Biosynthesis and Biomimetic Synthesis of Flavonoid Diels-Alder Natural Products

Abstract

This chapter describes the biosynthesis and biomimetic synthesis of naturally occurring flavonoid Diels‐Alder adducts found either from the family Moraceae or Zingiberaceae. The main topics addressed are biosynthetic studies by employing Morus alba L. cell cultures through feeding experiments of various exogenous substrates and putative precursors, as well as a various biomimetic approach for the chemical syntheses of flavonoid Diels‐Alder natural products.

1. Introduction

The flavonoid Diels‐Alder natural products are mainly found from the families of Moraceae and Zingiberaceae. Since the majority of these compounds are discovered from the Moraceae, they are often referred as mulberry Diels‐Alder flavonoids or mulberry Diels‐Alder type adducts. These secondary metabolites exhibit promising biological activities against hypertension, HIV, tuberculosis, anti‐inflammation and cancers [1–7]. Thus far, more than 140 of these Diels‐Alder type flavonoids have been discovered from nature (Figure 1). The structural complexity and promising bioactivities of these flavonoid Diels‐Alder natural products have stimulated research interest into their biosynthesis and chemical synthesis.

Figure 1.

Examples of flavonoid Diels‐Alder natural products.

The Diels‐Alder type flavonoids are considered to be formed through an enzymatic Diels‐Alder reaction between a dehydroprenyl diene and a chalcone dienophile (Scheme 1) [8]. The diene is usually derived from a flavonoid, such as flavone, flavanone, flavonol, flavanonol, or from a monoterpene, such as myrcene and β‐trans‐ocimene. The dienophile of this class of Diels‐Alder compounds is exclusively derived from a chalcone derivative. Subsequent oxidation and cyclization steps of these flavonoid Diels‐Alder adducts can result in more complex structures. The Diels‐Alder adducts bearing the cis‐trans stereochemistry on the cyclohexenyl ring would be derived through an endo transition state (12), whereas the trans‐trans stereochemistry arises from the exo transition state (13) (Scheme 1) [8]. The stereochemistry of these adducts, including the absolute configuration on the cyclohexene ring, has been explicitly confirmed by circular dichroism (CD) spectroscopic evidence [9] and X‐ray crystallographic analysis [10, 11]. The unique structural features and diverse activities of these adducts have recently aroused much interest of synthetic and medicinal chemistry. The main topics addressed in this chapter are biosynthesis and biomimetic synthesis of flavonoid Diels‐Alder natural products and about 40 references are cited. As the flavonoid Diels‐Alder natural products are composed of a diverse family of secondary metabolites, other subclasses where the dienophile is not a chalcone (e.g. mongolicin B, ‐E, sanggenon B, ‐R, ‐S, dimoracin, mulberrofuran H, meroterpene, pauferrol A derivatives, etc) are not covered in this chapter.

Scheme 1.

Stereochemistry on the cyclohexene ring of flavonoid Diels‐Alder natural products.

2. Biosynthesis of the flavonoid Diels‐Alder natural products

Although the biosynthesis of the flavonoid Diels‐Alder natural products that derived from a monoterpene is not well‐studied [12, 35], it is hypothesized that a Diels‐Alder reaction between a chalcone dienophile and a monoterpene (β‐trans‐ocimene or myrcene) would lead to the direct formation of these adducts (Figure 2).

Figure 2.

Plausible biosynthesis of flavonoid Diels‐Alder natural products that derived from a monoterpene.

The biosynthesis of the mulberry Diels‐Alder flavonoids has been intensively studied by Professors Taro Nomura and Shinichi Ueda. The biosynthetic studies of these adducts were carried out in the callus tissues of Morus alba L [13]. In their pioneering studies, the callus tissues induced from the leaves or seedlings were cultivated and subjected to selection over a period of 9 years for cell strains with high‐pigment productivity [14]. Extraction of these high pigmented cell cultures resulted in isolation of six Diels‐Alder adducts, kuwanons J (1), Q (23), R (24), V (25), mulberrofuran E (26), and chalcomoracin (27) along with morachalcone A (28), isobavachalcone (29), and moracin C (30) (Figure 3) [15–18].

Figure 3.

Metabolites isolated from the Morus alba cell cultures [15–18].

The structures of metabolites 1, 23−27 suggested that they are either the Diels‐Alder adducts from a prenylchalcone and a dehydroprenylchalcone or the Diels‐Alder adducts from a prenylchalcone and a dehydroprenyl‐2‐arylbenzofuran. Nomura and co‐workers hypothesized that kuwanon J (1) was an adduct of morachalcone A (28) and dehydroprenylmorachalcone A. Kuwanon Q (23) was an adduct of isobavachalcone (29) and dehydroprenylmorachalcone A. Kuwanon R (24) was an adduct of morachalcone A (28) and dehydroprenylisobavachalcone. Kuwanon V (25) was an adduct of isobavachalcone (29) and dehydroprenylisobavachalcone. Chalcomoracin (27) was an adduct of morachalcone A (28) and dehydroprenylmoracin C. Mulberrofuran E (26) was an adduct of isobavachalcone (29) and dehydroprenylmoracin C. It is interesting that these Diels‐Alder metabolites and their monomeric precursors (morachalcone A, isobavachalcone and moracin C) were isolated from M. alba cell cultures. In addition, the callus tissue can produce 100 times more mulberrofuran E and chalcomoracin than the intact plant [15–17]. The biosynthetic studies of these Diels‐Alder adducts were further examined through feeding experiments of various exogenous substrates and putative precursors to the M. alba cell cultures.

2.1. Feeding experiments with ¹³C‐labeled acetate to the Morus alba cell cultures

Acetate is an important carbon source for biosynthesis studies in M.alba cell cultures. Feeding experiments of [1–¹³C]‐, [2–¹³C]‐, or [1, 2–¹³C₂]‐acetates to the M.alba cell cultures resulted in the highly ¹³C‐enriched aromatic carbons of chalcomoracin (27) and kuwanon J (1), indicating that both 27 and 1 are derived from two molecules of cinnamoylpolyketide precursors (Figure 4) [19]. From the labeling patterns, the chalcone moiety (34) of both chalcomoracin (27) and kuwanon J (1) is hypothesized to be derived via deoxygenation at C‐5 of the cinnamoylpolyketide precursor 31, followed by Claisen condensation and aromatization (Figure 5) [20]. The 2‐arylbenzofuran moiety (36) of 27 and 1 is hypothesized to be derived by the Aldol condensation at C‐3 and C‐8 of the cinnamoylpolyketide precursor 32, followed by decarboxylation and aromatization (Figure 5) [19].

Figure 4.

¹³C‐labeling patterns of Kuwanon J and chalcomoracin from [1‐¹³C]‐, [2‐¹³C]‐, or [1, 2‐¹³C₂]acetate [19].

Figure 5.

Hypothesized conversion of the chalcone and 2‐arylbenzofuran moieties from cinnamoylpolyketide precursor [19].

However, unlike the aromatic carbons, the isoprene units of chalcomoracin were marginally labeled (∼0.4% enrichment) [19]. On the basis of ¹³C–¹³C spin coupling in the ¹³C‐NMR spectrum, the labeling of [2–¹³C] acetate was incorporated into the starter acetate carbons in the biosynthesis of the isoprene unit of chalcomoracin (27). On the contrary, the [1–¹³C] acetate was not incorporated in the isoprene unit of chalcomoracin (27) [19]. These findings suggested that a tricarboxylic acid (TCA) cycle was involved in the biosynthesis of the isoprenyl unit of chalcomoracin [8]. The rational of this hypothesis was derived from the ¹³C‐labeling experiments. In the experiment with [2–¹³C] acetate, the contiguous ¹³C labels can be derived from the methyl groups of the intact acetate administered by way of at least two passages through the TCA cycle [19]. In the experiment with [1–¹³C] acetate, the ¹³C label was not found in the isoprenyl unit, presumably due to the removal of carbon dioxide during passage through the TCA cycle (Figure 6).

Figure 6.

Formation of reorganized [1, 2‐¹³C₂]acetate through the TCA cycle [19].

This hypothesis was reinforced by the feeding experiment with [2–¹³C] acetate in a pulsed manner (three times, every 12 h) to the M. alba cell cultures [21]. The result from this experiment enabled the identification of the satellite peaks based on the ¹³C–¹³C spin coupling between carbons at C‐25’’ and C23’’, C‐7’’ and C‐1’’, C‐23’’ and C‐24’’ as well as C‐6’’ and C‐1’’ of chalcomoracin. The ¹³C‐enrichment at C‐7’’ and C‐25’’ occurred after the first and third [2–¹³C] acetate administrations but not at the second administration suggested the isomerization between the 3,3‐dimethylallyl and 3‐methylbutadienyl groups (Figure 7) [8]. The coupling patterns of the central carbons (C‐1’’ and C‐23’’) appeared as doublet signal instead of the doublet of doublet signal indicated that these central carbons are independently coupled with the adjacent methyl carbons. Nomura et al. hypothesized that the independent ¹³C‐labeling pattern at the isoprenyl unit might due to the transfer of ¹³C‐labeling from cis‐methyl to trans‐methyl through the diene formation (Figure 7) [8, 21]. Taken together, these findings gave conclusive evidence on the diene formation from the isoprenyl moiety for the Diels‐Alder cycloaddition reaction. Thus, the feeding experiment with ¹³C‐labeled acetate revealed that the Diels‐Alder adducts chalcomoracin and kuwanon J are biosynthesized through the [4 + 2] cycloaddition reaction between two cinnamoylpolyketide‐derived molecules [8].

Figure 7.

Two independent ¹³C‐labeling patterns at the isoprenyl units of chalcomoracin and the transfer of the ¹³C‐labeling from cis‐methyl carbon to trans‐methyl carbon through the diene formation [8, 19].

2.2. Feeding experiments with methoxychalcone and prenylated flavone precursors

Based on the fact that methoxychalcone or methoxy‐substituted Diels‐Alder adducts have not been found in the M. alba cell cultures, therefore involvement of these precursors in the construction of the Diels‐Alder adducts would be an important evidence for the enzymatic intermolecular Diels‐Alder reaction in M. alba cell cultures.

Indeed, feeding methoxychalcone 37 to the cell cultures yielded prenylchalcone 38 and Diels‐Alder adducts 40−43 (Figure 8) [22]. The formation of the prenylchalcone 38 from methoxychalcone 37 in the cell cultures indicated that isoprenylation occurs after the formation of chalcone skeleton from cinnamoylpolyketide precursor.

Figure 8.

Feeding experiments of methoxychalcone derivatives to the M. alba cell cultures [22].

The metabolites 40−43 revealed that the methoxychalcone 37 was incorporated into the Diels‐Alder adducts. Interestingly, when the synthetic prenylchalcone 38 was fed to the cell cultures, the same Diels‐Alder metabolites 40−43 were isolated. Similarly, the feeding experiment of trimethoxychalcone 39 afforded the Diels‐Alder metabolite 44 [22]. Taken together, these results suggested that both the requisite diene and dienophile can be derived from the same chalcone precursor. For example, dehydrogenation of the prenyl unit of chalcone 38, followed by intermolecular [4 + 2] cycloaddition reaction with the α, β‐double bond of another chalcone 38 leads to the formation of the Diels‐Alder adduct 42 (Figure 8).

In addition, all these Diels‐Alder metabolites derived from the methoxychalcone precursors were optically active and have the same stereochemistry as that of chalcomoracin (27) and kuwanon J (1). The results based on the feeding experiments of methoxychalcone derivatives revealed that the [4 + 2] cycloaddition reaction in the M. alba cell cultures is an enzymatic process.

Nomura et al. further attempted the synthesis of Diels‐Alder natural product, artonin I (46) by using M. alba cell cultures (Figure 9) [23]. Although it is theoretically possible that artonin I could be derived from a chalcone dienophile (morachalcone A 28) and a prenylflavone diene (45), but precursor of 45 (artocarpesin 47) has not been found in M. alba cell cultures. Indeed, feeding 47 to the M. alba cell cultures resulted in the isolation of artonin I (46) through dehydrogenation of the prenyl group of 47 followed by the enzymatic [4 + 2] cycloaddition reaction with an endogenously generated morachalcone A 28. This is the first example of a natural product’s structure elucidation through enzymatic synthesis by using M. alba cell cultures [8].

Figure 9.

Biosynthesis of artonin I by administration of artocarpesin to the M. alba cell cultures [23].

3. Biomimetic synthesis of the flavonoid Diels‐Alder natural products

The Diels‐Alder cycloaddition reaction which named after Otto Paul Hermann (1876–1954) and Kurt Alder (1902–1958) was discovered during their studies on the reaction of benzoquinone and cyclopentadiene in 1928. Today, this cycloaddition reaction is a well‐known method that is widely used to synthesize a six‐membered cyclic compound in a regio‐ and stereocontrolled way. The following section discusses the use of this powerful synthetic methodology to prepare flavonoid Diels‐Alder natural products based on the biosynthesis models.

3.1. Thermal conditions

During the early studies of the Diels‐Alder cycloaddition reaction, the reaction was essentially carried out under thermal conditions owing to the simplicity of the experimental setup and the efficiency of the thermal process. Today, thermal promoted Diels‐Alder cycloaddition reaction remains the first line approach for the construction of a six‐membered cyclic compound, including that of flavonoid Diels‐Alder natural products [24–30].

In 2010, Rizzacasa and co‐workers reported the synthesis of racemic methyl ether derivatives of chalcomoracin, mongolicin F, mulberrofurans C and J via thermal Diels‐Alder reaction (180°C in toluene) between chalcone dienophiles (39 and 49) and a dehydroprenyl‐2‐arylbenzofuran diene (48) (Scheme 2). The thermal Diels‐Alder reaction resulted in a mixture of endo‐ and exo‐diastereomers in almost equal quantity [24].

Scheme 2.

Synthesis of (±)‐mulberrofuran J (50), (±)‐mulberrofuran C (51), (±)‐mongolicin F (52), and (±)‐chalcomoracin (53) hexamethyl ethers by thermal Diels‐Alder reaction [24].

Rizzacasa and co‐workers also reported a similar strategy for the synthesis of (±)‐kuwanon I and J hexamethyl ethers. They hypothesized that the presence of an ortho‐phenol group in the chalcone dienophile was essential for the Diels‐Alder cycloaddition reaction. However, attempts to deprotect the methyl ethers of these Diels‐Alder adducts using various demethylating agents were unsuccessful [25].

Rahman and co‐workers utilized the thermal‐promoted Diels‐Alder reaction to synthesize (±)‐dorsterone, (±)‐kuwanon V and (±)‐morusalbanol A pentamethyl ethers based on the biosynthesis models [27, 29, 30].

3.2. High pressure conditions

Although the thermal‐promoted Diels‐Alder reaction provides a rapid entry to flavonoid Diels‐Alder adducts, this method may not be successful due to the instability of the diene or dienophile under a high‐temperature condition. This limitation can be overcame using a high‐pressure system for the Diels‐Alder reaction.

In 2013, Mcleod and co‐workers utilized this strategy to synthesize (±)‐panduratin A (4) and (±)‐4‐hydroxypanduratin A (58) [31]. Instead of late‐stage Diels‐Alder cycloaddition to synthesize the cyclohexenyl core of 4 and 58, they initiated the biomimetic Diels‐Alder reaction in an early stage by using methyl cinnamate (54) and β‐trans‐ocimene (20) (Scheme 3). High‐pressure Diels‐Alder reaction between 54 and 20 in dichloromethane at 19 kbar at room temperature gave a mixture of (±)‐panduratin I (56) and (±)‐panduratin H (57) in 1:2.9 ratio in 93% yield after 3 days. Subsequent transformations of panduratin H 57 afforded the natural products (±)‐panduratin A and (±)‐4‐hydroxypanduratin A in three more further steps.

Scheme 3.

Biomimetic synthesis of (±)‐panduratin A and (±)‐4‐hydroxypanduratin A by using high pressure conditions [31].

3.3. Single electron transfer initiated Diels‐Alder reaction

In 1960 when Yates and Eaton first reported the acceleration of the Diels‐Alder reaction by Lewis acid catalysts, a variety of Lewis acid catalysts have been developed to accelerate the reaction [32].

Porco and co‐workers developed a Lewis acid catalyst system that composed of multiple components (CoI₂/o‐phenanthroline/ZnI₂/Bu₄NBH₄) for the [4 + 2]‐cycloaddition reaction between 2′‐hydroxychalcone dienophiles and various simple dienes [33]. They hypothesized that the mechanism of this catalytic system was a single electron transfer initiated process (Scheme 4).

Scheme 4.

Proposed mechanism for an electron transfer‐initiated Diels‐Alder cycloaddition reaction [33].

According to their report, the role of CoI₂and Bu₄NBH₄was hypothesized to be an electron donor [33]. As outlined in Scheme 4, coordination of ZnI₂ activated the carbonyl of 2′‐hydroxychalcone 59 to form complex 62. In the presence of electron donors, complex 62 may undergo metal‐ion‐promoted single electron transfer to generate a chalcone radical anion 63. The regioselective addition of 63 to the diene should generate a stabilized, allylic radical 64 which may undergo ring‐closing cyclization to produce ketyl intermediate 65. Loss of ZnI₂ from 65 and subsequent single electron transfer to another complex 62 may afford cycloadduct 61, thereby restarting the catalytic cycle [33]. Following this mechanistic studies, Porco et al. further established the total synthesis of (±)‐nicolaioidesin C (9) by using myrcene as a diene (Scheme 5) [33].

Scheme 5.

Biomimetic synthesis of (±)‐nicolaioidesin C (9) [33].

Rahman and co‐workers used the thermal‐promoted as well as single‐electron‐transfer‐initiated Diels‐Alder reaction to compare the efficiency of the biomimetic synthesis of (±)‐kuwanon V (71) and (±)‐doresterone (70) methyl ethers [27]. Thermal Diels‐Alder cycloaddition between dienophile 69 and diene 68 in a pressure tube at 160°C for 18 h afforded 70 (exo‐adduct) and 71 (endo‐adduct) in 55% yield in a 1.5:1 ratio (Scheme 6). A comparable result (48% yield, 1.7:1 ratio) was obtained by using the single electron transfer initiated Diels‐Alder reaction (ZnI₂, Bu₄NBH₄, CoI₂, 1, 10‐phenanthroline in 60:10:10:10 mol%).

Scheme 6.

Biomimetic synthesis of (±)‐dorsterone and (±)‐kuwanon V pentamethyl ethers [27].

Recently, Valentina et al. reported the synthesis of (±)‐kuwanol E and the heptamethyl ether derivative of (±)‐kuwanol Y by using a combination of thermal conditions and Lewis acid catalyst [34]. The key synthetic step involved a borane tetrahydrofuran mediated biomimetic intermolecular Diels‐Alder cycloaddition reaction. It is noteworthy that the endo/exo diastereoselectivity of the reaction was proven to be temperature‐controlled.

3.4. Chiral ligand‐Brønsted acid catalysis

The first asymmetric synthesis of flavonoid Diels‐Alder natural products was reported by Palomo and co‐workers in 2010 (Scheme 7). They employed a recoverable chiral auxiliary ((1 R)‐(+)‐camphor) in the asymmetric synthesis of nicolaioidesin C (9) [35]. First, the biomimetic Diels‐Alder reaction between myrcene 18 and α′‐hydroxy enone dienophile 72 was catalyzed by triflic acid at ‐78°C in dichloromethane to afford an enantiomeric enriched intermediate 73 in 85% yield. Subsequent transformation of the intermediate 73 in five further steps afforded (‐)‐nicolaioidesin C (9).

Scheme 7.

Asymmetric biomimetic synthesis of (‐)‐nicolaioidesin C (9) [35].

3.5. Silver nanoparticles catalyzed dehydrogenative Diels‐Alder reaction

In 2010, Porco and co‐workers discovered that silver (0) nanoparticles (AgNp) could effectively catalyze the Diels‐Alder cycloaddition reaction [36]. The AgNP was prepared from a 3:1 molar ratio of AgBF₄/Bu₄NBH₄ in CH₂Cl₂ and then coated with silica gel. The solid product was filtered and then calcinated at 220°C to give AgNP. A proposed catalytic cycle was showed in Scheme 8 [36]. It was hypothesized that proton removal and single electron transfer from the absorbed chalcone 59 to the silver nanoparticles may generate the AgNP‐stabilized phenoxyl radical intermediate 74 which is in resonance with the radical 75. A proposed concerted Diels‐Alder reaction between the radical intermediate 74/75 and diene 60 provides 76 which generates 55 via back electron transfer (BET) and protonation [36]. A final desorption step gave the Diels‐Alder adduct 61. Porco and co‐workers hypothesized that this silver nanoparticle (AgNp) may serve as ‘electron shuttle’ catalysts by accepting and returning a single electron from and to the substrate [36].

Scheme 8.

Proposed mechanism for the silver nanoparticles‐catalyzed Diels‐Alder reaction [36].

Following the mechanistic studies, Porco et al. utilized AgNP for the biomimetic syntheses of (±)‐panduratin A (Scheme 9) [36] and (±)‐sorocenol B (Scheme 10) [37]. Inspired by the aforementioned biosynthesis studies, Porco and co‐workers found that the AgNP can also be used to promote dehydrogenation of the prenyl group of a flavonoid to form the requisite diene for the Diels‐Alder reaction with a 2’‐hydroxychalcone dienophile. Such tandem reactions were successfully employed for the synthesis of (±)‐brosimone A and (±)‐brosimone B (Scheme 11) [38].

Scheme 9.

Synthesis of (±)‐panduratin A (4) [36].

Scheme 10.

Biomimetic synthesis of (±)‐sorocenol B [37].

Scheme 11.

Biomimetic synthesis of (±)‐brosimone A and (±)‐brosimone B [38].

3.6. Chiral ligand‐Lewis acid complex mediated Diels‐Alder reaction

In 2014, Lei and Wulff et al. reported the first enantioselective total synthesis of (‐)‐kuwanon I (2), (+)‐kuwanon J (1), (‐)‐brosimone A (86) and (‐)‐brosimone B (84) by using chiral ligand‐Lewis acid complex. This complex was prepared by coordination of an axially chiral ligand such as VANOL or VAPOL to borane [39].

Scheme 12 shows the mechanism proposed by Lei and co‐workers for the enantioselective Diels‐Alder reaction [39]. The mechanism was proposed to proceed through the formation of a chiral boron complex 88, followed by formation of a tetracoordinate boron complex 89 with 2′‐hydroxychalcone dienophile. Subsequently, Diels‐Alder reaction between the chiral complex 89 and a diene afforded a mixture of endo/exo diastereomers in high enantiomeric excess. Lei and co‐workers proposed that the enantioselective Diels‐Alder reaction may be induced by the following factors [39, 40].

Scheme 12.

Proposed mechanism for the chiral ligand‐Lewis acid complex mediated enantioselective Diels‐Alder reaction [39, 40].

1. The coordination bond between boron and dienophile which may lower the energy of LUMO.

2. The mobility of dienophile may be reduced upon complexation.

3. The π‐π stacking between the chiral ligand and dienophile shielding one face of the chalcone dienophile from attack by the diene.

Following the mechanistic studies, the (S)‐VANOL‐borane complex was efficiently used to mediate the synthesis of (‐)‐kuwanon I (2), (+)‐kuwanon J (1), (‐)‐brosimone A (84) and (‐)‐brosimone B (85) [39]. Asymmetric Diels Alder reaction for these molecules was summarized in Schemes 13–15.

Scheme 13.

Chiral ligand‐Lewis acid complex mediated enantioselective synthesis of (–)‐kuwanon I (2) and (+)‐kuwanon J (1) [39].

Scheme 14.

Enantioselective synthesis of (–)‐brosimone B [39].

Scheme 15.

Enantioselective synthesis of (–)‐brosimone A [39].

Based on the reported results, the chiral ligand strongly influences the enantioselectivity of the cycloaddition reaction. A 2.5 equivalent of (R)‐VANOL is required for the optimal formation of kuwanon J precursor endo‐95 (97% ee, 1.1:1 endo/exo), whereas similar amount of (S)‐8, 8’‐dimethyl‐VANOL is required for the optimal formation of kuwanon I precursor exo‐94 (84% ee, 1.2:1 exo/endo). Finall, deprotection of the acetate group of endo‐95 and exo‐94 furnished the desired natural products (-)‐kuwanon J (1) and (+)‐kuwanon I (2), respectively (Scheme 13) [39].

The synthetic routes for (–)‐brosimone B (84) and (–)‐brosimone A (86) were showed in Schemes 14 and 15, respectively. For (–)‐brosimone B (84), cycloaddition reaction between dienophile 97 and diene 98 using (S)‐VANOL gave a mixture of diastereomers 99 and 100 in 71% yield in a 1.2:1 ratio. Remarkably, excellent enantiomeric excess (ee) values for both compounds were obtained (98% ee for 100, 93% ee for 99). Deprotection of the acetyl groups of 100 gave (-)‐brosimone B in 70% yield (Scheme 14) [39, 40].

The diene 98 was also used in the synthesis of brosimone A (86) in a one‐pot inter‐/intramolecular Diels‐Alder cycloaddition cascade strategy (Scheme 15). The (S)‐VANOL‐borane complex efficiently mediated the cycloaddition reaction to give a mixture of three diastereomers 101−103 (Scheme 15). Deprotection of the adduct 103 gave (-)-brosimone A (86) in 70% yield [39, 40].

In 2016, Porco and co‐workers reported the syntheses of the flavonoid Diels‐Alder natural products sanggenon C (108) and sanggenon O (109) by using a combination of silver nanoparticles (AgNP) and a BINOL‐borate catalyst (Scheme 16) [41].

Scheme 16.

Asymmetric synthesis of sanggenons C (108) and O (109) [41].

A catalytic amount of triphenylborate (B(OPh)₃) and (R)‐3,3′‐dibromoBINOL was used to mediate the asymmetric Diels‐Alder reaction between diene precursor 104 and dienophile 105 (Scheme 16). In the first step, the diene precursor 104 underwent a retro 6π‐electrocyclisation followed by a formal 1,7 hydrogen shift process to afford the requisite diene functionality. Reaction of this diene with dienophile 105 in the present of a catalytic amount of chiral BINOL‐borate complex ((S)‐3,3′‐dibromoBINOL/triphenylborate) afforded a mixture of cycloadducts, which after deprotection gave sanggenon C (108) and sanggenon O (109) in 2:1 ratio of 98 and 93% ee, respectively. The use of AgNP gave a racemic mixture of 108 and 109.

In conclusion, this chapter has provided an overview of biosynthesis and biomimetic synthesis of flavonoid Diels‐Alder natural products. Intensive biosynthesis studies led by Nomura et al. have provided important information for the enzymatic formation of these natural products. In particular, information from the diene formation and the feeding experiments have paved the way for an exploration of chemical synthesis of these natural products. Finally, with the innovative chemical strategies, enantiomerically pure flavonoid Diels‐Alder natural products were made possible for further biological activities evaluation.