Streptopyridines, volatile pyridine alkaloids produced by Streptomyces sp. FORM5

Introduction

Actinomycetes are excellent producers of diverse and bioactive secondary metabolites. These metabolites belong to many different structural classes including polyketides, nonribosomal peptides, terpenoids, alkaloids, lipids and others. Such compounds became a major source of biologically active natural products as antibiotics, cytotoxic compounds, immunosuppressants etc. In addition, actinomycetes are also able to produce and release a wide variety of volatile compounds with bouquets composed of up to 100 different compounds [1-6]. Major volatile classes comprise aliphatic compounds derived from fatty acid metabolism, terpenes, aromatic compounds, sulfur compounds, and pyrazines [1]. Apart from pyrazines, indole, and a few strain specific compounds [2] such as methyl pyrrole-2-carboxylate, emitted by Stackebrandtia nassauensis, or 2-acetylpyrrole from Saccharopolyspora erythraea, volatile alkaloids are rarely produced by actinomycetes.

We became interested in the strain Streptomyces sp. FORM5 to elucidate whether volatile formation is linked to the production of other, usually less volatile secondary metabolites and whether different compounds can be detected by headspace analysis [7] compared to commonly used solvent extraction or adsorption/extraction procedures. Strain FORM5 has been reported to produce the tetrahydrocyclopenta[b]pyridine derivatives streptazones B₁ (1), B₂ (2), C (3), the 4-pyridone derivative streptazone D (4) with a pentadienyl side chain, and streptazolin (5) (Figure 1) [8]. Streptazolin is produced by several streptomycetes [8-12], and is formed biosynthetically by a polyketide mechanism [13]. The respective polyketide synthase gene cluster has not been identified yet.

The streptazones are relatively small compounds suggesting that they may be volatile enough to find them in the headspace above bacterial cultures, although the presence of hydrogen bond donor and acceptor sites hints to good solubility in the aqueous phase.

In our study the volatile bouquet of the actinomycete Streptomyces sp. FORM5 was investigated and several new 2-alkylated pyridines were identified using the closed-loop stripping analysis (CLSA) [7] headspace technique followed by GC–MS analysis and synthesis of the target compounds for structure verification. Agar plate cultures and liquid cultures were investigated and the liquid phase analyzed for the presence of secondary metabolites. The results showed that by headspace analysis new secondary metabolites can be found that eluded earlier analysis. The separate analysis of headspace and liquid phase is complementary and in combination allows better evaluation of the metabolic potential of an investigated microorganism.

Results and Discussion

The volatiles released by agar plate cultures of strain Streptomyces sp. FORM5 were collected by CLSA for one day on a charcoal filter and eluted with dichloromethane. The extract was then analyzed using GC–MS. More than 40 different compounds were identified in the headspace extract (Table 1, Figure 2, and Figure S1 in Supporting Information File 1). Nevertheless, the major compounds (compounds 8, 9, 11, and 12 in Figure 2) attracted our interest, because they were unknown, thus giving room for the discovery of new volatile secondary metabolites. High resolution GC–MS revealed a molecular composition of C₁₀H₁₁N (found 145.09136, calcd 145.08910) for the major compound 12 and C₁₀H₁₃N (found 147.10428, calcd 147.10475) for the minor component 8. The mass spectrum (Figure 3) of the major compound pointed to the presence of an extended aromatic and conjugated π-system and the formation of a stable [M − 1]⁺ ion. The methyl loss to form the base peak [M − 15]⁺ indicated the presence of a methyl group in the compound. Careful analysis of the extract revealed that a small peak (7) eluted slightly earlier than compound 8. The mass spectrum of compound 7 matched that of 2-pentylpyridine, present in public databases [14]. From these data we concluded that the unknown compound 12 might be a 2-(pentadienyl)pyridine with conjugated side chain and that the compounds 9–12 might be diastereomers. Compound 8 should carry a pentenyl side chain, while compound 6 showed a mass spectrum identical to the known one of 2-propylpyridine.

The target compounds were then synthesized to prove the structural proposal. Pentadienylpyridines 9–12 were synthesized by Wittig reaction using different conditions (Scheme 1). A Wittig–Schlosser reaction [15] starting from a commercially available 5:1 E/Z-mixture of 1-bromobut-2-ene (17) led to preferentially (1E)-configured products. After conversion of 17 into the respective Wittig salt 18 and reaction with 2-pyridinecarbaldehyde (19) a mixture of four diastereoisomers of 2-(1,3-pentadienyl)pyridine was formed (Figure 4), all showing similar mass spectra. These four diastereomers proved to be identical to the natural compounds 9 to 12 by comparison of mass spectra and GC retention. The major compound, 2-((1E,3E)-penta-1,3-dienyl)pyridine (12), and the 1Z,3E-isomer 9 could be isolated in almost pure form, but a large amount of material was lost during the purification process (17% yield for compound 12 and 3% yield for compound 9 after purification). The large coupling constants ³J around 15 Hz between H-1 and H-2 (15.8 Hz) as well as H-3 and H-4 (15.1 Hz) in the side chain indicated the E-configuration of both double bonds for compound 12. The mass spectrum and retention time proved to be identical to compound 12, the major compound of the natural extract. We propose the name streptopyridine A for this new natural compound. The minor product isolated pure under these conditions was 2-((1Z,3E)-penta-1,3-dienyl)pyridine (9, streptopyridine B), indicated by the coupling constants ³J_1,2 = 11.8 Hz and ³J_3,4 = 15.1 Hz.

To delineate the stereochemistry of the other two isomers 10 and 11, the conditions of the Wittig reaction were changed to favor Z-configured products by using NaHMDS as base. Again, all four diastereomers were formed (Figure 4). Together with knowledge of the structures of 9 and 12, the product ratio in the Z-selective reaction indicates that compound 10 (streptopyridine C) is 2-((1Z,3Z)-penta-1,3-dienyl)pyridine, while compound 11 is 2-((1E,3Z)-penta-1,3-dienyl)pyridine (streptopyridine D): The formation of only small amounts of 11 indicates that this compound is 1E,3Z-configured, because it is disfavored by the 1Z-selective reaction conditions and the minor amounts of the Z-configured isomer in the diastereomeric mixture of Wittig salts. Conclusively, 10 must be the last possible 1Z,3Z-stereoisomer. Both compounds 10 and 11 could not be isolated in pure form, but their mass spectra and retention times were identical to those of the natural products.

The mass spectrum of compound 8 indicated that the side chain contained only one double bond, the position of which had to be determined. A 1-pentenyl side chain seemed unlikely because of the high abundance of the m/z 93 ion in the mass spectrum of 8, which we assumed is a McLafferty ion that is commonly observed in 2-alkylpyridines [16]. Basing on the structure of streptopyridine A, a 3-pentenyl side chain seemed to be most likely. Coupling of (E)-3-pentenylmagnesium bromide with 2-chloropyridine under Fürstner conditions with iron(III) acetylacetonate as catalyst [17] yielded (E)-2-(pent-3-enyl)pyridine (8) that proved to be identical to the natural compound, now called streptopyridine E. The mass spectra of 2-(pent-1-enyl)pyridine and 2-(pent-2-enyl)pyridine, compounds synthesized for comparison, are shown in Supporting Information File 1 and differ from that of 8. Finally, pyridines 6 and 7 were synthesized also by Fürstner cross-coupling and proved to be identical to the natural products.

2-Alkylpyridines have been reported earlier as aroma components, like 2-butylpyridine or 2-pentylpyridine (7) identified in fried chicken [18], or 2-propylpyridine (6), present in sesame seed oil [19], but are not known from bacteria. Natural products of bacteria containing a pyridine ring are rare. As an example, 1-(2-pyridinyl)ethanone was identified as a volatile of Enterobacter agglomerans [20]. Highly substituted pyridine derivatives can be found in bacterial thiopeptide antibiotics [21].

The streptopyridines of Streptomyces sp. FORM5 are structurally related to known secondary metabolites by Streptomyces. The piperidine derivatives 2-((1E,3E)-1,3-pentadienyl)piperidine (20) and 2-((1E,3E)-1,3-pentadienyl)piperidin-4-ol (SS20846A, 21, Figure 5) have been reported from other streptomycetes [8,22,23]. They constitute hydrogenated analogs of the streptopyridines and occur together with streptazolin (5).

We then tested whether the streptopyridines can also be detected under conventional cultivation and isolation procedures. Therefore, strain FORM5 was grown as liquid culture. Headspace analysis revealed the production of the streptopyridines also under these conditions. The liquid cultures were either extracted with ethyl acetate (E-extract) or filtered over Oasis adsorption material. The latter was than extracted with ethyl acetate (O-extract). These extracts were analyzed by GC–MS. While the E-extract did not show the presence of any streptopyridine, they were present as trace components in the O-extract. Both extracts showed two major constituents, one with a molecular mass of 151 u (C₁₀H₁₇N, HRMS found 151.13656, calcd 151.13605), and the other with a molecular mass of 207 u (C₁₁H₁₃NO₃, HRMS found 207.09056, calcd 207.08949). Although the compounds were not isolated, the mass spectral data and the previous reports of this class of compounds from Streptomyces led us to conclude that these compounds are indeed streptazolin (5, molecular mass 207) and 2-(penta-1,3-dien-1-yl)piperidine (20, molecular mass 151, mass spectra and high resolution data see Supporting Information File 1). Both compounds are accompanied by diastereomers exhibiting the same mass spectrum but different retention times. Minor components of the extracts could be tentatively assigned by their mass spectra to be the hydroxypiperidine 21, occurring again as a pair of diastereomers, and streptazone D (4). The mass spectrum of 4 matches the published data [8]. Streptazone B₁/B₂ and/or C elute as broad peak from the GC column; a discrimination basing on the mass spectrum is not possible.

Several additional N-containing compounds occur in the extracts, some of them can be tentatively identified basing on their mass spectra. Two compounds exhibiting a small molecular ion at m/z 153 and a dominating base peak at m/z 84 are likely 2-(3-pentenyl)piperidines (22, mass spectrum see Supporting Information File 1). The ion m/z 84 is typical for 2-alkylpiperidines [24] and cannot be formed in piperidine 20 because of the adjacent double bond. The 3-pentenyl side chain is also supported by a small ion series at m/z 94 and 108 and present in streptopyridine E (8) and streptenols A (28) and B, biosynthetic precursors of this compound family (see below). Another compound, only present in the O-extract exhibits a molecular mass of 149 u, 2 units less than the major compound 20. The mass spectrum (see Supporting Information File 1) resembles that of 20. The additional double bond resides most likely at the nitrogen, arriving at the 1-piperideine structure 24. A similar structure has the antibiotic nigrifactin (26), a hexaketide produced by S. nigrifaciens, differing only in the length of the side chain [25]. Piperideine 24 lacks a N–H and might get lost during work-up of the E-extract, contrary to the other alkylpiperidines. It can be detected as trace component in the headspace extract as well (see Table 1). As with piperidines 20 and 21, a hydroxypiperideine 25 seems to be present (Figure 5, mass spectrum see Supporting Information File 1). Its oxidation product is streptazone D (4) in which the ring double bond moves into conjugation with the carbonyl group by imine–enamine tautomerisation. Finally compound 23 is produced, a derivative of piperidine 21 with an additional hydroxy group with unknown location in the ring. Compounds 22–25 (Figure 5) as well as the streptazolin isomer have not been reported from nature before.

We then tested whether the streptopyridines are biosynthetically produced via a polyketide sequence similar to that reported for streptazolin, involving a pentaketide precursor [13], or whether a specific pyridine precursor, e.g., pipecolic acid, with chain elongation was used. Feeding experiments with ¹³C₂-sodium acetate showed incorporation of up to five acetate units by GC–MS, indicated by a mass shift of 10 amu for the molecular ion, from m/z 145 to m/z 155 (Figure 6a and 6b). Because of the dilution with unlabelled acetate the ¹³C₁₀ isotopomer is of low abundance (Figure 6c). Nevertheless, the dose dependent incorporation of the acetate units clearly showed the presence of this isotopomer. Feeding of 2 mM sodium ¹³C₂-acetate to agar plate cultures showed double incorporation compared to 1 mM sodium ¹³C₂-acetate (Figure 6d). The results hint to a biosynthesis of the streptopyridines via the polyketide pathway.

The proposed biosynthesis of the streptopyridines is shown in Scheme 2. The streptopyridines might be as well as the streptazones, streptenols (27) and piperidinols (20, 21) [8,9] precursors or side products in the biosynthesis of streptazolin (5) [8]. The biosynthesis of 5 has been investigated earlier [13]. Mayer and Thiericke proposed a pentaketide precursor 34 that is transformed into the amine 33. This amine is N-carboxylated, cyclized, and further processed to form 5 [13].

The streptopyridines might similarly be formed from the pentaketide 29, showing the reduction status occurring in the previously isolated streptenols A and C (27) [9]. Reduction and transamination leads to the amine 30 that cyclizes to the piperideine 25. Elimination of water leads to the dihydropyridine 31 that is oxidized to the major streptopyridine 12 possibly by spontaneous autoxidation in air. Isomerization of the double bonds during this pathway may lead to the isomers 9–11. Reduction of 25 would lead to piperidine SS 20846A (21) [9,23]. Oxidation of intermediate 25 can also form streptazone D (4) by oxidation which would concomitantly shift the double bond into conjugation to the carbonyl group. Reductive removal of the hydroxy group, e.g., via 31 followed by double bond reduction may lead to piperideine 24, a precursor of the major liquid phase component 22. Alternatively, this compound might originate from the reduced PKS precursor 32 that is transformed via 33 into 24. Piperidine 22 is then obtained via imine reduction as described. On the other hand, this pathway may also be the entry into the streptopyridine formation by oxidation of 24 to, e.g., 31, followed by final oxidation.

A 3-pentenyl side chain as found in streptopyridine 8 and other derivatives occurs also in streptenol A (28), isolated from S. luteogriseus FH-S 1307 [9], S. fimbriatus [26], S. cirratus [27], and Streptomyces sp. HS-HY-045 [28]. This might indicate that the double bond hydrogenation occurs already during the pentaketide biosynthesis in these cases. Similarly, additional hydrogenation leads to the saturated alkylpyridine 7 and a tetraketide to propylpyridine (6).

In the bouquet of the headspace extract of Streptomyces strain FORM5 several other compounds besides the pyridines 6–12 were identified (Figure 7, Table 1). The most abundant of these were dimethyl disulfide (35), accompanied by other sulfur components as dimethyl trisulfide (36), dimethyl tetrasulfide (37), and S-methyl methanethiosulfonate (50). The hydroxyketones acetoin (40), and longer variants 38, 39, 41, and 42 occur often in bacteria and are precursors of alkylated pyrazines [29] like 2,5-dimethylpyrazine (44). Aldehydes, ketones, and aromatic compounds commonly found as volatiles from bacteria were present in trace amounts: 5-hepten-2-one (43), 2-acetylfuran (45), 3-octanone (48), nonanal (54), decanal (55), 1-phenyl-2-propanone (57), 1-phenyl-1,2-propandione (59), benzaldehyde (46), methyl benzoate (51), 2-phenylethanol (56), 1-phenyl-2-propanol (58), ethyl benzoate (52), and methyl 2-phenylacetate (53) [2]. Of special interest is 5-hepten-2-one (43) that may be a shunt product of the streptopyridine E biosynthesis: It contains a 3-pentenyl chain motif adjacent to a carbonyl group, thus resembling the structural requirements of a possible streptopyridine E biosynthesis that follows the logic as presented in Scheme 2. Cyclohept-4-enone (49) has recently been reported from several actinomycetes [2]. Some terpenes could be identified as well. 2-Methylisoborneol (60) and geosmin (62) are commonly produced by Streptomyces and other actinomycetes [3,30]. In addition, the sesquiterpene valencene (63) was found, but the amount of terpenes released is quite low compared to other streptomycetes. Some nitrogen containing trace components could not be identified. In the E- and O-extracts similarly other nitrogen containing trace components occurred, although the small amounts excluded their identification.

The streptopyridines showed only weak antibacterial and cytostatic activity (R. Müller, pers. commun.), similar to that described earlier by us for 2-pentylpyridine [31]. The analysis of the 16S-RNA revealed strain FORM5 to be a Streptomyces. It showed 99% sequence similarity to Streptomyces griseosporus (R. Müller, pers. commun.).

The two analytical methods used in the current work are obviously orthogonal to each other. They can be used on the same culture. After initial sampling of the headspace of a liquid culture, the culture can be separated from the cells and extracted as described. This consecutive approach allows a broad overview on the metabolites. The E- or O-extracts can be analyzed by HPLC–MS and GC–MS. Small, basic compounds as the piperidines are released from the liquid medium and can be detected only by the extraction methods. Their basicity and/or their ability to interact by hydrogen bonding with water obviously prevent release from the water phase in substantial amounts. Volatile compounds like the streptopyridines are less soluble, have a lower basicity and can be detected as major compounds in the headspace. Both analytical methods have a different analytical window and complement each other.

The detected volatiles fall into different groups. Most of the compounds listed in Table 1 can be regarded as volatiles commonly produced by various bacteria. That does not imply that most bacteria release them, but that these volatiles often occur when bacteria are analyzed. These compounds form a chemical structure space of volatiles released by bacteria and their number is limited, although this space is certainly only partially explored. Another group of volatile compounds forming a structure space is already known from the green part of plants (excluding flowery parts). The plant structure space is different from that emerging for bacteria. The bacterial structure space includes acetoins and aromatic aldehydes, esters and ketones, aliphatic compounds, sulfur compounds, but also 4-cycloheptenone that we found in several other bacteria (unpublished results). The terpenes geosmin and methylisoborneol are typical terpenes of the actinomycetes. Various sesquiterpene cyclases occur in the streptomycetes [3,30,32] and give rise to a wide variety of sesquiterpenes, in this case valencene.

The only strain specific compounds are the streptopyridines. They have not been reported from other strains and their biosynthesis seems tightly connected to the biosynthesis of streptazolin. A similar case has been reported for specific volatile butenolides released by streptomycetes producing the antibiotic antimycin [33] and for other strains investigated by us. The analysis of volatiles and detection of unique compounds may thus be used as a method to select microbial strains for the detection of non-volatile biologically active compounds. Alternatively, two independent gene clusters may be responsible for streptazolin and streptopyridines.

The production of strain specific compounds connected to, e.g., antibiotic biosynthesis might also have important ecological consequences. As an example, streptazolin producing streptomycetes have been isolated from mud-dauber wasps [34]. They have been postulated as antibiotic-producing symbionts of the wasps. If this is true, they should also produce specific volatiles as the streptopyridines and add to the odor of the insect. Given the many different bacteria living on the insect, a specific odor bouquet of the insect would arise, assembled by insect derived compounds and bacterial volatiles, finally carrying information on the individual symbiont composition. The symbiont composition might affect the fitness and, if it can be perceived by interacting partners, may in the end influence the behavior of the insects, e.g., mate choice or aggression.

Conclusion

In conclusion, the investigation of the headspace extract of Streptomyces strain FORM5 revealed the occurrence of new 2-alkylpyridines that are structurally related to streptazolin and 2-pentadienylpiperidines produced by this strain. While they are the major compounds in the volatile bouquet, they occur only in minor amounts in the liquid phase. In contrast, the major compounds streptazolin and 2-pentadienylpiperidine do not occur in the headspace, thus proving the necessity to use orthogonal analytical methods to assess the full metabolic potential of a microorganism.

Experimental

General experimental procedures

Reagents and solvents were purchased from Sigma-Aldrich Chemie GmbH (Steinheim, Germany) and Acros Organics (Geel, Belgium) and used without further purification. Solvents were distilled before use and, if necessary, dried using standard procedures. All non aqueous reactions were performed under an inert atmosphere (N₂) in flame-dried flasks. Purification of the synthetic products was carried out by flash chromatography using Merck silica gel 60 (70–200 mesh). Thin-layer chromatography was performed with 0.2 mm pre-coated polyester sheets (Polygram SIL (G/UV254), Macherey-Nagel). NMR spectra were obtained on either a Bruker DRX-400 (400 MHz) or an AV III-400 (400 MHz) spectrometer and were referenced against TMS (δ = 0.00 ppm) for ¹H NMR and CHCl₃ (δ = 77.16 ppm) for ¹³C NMR. GC–MS analysis were performed on an Agilent 7890A gas chromatograph connected to an Agilent 6975 C inert mass detector fitted with a BPX-5 fused silica capillary column (25 m, 0.25 mm i.d., 0.25 μm film). Conditions were as follows: inlet pressure 67 kPa, He 23.3 mL/min, injection volume 1 µL, transfer line 300 °C, injector 250 °C, electron energy 70 eV. The gas chromatograph was programmed as follows: 5 min at 50 °C, then increasing with 5 °C/min to 320 °C. Linear retention indices were determined from a homologous series of n-alkanes (C8–C32). Compounds were identified by comparison of mass spectra to database spectra (Wiley 7, NIST 08 and our own created from synthesized reference compounds), by comparison of the retention index data to standards (own database and NIST Chemistry WebBook (2013) [14]) and by synthesis of reference compounds.

Organism and analysis

Streptomyces strain FORM5 was isolated from a soil sample collected in Formentera (Spain) and is deposited at the Institute of Organic Chemistry in Göttingen [8]. It was cultivated in 10 mL SM-media (20 g/L mannitol, 20g/L soy flour, 4 mL/L 2.5 M magnesium chloride solution, 20 g/L agar only for plates) at 28 °C for 3 days. SM-agar plates were then inoculated with 300 µL of the preculture and cultivated for 6 days at 28 °C. Then the culture was analyzed by closed-loop stripping analysis at room temperature [7]. In this system, air is continuously pumped (MB-21E, Senior Flextronics, USA) through the closed system that contains an activated charcoal filter (Chromtech GmbH, Idstein, Precision Charcoal Filter, 5 mg) and the agar plate or liquid culture for 24 hours. The filter was then extracted by rinsing 3× with 15 µL dichloromethane (≥99.8%, Merck, Germany) and the resulting headspace extract was analyzed by GC–MS. The experiment was repeated at least three times. The SM-medium was analyzed without inoculation as control. Liquid cultures were analyzed similarly by the CLSA method. After the collection of volatiles the liquid phase was analyzed by two different methods. E-extract: The culture media was centrifuged for 20 min at 4 °C and the supernatant was extracted 3 times with 50 mL CH₂Cl₂. The extracts were dried with MgSO₄, concentrated under reduced pressure and analyzed by GC–MS. O-extract A Oasis^® HLB cartridge (Waters) was prewashed with 2 column volumes ethyl acetate and conditioned with 2 column volumes water. The culture media was centrifuged for 20 min at 4 °C and the supernatant (100 mL) filtered through the cartridge. The cartridge was extracted with 3 column volumes ethyl acetate, the eluent was dried with MgSO₄, concentrated under reduced pressure, and finally subjected to GC–MS analysis. For feeding experiments on the biosynthesis of compound 7 the SM-media was enriched with sodium ¹³C₂-acetate (ISOTEC) in 1 mM (1.7 mg, 0.02 mmol, in 20 mL medium) and 2 mM (3.4 mg, 0.04 mmol, in 20 mL medium) followed by collection of the volatiles by CLSA.

Synthesis of reference compounds

The compounds 6–8 were synthesized after the standard procedure for iron-catalyzed aryl–alkyl cross-coupling described by Fürstner et al [17].

2-Propylpyridine (6): Yield (1.01 g, 8.35 mmol, 61%); R_f (pentane/Et₂O 5:1) 0.2; UV (CH₂Cl₂) λ_max (log ε): 257 (5.77), 262 (5.78) nm; IR (diamond) ν_max: 2960, 2832, 2871, 1590, 1569, 1472, 1434, 1149, 1051, 993, 751 cm⁻¹; ¹H NMR (CDCl₃, 400 MHz) δ ppm 0.97 (t, J = 7.4 Hz, 3H, CH₃), 1.76 (sxt, J = 7.5 Hz, 2H, CH₂), 2.74–2.79 (m, 2H, CH₂), 7.07–7.11 (m, 1H, CH), 7.14 (dd, J = 7.8, 0.5 Hz, 1H, CH), 7.58 (tdd, J = 7.6, 1.9, 0.9 Hz, 1H, CH), 8.52 (dt, J = 4.89, 0.94 Hz, 1H, CH); ¹³C NMR (CDCl₃, 100 MHz) δ ppm 13.8 (CH₃), 23.1 (CH₂), 40.4 (CH₂), 120.8 (CH), 122.7 (CH), 136.1 (CH), 149.2 (CH), 162.3 (C); EIMS m/z: 121 [M]⁺ (2), 120 (9), 106 (29), 93 (100), 78 (12), 65 (18), 51 (15), 39 (18); HREIMS m/z: calcd for C₈H₁₁N, 121.0891; found, 121.0888; GC (BPX-5) I = 1001.

2-Pentylpyridine (7): Yield (827 mg, 5.6 mmol, 56%); R_f (pentane/Et₂O 5:1) 0.2; UV (CH₂Cl₂) λ_max (log ε): 257 (6.28), 262 (6.29) nm; IR (diamond) ν_max: 2955, 2928, 2858, 1590, 1472, 1434, 1148, 993 cm⁻¹; ¹H NMR (CDCl₃, 400 MHz) δ ppm 0.86–0.93 (m, 3H, CH₃), 1.29–1.40 (m, 4H, 2× CH₂), 1.68–1.78 (m, 2H, CH₂), 2.74–2.82 (m, 2H, CH₂), 7.08 (ddd, J = 7.5, 4.9, 1.1 Hz, 1H, CH), 7.13 (dd, J = 7.8, 1.0 Hz, 1H, CH), 7.53–7.60 (m, 1H, CH), 8.50–8.55 (m, 1H, CH); ¹³C NMR (CDCl₃, 100 MHz) δ ppm 13.9 (CH₃), 22.5 (CH₂), 29.5 (CH₂), 31.5 (CH₂), 38.4 (CH₂), 120.7 (CH), 122.6 (CH), 136.1 (CH), 149.1 (CH), 162.5 (C); EIMS m/z: 149 [M]⁺ (2), 93 (100), 120 (25), 106 (30), 92 (14), 78 (14), 65 (16), 51 (10), 39 (14); HREIMS m/z: calcd for C₁₀H₁₅N, 149.1204; found, 149.1203; GC (BPX-5) I = 1205.

2-((E)-Pent-3-en-1-yl)pyridine (8): Yield (326 mg, 2.2 mmol, 16%); R_f (pentane/Et₂O 5:1) 0.24; UV (CH₂Cl₂) λ_max (log ε): 257 (5.73), 262 (5.74) nm; IR (diamond) ν_max: 3009, 2918, 2854, 1590, 1569, 1474, 1434, 1148, 1051, 966, 750 cm⁻¹; ¹H NMR (CDCl₃, 400 MHz) δ ppm 1.62–1.64 (m, 3H, CH₃), 2.38–2.44 (m, 2H, CH₂), 2.82–2.85 (m, 2H, CH₂), 5.41–5.52 (m, 2H, 2× CH), 7.07–7.10 (m, 1H, CH), 7.13 (d, J = 7.8 Hz, 1H, CH), 7.57 (td, J = 7.6, 1.9 Hz, 1H, CH), 8.51–8.53 (m, 1H, CH); ¹³C NMR (CDCl₃, 100 MHz) δ ppm 17.5 (CH₃), 32.4 (CH₂), 38.1 (CH₂), 120.6 (CH₂), 122.4 (CH₂), 125.2 (CH), 129.9 (CH), 135.8 (CH), 148.8 (CH), 161.4 (C); EIMS m/z: 147 [M]⁺ (17), 146 (29), 133 (11), 132 (100), 119 (17), 118 (30), 117 (47), 106 (25), 93 (77), 79 (17), 78 /14), 65 (18), 51 (13), 39 (19); HREIMS m/z: calcd for C₁₀H₁₃N, 147.1048; found, 147.1054; GC (BPX-5) I = 1208.

The synthesis of compounds 9 and 12 was achieved by Wittig reaction starting with the synthesis of crotyltriphenylphosphonium bromide (18). Crotyl bromide (17, 2.23 g, 16.52 mmol) was added to a mixture of triphenylphosphine (3.67 g, 14 mmol) in THF and stirred under reflux overnight. THF was removed under reduced pressure and the resulting solid was dissolved in a mixture of CH₂Cl₂/MeOH (10:1). Column chromatography on silica gel with CH₂Cl₂/MeOH (15:1, R_f = 0.25) yielded 18 (5.12 g, 12.9 mmol, 92%) as a white solid. ¹H NMR (CDCl₃, 200 MHz) δ ppm 1.35–1.42 (m, 3H, CH₃), 1.58–1.65 (m, 3H, CH₃), 4.54–4.69 (m, 4H, 2× CH₂), 5.24–5.39 (m, 2H, 2× CH), 5.87–6.04 (m, 2H, 2× CH), 7.65–7.92 (m, 30H, 30× CH); ¹³C NMR (CDCl₃, 50 MHz) δ ppm 18.1 (CH₃), 18.2 (CH₃), 27.2 (CH₂), 28.2 (CH₂), 114.6 (CH), 114.8 (CH), 117.0 (3× C), 118.7 (3× C), 130.0 (6× CH), 130.3 (6× CH), 133.6 (6× CH), 133.8 (6× CH), 134.8 (3× CH), 134.9 (3× CH), 137.4 (CH), 137.7 (CH); ³¹P NMR (CDCl₃, 80 MHz) δ ppm 21.4 (s), 21.6 (s). At room temperature an ethereal phenyllithium solution (1.63 mL, 15.5 mmol) was added to a mixture of 18 (6.15 g, 15.5 mmol) in 30 mL dry THF and 45 mL dry diethyl ether. After stirring for 20 min at rt the mixture was cooled down to −78 °C and pyridine-2-carbaldehyde (19, 1.66 g, 15.5 mmol) was added. Afterwards the mixture was allowed to warm to −30 °C in 2 h and again phenyllithium solution (1.63 mL, 15.5 mmol) was added. Then the mixture was cooled down again to −78 °C and potassium tert-butoxide (2.61 g, 23.25 mmol) was added. Overnight the mixture was allowed to warm to rt and quenched with dest. water. The aqueous layer was extracted two times with diethyl ether. The combined organic layers were dried with MgSO₄ and the solvent was removed under reduced pressure. Column chromatography on silica gel with pentane/diethyl ether (5:1) yielded 9 (0.36 mmol, 53 mg, R_f = 0.3, 3%) and 12 (2.22 mmol, 322 mg, R_f = 0.25, 14%) as yellow oils (crude yield was 62%).

2-((1Z,3E)-Penta-1,3-dien-1-yl)pyridine (9): UV (CH₂Cl₂) λ_max (log ε): 271 (6.66), 300 (6.71), 308 (6.72) nm; IR (diamond) ν_max: 3006, 2962, 2911, 1641, 1582, 1558, 1469, 1431, 1149, 990, 833, 797, 741 cm⁻¹; ¹H NMR (CDCl₃, 400 MHz) δ ppm 1.85 (dd, J = 6.8, 1.7 Hz, 3H, CH₃), 5.96 (dq, J = 15.2, 6.8 Hz, 1H, CH), 6.23 (d, J = 11.8 Hz, 1H, CH), 6.34 (dd, J = 11.5, 11.2 Hz, 1H, CH), 7.07 (dd, J = 7.5, 5.0 Hz, 1H, CH), 7.21 (d, J = 7.9 Hz, 1H, CH), 7.40 (dd, J = 15.2, 11.0 Hz, 1H, CH), 7.61 (td, J = 7.7, 1.9 Hz, 1H, CH), 8.60–8.62 (m, 1H, CH); ¹³C NMR (CDCl₃, 100 MHz) δ ppm 18.5 (CH₃), 121.0 (CH), 124.1 (CH), 125.5 (CH), 128.8 (CH), 134.1 (CH), 135.2 (CH), 136.0 (CH), 149.3 (CH), 156.9 (C); EIMS m/z: 145 [M]⁺ (9), 144 (12), 143 (6), 142 (5), 131 (10), 130 (100), 117 (5), 103 (4), 89 (3), 78 (5), 77 (4), 65 (3), 51 (4), 39 (3); HREIMS m/z: calcd for C₁₀H₁₃N, 145.0892; found, 145.0912; GC (BPX-5) I = 1334.

2-((1E,3E)-penta-1,3-dien-1-yl)pyridine (12): UV (CH₂Cl₂) λ_max (log ε): 272 (6.55), 300 (6.60), 308 (6.61) nm; IR (diamond) ν_max: 3008, 2962, 2911, 1644, 1582, 1561, 1467, 1429, 1145, 989, 796, 755, 740 cm⁻¹; ¹H NMR (CDCl₃, 400 MHz) δ ppm 1.82 (dd, J = 6.8, 2 Hz, 3H, CH₃), 5.96 (dq, J = 15.7, 6.8 Hz, 1H, CH), 6.26 (dd, J = 15.1, 10.8 Hz, 1H, CH), 6.48 (d, J = 15.8 Hz, 1H, CH), 7.04 (dd, J = 7.5, 5.0 Hz, 1H, CH), 7.21 (dd, J = 15.1, 11.3 Hz, 1H, CH), 7.21 (d, J = 7.8 Hz, 1H, CH), 7.66 (td, J = 7.7, 1.9 Hz, 1H, CH), 8.51–8.53 (m, 1H, CH); ¹³C NMR (CDCl₃, 100 MHz) δ ppm 18.3 (CH₃), 121.3 (CH), 121.4 (CH), 128.9 (CH), 131.3 (CH), 133.0 (CH), 133.2 (CH), 136.1 (CH), 149.3 (CH), 155.8 (C); EIMS m/z: 145 (18) [M]⁺, 144 (14), 143 (6), 142 (5), 131 (10), 130 (100), 117 (6), 103 (4), 78 (5), 77 (4), 65 (3), 51 (5), 39 (3); HREIMS m/z: calcd for C₁₀H₁₃N, 145.0892; found, 145.0912; GC (BPX-5) I = 1368.