(Z)-5-(3′,4′-Bis(benzyloxy)benzylidene)furan-2(5H)-one

: Over the years secondary metabolites have been considered as lead molecules both in their natural form and as templates for medicinal chemistry. Some secondary metabolites such as polyphenols and ﬂavan-3-ols exert beneﬁcial effects after a modiﬁcation by the microbiota. Synthetic precursors of some of these modiﬁed compounds, in turn, carried a γ -alkylidenebutenolide moiety which characterizes a large class of bioactive natural products endowed with a wide range of biological activities. For these reasons stereoselective preparation of γ -alkylidenebutenolide continues to be an important issue for organic chemists. Our objective is to synthetize the novel compound ( Z )-5-(3 (cid:48) ,4 (cid:48) -bis(benzyloxy)benzylidene)furan-2(5 H )-one in a stereocontrolled-one-pot reaction. The product was obtained in good yield. Furthermore, the theoretical investigation of the transition states suggests a new procedure to achieve Z-isomer of β -unsubstituted γ -alkylidenebutenolide. Abstract: Over the years secondary metabolites have been considered as lead molecules both in their natural form and as templates for medicinal chemistry. Some secondary metabolites such as polyphenols and flavan-3-ols exert beneficial effects after a modification by the microbiota. Synthetic precursors of some of these modified compounds, in turn, carried a γ -alkylidenebutenolide moiety which characterizes a large class of bioactive natural products endowed with a wide range of biological activities. For these reasons stereoselective preparation of γ -alkylidenebutenolide continues to be an important issue for organic chemists. Our objective is to synthetize the novel compound ( Z )-5-(3 ′ ,4 ′ -bis(benzyloxy)benzylidene)furan-2(5H)-one in a stereocontrolled-one-pot reaction. The product was obtained in good yield. Furthermore, the theoretical investigation of the transition states suggests a new procedure to achieve Z-isomer of β -unsubstituted γ -alkylidenebutenolide.


Introduction
Plant-derived compounds have successfully inspired the drug discovery process which has exploited the entire structure of such natural products or part of that to develop new medicinal drugs [1,2].
Polyphenols and related compounds are secondary metabolites which occur naturally in plants and which have been reported to display protective effects in plant-based diet [3].
Indeed, food containing polyphenols are known to exert beneficial effects after long term consumption offering protection against the development of cancers, cardiovascular diseases, diabetes, osteoporosis, and neurodegenerative diseases [4][5][6]. In particular, for some substances such as flavan-3-ols, the beneficial effects are not due to the compounds present in planta but rather to the related enteric metabolites. As recently reported in the literature by our group, 5-(3 ,4 -dihydroxyphenyl)-γ-valerolactone (1), which was identified as a metabolite in human urine after consumption of standardized and rich polyphenols dietary supplement [7], displays inhibition of Candida albicans adhesion.

Introduction
Plant-derived compounds have successfully inspired the drug discovery process which has exploited the entire structure of such natural products or part of that to develop new medicinal drugs [1,2].
Polyphenols and related compounds are secondary metabolites which occur naturally in plants and which have been reported to display protective effects in plant-based diet [3].
Indeed, food containing polyphenols are known to exert beneficial effects after long term consumption offering protection against the development of cancers, cardiovascular diseases, diabetes, osteoporosis, and neurodegenerative diseases [4][5][6]. In particular, for some substances such as flavan-3-ols, the beneficial effects are not due to the compounds present in planta but rather to the related enteric metabolites. As recently reported in the literature by our group, 5-(3′,4′-dihydroxyphenyl)-γ-valerolactone (1), which was identified as a metabolite in human urine after consumption of standardized and rich polyphenols dietary supplement [7], displays inhibition of Candida albicans adhesion.
A considerable amount of naturally occurring γ-alkylidenebutenolide have the Z configuration and most of them lack a β-substituent as demonstrated by compounds 3a, 3b, 4, 5a, and 5b.
Although the E-isomers are less stable than the Z-counterparts, in the absence of a βsubstituent the formation of Z-isomers remains small [11]. Therefore, traditional synthetic strategies including alkylidenation of preformed oxacycles as butanolides and 2-silyloxyfurans, to the best of our knowledge, are nonstereoselective [12]. Alternative methods offer stereochemical predictability and high level of selectivity but need stereodefined precursors, chiral ligands, or removable stereocontrol elements [13][14][15]. Since the biological activity of compounds featuring a γ-alkylidenebutenolide is due to this core, we focus our attention on preparing the 5-(3′,4′-bis(benzyloxy)benzylidene)furan-2(5H)-one via a stereocontrolled reaction (2a Z-isomer, 2b E-isomer; Scheme 1). For these reasons stereoselective preparation of γ-alkylidenebutenolide continues to be an important issue for organic chemists.
A considerable amount of naturally occurring γ-alkylidenebutenolide have the Z configuration and most of them lack a β-substituent as demonstrated by compounds 3a, 3b, 4, 5a and 5b.
Although the E-isomers are less stable than the Z-counterparts, in the absence of a β-substituent the formation of Z-isomers remains small [11]. Therefore, traditional synthetic strategies including alkylidenation of preformed oxacycles as butanolides and 2-silyloxyfurans, to the best of our knowledge, are nonstereoselective [12]. Alternative methods offer stereochemical predictability and high level of selectivity but need stereodefined precursors, chiral ligands, or removable stereocontrol elements [13][14][15]. Since the biological activity of compounds featuring a γ-alkylidenebutenolide is due to this core, we focus our attention on preparing the 5-(3 ,4 -bis(benzyloxy)benzylidene)furan-2(5H)-one via a stereocontrolled reaction (2a Z-isomer, 2b E-isomer; Scheme 1).
We decided to use tert-butyldimethylsilyltrifluoromethanesulfonate (TBDMSOTf) which serves as both silylating agent and Lewis acid catalyst. We began our investigation treating the commercially available 2(5H)-furanone with DBU either to form the intermediate 2-tert-butyldimethylsiloxyfuran (11) or to dehydrate it. After several unsatisfactory attempts in which we obtained the mixture of the E-and Z-isomers we started an insightful theoretical investigation of the possible transition states.
Encounter between the C1 and C5 atoms of the aldehyde and furan respectively could occur through the si faces or the si and re faces. Accordingly to what was reported by Jefford et al. [17], the resultant two pairs of staggered arrangements A, B and, C, D will produce the threo (12), while the other two pairs A', B' and, C', D' will lead to the formation of the erythro (13) aldols (Scheme 2). Moreover, in accordance with the vinylogous Mukayama reaction mechanism the Lewis acid TBDMSOTf coordinates the aldehyde with syn orientation. Thus, the prevalence of one arrangement over the other depends only on steric and electronic factors. The least hindered arrangements should be A and B'. Since the arrangement A is Diels-Alder like it is favored and it pushes for the threo selectivity. Scheme 1. Synthetic strategy to obtain 2a and 2b.
We decided to use tert-butyldimethylsilyltrifluoromethanesulfonate (TBDMSOTf) which serves as both silylating agent and Lewis acid catalyst. We began our investigation treating the commercially available 2(5H)-furanone with DBU either to form the intermediate 2-tert-butyldimethylsiloxyfuran (11) or to dehydrate it. After several unsatisfactory attempts in which we obtained the mixture of the Eand Z-isomers we started an insightful theoretical investigation of the possible transition states.
Encounter between the C1 and C5 atoms of the aldehyde and furan respectively could occur through the si faces or the si and re faces. Accordingly to what was reported by Jefford et al. [17], the resultant two pairs of staggered arrangements A, B and, C, D will produce the threo (12), while the other two pairs A', B' and, C', D' will lead to the formation of the erythro (13) aldols (Scheme 2). Moreover, in accordance with the vinylogous Mukayama reaction mechanism the Lewis acid TBDMSOTf coordinates the aldehyde with syn orientation. Thus, the prevalence of one arrangement over the other depends only on steric and electronic factors. The least hindered arrangements should be A and B'. Since the arrangement A is Diels-Alder like it is favored and it pushes for the threo selectivity.
The anion equivalent 10 would avoid the arrangements C and C' because the charge would be better dispersed in D and We also applied the DFT quantum mechanical calculations to further investigate the Diels-Alder-like arrangements. To simplify the calculation and to focus attention on the simulated vinylogous Mukayama aldol reaction, the tert-butyldimethylsilyl group was replaced by a methoxy group, while the benzyloxy substituents were removed.
As shown in Figure 3, the DFT quantum mechanical calculations allow to reach five main considerations: 1. The exo-conformation is slightly favored compared to the endo-conformation, although this result could be influenced by the lesser steric hindrance of the methoxy group, simulated instead of the TBDMS group for simplicity; 2. The vinylogous Mukayama aldol reaction is energetically possible, whether the intermediate assume exo or endo-conformation; Scheme 2. Encounter between the C1 and C5 atoms of the aldehyde and furan, respectively.
We also applied the DFT quantum mechanical calculations to further investigate the Diels-Alder-like arrangements. To simplify the calculation and to focus attention on the simulated vinylogous Mukayama aldol reaction, the tert-butyldimethylsilyl group was replaced by a methoxy group, while the benzyloxy substituents were removed.
As shown in Figure 3, the DFT quantum mechanical calculations allow to reach five main considerations: 1.
The exo-conformation is slightly favored compared to the endo-conformation, although this result could be influenced by the lesser steric hindrance of the methoxy group, simulated instead of the TBDMS group for simplicity; 2.
The vinylogous Mukayama aldol reaction is energetically possible, whether the intermediate assume exo or endo-conformation; 3.
The product obtained from endo-conformation is however clearly favored and this trend is already observed in the chiral intermediate. This result is very evident both in the different stability of the two final products and consequently in the different energy profile of the two reactions;

4.
Focusing on the two final products, the higher stability of the Z-isomer is clearly because only this isomer is able to assume a completely planar conformation that allows a full delocalization between the two rings.

5.
Moreover, a weak non-classical intramolecular hydrogen bond involving C'6-H'6-O1 shown in Figure 4 plays an important role in the stabilization of the Z-isomer.
3. The product obtained from endo-conformation is however clearly favored and this end is already observed in the chiral intermediate. This result is very evident both in the ifferent stability of the two final products and consequently in the different energy prole of the two reactions; 4. Focusing on the two final products, the higher stability of the Z-isomer is clearly ecause only this isomer is able to assume a completely planar conformation that allows full delocalization between the two rings. Considering these assumptions, we used DIPEA for the formation of the 2-tert-butylimethylsiloxyfuran to enhance a diastereoselectivity coming from the Diels-Alder trantion state since the use of the DBU alone allows the formation of anion 10 which would opt D and D' arrangements giving reason to the E/Z mixture formation thus a partial reo diastereoselectivity. As supposed and well explained by the Diels-Alder-like oriention of the reactants and by the quantum mechanics calculations, the use of DIPEA for e formation of 12 and DBU to eliminate the TMDMOH gave only the Z-isomer.
The obtained compound exhibited the expected spectroscopic signals ( 1 H-NMR, 13 C-MR, ESI-MS and HRMS -Supplementary Materials-) confirming the successful synthesis f Z-γ-alkylidenebutenolide 2a. Using Figure 4 as reference, the 1 H-NMR (CDCl3) spec- Considering these assumptions, we used DIPEA for the formation of the 2-tertbutyldimethylsiloxyfuran to enhance a diastereoselectivity coming from the Diels-Alder transition state since the use of the DBU alone allows the formation of anion 10 which would adopt D and D' arrangements giving reason to the E/Z mixture formation thus a partial threo diastereoselectivity. As supposed and well explained by the Diels-Alder-like orientation of the reactants and by the quantum mechanics calculations, the use of DIPEA for the formation of 12 and DBU to eliminate the TMDMOH gave only the Z-isomer.
The obtained compound exhibited the expected spectroscopic signals ( 1 H-NMR, 13 C-NMR, ESI-MS and HRMS in the Supplementary Materials) confirming the successful synthesis of Z-γ-alkylidenebutenolide 2a. Using Figure 4 as reference, the 1 H-NMR (CDCl 3 ) spectrum shows confirmatory assignments accordingly to Chang et al. [18] such as the doublet and the singlet integrating as one hydrogen each for H3 and H6 (6.15 d, J = 5.3 Hz and 5.91 s, 1H).
The reaction paths were monitored by simulating the involved reactants and products at their ground-state and at gas phase by density functional theory (DFT) using the Becke three-parameter hybrid function with LYP correlation (DFT/B3LYP) and with the 6-31G basis set as implemented by the GAMESS software [19].
The MS analysis was performed on a TSQ Quantum Ultra Triple Quadrupole (Ther-moFinnigan Italy, Milan, Italy) equipped with an ESI source. The following source parameters were used: positive ion mode, capillary temperature 275 • C, spray voltage 4 kV, capillary voltage 33 V, tube lens voltage 120 V. The flow rate of the nebulizer gas (nitrogen) was 10 a.u. The mass spectrometer acquired in full mass scan and the Q3 was used as detector with a scan range 200-700 m/z. The HRMS analysis was performed on a LTQ Orbitrap XL (Thermo Scientific, Bremen, Germany) equipped with an ESI source. The following source parameters were used: positive ion mode, capillary temperature 275 • C, spray voltage 4 kV, capillary voltage 30 V, tube lens offset 90 V. The flow rate of the nebulizer gas (ni-trogen) was 10 a.u. The mass spectrometer acquired in full mass scan, with a scan range of 200-600 m/z and resolution 30,000 FWHM at m/z 400. DIPEA (0.27 mL, 1.53 mmol) was added under nitrogen atmosphere to a solution of 2(5H)-furanone (42.88 mg, 0.51 mmol) in dry THF (3.5 mL). The mixture was stirred for 30 min at room temperature, and after cooling down to −10 • C, tert-butyldimethylsilyltrifluoromethanesulfonate (0.13 mL, 0.56 mmol) and 3,4-bis(benzyloxy)benzaldehyde (141.0 mg, 0.56 mmol) were added dropwise. The mixture was stirred for 2 h at the same temperature and subsequently 2 equivalents of DBU (0.15 mL, 1.02 mmol) were added. The reaction mixture was stirred overnight at room temperature, then solvent was removed under vacuum. Ethyl acetate (20 mL), EtOH (5 mL) and saturated solution of sodium bisulfite (5 mL) were added to the crude residue and stirred overnight at 40 • C. The phases were separated, and the organic layer was diluted with ethyl acetate (15 mL), treated with 2.9 N HCl (3 × 20 mL), washed with brine (20 mL), dried and concentrated to afford a sticky black oil. The crude product was purified on silica gel (75:25 cyclohexane/ethyl acetate) to afford the title compound as an orange oil (100.0 mg, 0.26 mmol, 52% yield). 1 13