-5 and H 3 -9 allowed us to assign a cis-stereochemistry between the OH group at C-6 and the side chain bonded at C-5 of the trihydrofuran ring.The structure assigned to araufuranone was supported by the other couplings observed in the HMBC spectrum (Table 1 and Figure 2) as well as from the data of its HR ESIMS spectrum (Figure S7).This latter spectrum showed the sodium adduct ion [M + Na] + at 305.1370 m/z.The relative stereochemistry of 1 was determined by a NOESY spectrum (Figures 3  and S6) [13].As shown in Figure 3, the correlation between H-5 and H3-9′ allowed us to assign a cis-stereochemistry between the OH group at C-6 and the side chain bonded at C-5 of the trihydrofuran ring.This was supported by the correlation observed between H-4′ and H-5.Furthermore, the already cited correlation between H-5 and H3-9′ and the lack of any correlation between H-4′ and H3-2′ allowed us to assign an E-stereochemistry to the double of the side chain.Considering the very low amount of 1, which also withstood crystallisation and was used for the biological assays, it was not possible to assign its absolute configuration.This was supported by the correlation observed between H-4 and H-5.Furthermore, the already cited correlation between H-5 and H 3 -9 and the lack of any correlation between H-4 and H 3 -2 allowed us to assign an E-stereochemistry to the double of the side chain.Considering the very low amount of 1, which also withstood crystallisation and was used for the biological assays, it was not possible to assign its absolute configuration.
Fungal furans and furanones containing bioactive metabolites are well-known [24][25][26][27]; however, there are no natural products containing dihydrofuro [3,2-b]furan-2(5H)-one.Currently, there is only one deposited patent reporting the synthesis of dihydrofuranfuranone derivatives as antitumor agents [28].Thus, araufuranone is the first fungal metabolite belonging to this group of natural compounds to be isolated for the first time from A. araujiae.The metabolites most similar to 1 are neovasinin and penpolonin analogues [29][30][31] The two already known metabolites were identified as neovasinin and 2,4-dihydroxy-6-hydroxymethylbenzaldehyde (2 and 3, respectively; Figure 1) by a comparison of their physical and spectroscopic data with those reported in the literature by Nakajima et al. [29] and Ballantine et al. [32] for 2 and 3, respectively.The attribution of the chemical shift of all the protons and corresponding carbon of 2 were supported by the couplings observed in its COSY, HSQC, and HMBC spectra [13].In particular, its NOESY spectrum showed the correlation between Me-16 and H-10, which allowed us to confirm the E-configuration of the double bond of the side chain linked to C-7.Furthermore, the correlation observed between H-7 and Me-15, considering that the dihydropyran ring assumed a pseudochair conformation, allowed us to also confirm their axial-equatorial location or vice versa Neovasinin (2) was first isolated from Neocosmospora vasinfecta E. F. Smith, which is a fungal pathogen causing root-and fruit-rot as well as seedling damping-off in many crops (e.g., pepper, peanuts, and soybeans) [30].From the same fungus was also isolated a previously undescribed α-pyrone, named neovasinone [31].When assayed on lettuce (Lactuca sativa) seedlings, neovasinin weakly inhibited the root elongation [29] whereas neovasinone caused the stimulation of root seedlings [31].These results demonstrate that the carbonyl group of the right α-pyrone ring present in neovasinone plays an important role in imparting activity [29].The partial stereochemistry of neovasinin, which has been characterised by spectroscopic and chemical methods, was also reported from the same authors and a few of them also assigned its absolute configuration by a combination of an X-ray analysis and a degradation reaction [33].Neovasinin was successively isolated, together with a plethora of other metabolites, from Penicillium sp.SYPF7381, which was obtained from the rhizosphere soil of Pulsatilla chinensis (Bunge) Regel collected from Huludao in the Liaoning province of China.Neovasinin showed a significant inhibition of NO production [34].Similarly, 2 was also isolated, together with other metabolites from the co-culture of Aspergillus fumigatus D Fresenius and Fusarium oxysporum R1 Snyder & Hansen, collected from two traditional medicinal plants, Edgeworthia chrysantha Lindl.and Rumex madaio Makino.The metabolites did not show toxicity against human pathogens [35].Finally, 2 was isolated, together with five undescribed α-pyrones named penpolonins A-E, from the endophytic fungus Penicillium polonicum Zalessky collected from the roots of Camptotheca acuminata Decne, showing a moderate cytotoxic activity [36].Neovasinin showed phytotoxic activity [29].Penpolonins were only assayed for cytotoxicity in comparison with neovasinin; their phytotoxic activity was not tested.Neovasinin and two penpolonins showed cytotoxic activity against the Hep-2 and TU212 human laryngeal cancer cell lines [36].
2,4-Dihydroxy-6-hydroxymethylbenzaldehyde (3) was previously isolated, together with a few other aromatic analogues, from the culture filtrates of Aspergillus rugulosus I.M.I. 84338 [21] and successively together with several other metabolites from Clematis mandshurica Rupr., which is a traditional crude drug for the treatment of urethritis, carbuncles, and carcinomas [37].
In the puncture assay at the tested concentrations (see above), araufuranone proved to be weakly active on the leaves of only two plant species, Diplotaxis sp. and Sonchus sp., whereas the other two metabolites were even less toxic and only on Diplotaxis (data not shown).On cress, compounds 2 and 3 were able to partially inhibit rootlet elongation (around 20%; data not shown) whereas araufuranone was almost inactive.None of the metabolites caused a reduction in the germination capability of the seeds.On P. ramosa seeds, the compounds were completely inactive at the tested concentrations.Although the phytotoxic activity of the three metabolites seemed to be plant species-dependent, the high activity of the fungal culture filtrates and corresponding organic extract (that could be due to additives or the synergistic activity of the three metabolites) suggested a further in-depth investigation is required on its activity aimed at its potential application as bioherbicides.Further studies should be also carried out on the phytotoxic and other potential biological activities of the pure metabolites.Furthermore, the cytotoxic activity of neovasinin also suggests its potential application in medicine, as well as to test the related aurofuranone to investigate this type of activity.

Conclusions
A new phytotoxic tetrasubstituted dihydrofuro [3,2-b]furan-2(5H)-one was isolated together with neovasinin and a trisubstituted benzaldehyde from A. araujiae, proposed as a potential mycoherbicide for the biocontrol of the noxious weed A. hortorum.Aurofuranone is, to the best of our knowledge, the first example of a naturally occurring compound showing the described carbon skeleton.It showed to be weakly active on the leaves of two weed species, Diplotaxis sp. and Sonchus sp.; the other two metabolites were even less toxic.However, the weak toxicity of the pure metabolites compared with the stronger biological activity of the fungal culture filtrates and the corresponding organic extract

Figure 2 .
Figure 2. The most significant COSY and HMBC correlations observed in the corresponding spectra of 1.

Figure 3 .
Figure 3. Significant NOE correlations observed in the NOESY spectrum of 1.

Figure 2 .
Figure 2. The most significant COSY and HMBC correlations observed in the corresponding spectra of 1.

Figure 2 .
Figure 2. The most significant COSY and HMBC correlations observed in the corresponding spectra of 1.

Figure 3 .
Figure 3. Significant NOE correlations observed in the NOESY spectrum of 1.

Figure 3 .
Figure 3. Significant NOE correlations observed in the NOESY spectrum of 1.
, and thus the relative configuration of R* and S* to C-6 and C-7, respectively.The ESIMS spectrum of neovasinin, recorded in a positive modality, showed the potassium [M + K] + , sodiated [M + Na] + , and protonated [M + H] + adduct ions at m/z 347, 331, and 309, respectively.The same spectrum recorded in a negative modality showed the pseudomolecular ion [M − H] − at m/z 307.The ESIMS spectrum of the trisubstituted benzaldehyde (3) showed the sodiated adduct ion [M + Na] + at 191 m/z.