2
Oxepin Natural Products
Racemic senoxepin (11), a norsesquiternelactone found in Senecio platyphylloides, was the first oxepin-containing natural product obtained by total synthesis by Bohlmann in 1989 (Scheme [2]).[5] Starting from methyl 3,5-hexadienoate (7), epoxide 8 was synthesized in 14 steps. Allylic bromination of 8 with azobisisobutyronitrile (AIBN) and N-bromosuccinimide (NBS) produced the dibromide 9, which was directly subjected to Finkelstein conditions resulting in diene 10. Spontaneous disrotatory electrocyclic rearrangement to the oxepin followed by Peterson olefination provided senoxepin (11). Initial attempts to install the exo-methylene group via Oshima methylenation (CH2Br2/Zn/TiCl4) resulted in degradation of the oxepin to give a benzene core.
Scheme 2 Arene oxide rearrangement for the construction of the oxepin motif in senoxepin 11 by Bohlmann
In 2012, Taylor reported the total synthesis of janoxepin (19), a leucine-derived oxepin-pyrimidinone-ketopiperazine natural product (Scheme [3]).[6] Janoxepin (19) was isolated from the fungus Aspergillus janus and possesses antiplasmodial effects against the malaria parasite Plasmodium falciparum 3D7 strain. Diene 13 was generated in seven steps using leucine (12) as the starting material. Upon exposure to Grubbs second-generation catalyst, dihydrooxepin 14 was obtained in 81% yield. A two-step condensation procedure under basic conditions provided the desired isopropyl group in 15. Nevertheless, during these steps, isomerization occurred with loss of stereoinformation. Riley oxidation afforded the desired alcohol 17 in 50% yield as an equimolar mixture of diastereomers together with the ketone 16 (10%). The latter was converted back into the alcohol 17 with sodium borohydride. While elimination proved challenging under various standard conditions, the alcohol 17 was transformed into the chloride using mesyl chloride. Tetrabutylammonium fluoride (TBAF) mediated dehydrohalogenation gave the desired oxepin 18 in low yield (10%) together with a mixture of unidentified byproducts. Final hydrolysis of the imidate functionality afforded janoxepin (19).
Scheme 3 Ring-closing metathesis for the construction of the oxepin motif in janoxepin (19) by Taylor
A more frequent structural motif in nature is benzoxepin, which does not undergo the previously described isomerization to the corresponding arene oxides. The benzoxepin salvianolic acid N (25) was isolated from Danshen, the dried root and rhizome of Salvia miltiorrhiza Bunge (Scheme [4]).[7] Danshen is a traditional Chinese drug used for the treatment of coronary artery disease and is known to possess antiviral, antioxidant, and antitumor activities. The reported total synthesis began with aldehyde 20, which was converted into bromide 21 via bromination and tosylation. Protection of the phenol as its tosylate proved to be essential to obtain the required Z-selectivity with ylide 22 (ratio 5:1) for stilbene formation. Intramolecular Ullmann coupling under optimized conditions (copper(I)triflate, caesium carbonate) afforded oxepin 24 in 88% yield. Completion of the synthesis of salvianolic acid N (25) was achieved in a further seven steps.
Scheme 4 Ullmann coupling for the construction of the oxepin motif in salvianolic acid N (25) by Zhang
Scheme 5 Ullmann coupling for the construction of the oxepin motif in secosarcocapnine (30) by Castedo
In 1991, Castedo reported the synthesis of norsecosarcocapnine (29), which also gave access to secosarcocapnine (30) via an intramolecular Ullmann coupling (Scheme [5]).[8] Subsequent Cope elimination of the piperidine motif gave the desired oxepin structure. Reduction of the hydroxylamine moiety with zinc and sulfuric acid gave norsecosarcocapnine (29), which was then methylated with either methyl iodide followed by treatment with sodium ethanolate or by reductive amination using formaldehyde and sodium borohydride to give secosarcocapnine (30).
Exposure of phenol 32, itself derived from dihydroisoquinoline 31 in three steps, to the same Ullmann coupling conditions gave an undetermined diastereomeric mixture of dihydrooxepin 33 (Scheme [6]).[9] Subsequent oxidation using 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) afforded the natural product yagonine (34).
Exposure of 34 to barium hydroxide induced the formation of dihydrooxepin 36 (56%) and aristoyagonine (37) (7%) via benzilic-acid type ring-contraction. Oxidation of the undesired dihydrooxepin 36 with DDQ provided aristoyagonine (37) in excellent yield (Scheme [6]).[9]
Scheme 6 Ullmann coupling for the construction of the oxepin motif in aristoyagonine (37) by Castedo
The first total synthesis of aristoyagonine (37) was reported by Domínguez in 1995 (Scheme [7]).[10] The first part of the synthesis involved the conversion of thioacetal 38 into phenol 39. Again, an Ullmann coupling was applied to produce the dihydrooxepin 40. The presence of the thioacetal group turned out to be beneficial as other functionalities caused significant formation of side products. Finally, the lactam of aristoyagonin (37) was assembled in eight further steps.
Scheme 7 Ullmann coupling for the construction of the oxepin motif in aristoyagonine (37) by Domínguez
An additional total synthesis of aristoyagonine (37) was accomplished by Grandclaudon in 2004 and allowed shortening of the route to five steps (Scheme [8]).[11]
Scheme 8 Ullmann coupling for the construction of the oxepin motif in aristoyagonine (37) by Grandclaudon
Carboxylic acid 41 was converted into phosphorylated-isoindolinone 42 in two steps. Wittig type reaction employing lithium bis(trimethylsilyl)amide (LHMDS) and 18-crown-6 yielded alkene 45. During demethylation with boron trichloride, full isomerization of the alkene was observed, yielding only the Z-isomer, which was directly annulated under Ullmann coupling conditions to give aristoyagonine (37).
In 2013, aristoyagonine (37) was synthesized by Ho in five steps from aldehyde 20 (Scheme [9]).[12] The one-pot cascade reaction of isoindoline 46 directly afforded the dibenzoxepin lactam aristoyagonine (37) via a one-pot sequence in 68% yield.
Scheme 9 Ullmann coupling for the construction of the oxepin motif in aristoyagonine (37) by Ho
Scheme 10 Wittig type reaction for the construction of the oxepin motif in pacharin (52) by Sargent
While intramolecular Ullmann coupling was shown to be an attractive and powerful method for the synthesis of seven-membered oxacycles, Sargent reported the synthesis of pacharin (52) via an intermolecular Ullmann coupling (Scheme [10]).[13] An eight-step sequence gave access to diaryl ether 49. Treatment of 49 with triphenylphosphine generated bisylide 50. Upon exposure of 50 to oxygen, the desired oxepin 51 was formed. A final deprotection step using boron trichloride allowed for selective removal of the isopropyl groups to afford pacharin (52).
3
Dihydrooxepin Products
In contrast to oxepin, the dihydrooxepin structure is more frequently found in natural products. Due to the different possibilities for the arrangement of the double bonds, there are significantly more options available for the construction of these heterocycles. In the following, we have ordered the syntheses according to the different strategies employed to build up the seven-membered ring system.
Scheme 11 Acid catalyst acetalization for the construction of the dihydrooxepin motif in (+)-cladoacetal A (55) and (–)-cladoacetal B (57) by Lin
3.1
Brønsted or Lewis Acid Catalyzed Cyclization
Cladoacetal A (55) and B (57) were isolated from solid-substrate fermentation cultures of an unidentified fungicolous isolate (NRRL 29097) resembling Cladosporium species. So far, only cladoacetal A (55) demonstrated antibacterial activity. While the relative configurations were determined by NMR spectroscopy shortly after the isolation, the absolute configurations were only determined by the first total synthesis by Lin in 2012. Enantioselective syntheses of cladoacetal A (overall yield: 16%) and B (overall yield: 34%) proceeded in nine and seven steps, respectively, employing crotonaldehyde (53) as the starting material (Scheme [11]).[14] The dihydrooxepin core of both natural products was synthesized from bisoxolane 54 and 56 via intramolecular acetalization promoted under thermal (70 °C) acidic conditions (p-TSA). Final methyl deprotection with freshly prepared sodium ethanethiolate afforded (+)-cladoacetal A (55) in 76% and (–)-cladoacetal B (57) in 90% yield over two steps, respectively.
In 2018, She published a bioinspired total synthesis of the natural product (–)-gymnothelignan L (62), which was isolated from Gymnotheca chinensis Decne, a widely used perennial Chinese herb (Scheme [12]).[15] Structurally, 62 is classified as a dibenzocyclooctene-type lignin natural product in which the chiral axial biphenyl scaffold is fused to the THF ring, to form a bridged dihydrooxepin backbone.
Scheme 12 Lewis acid mediated Friedel–Crafts alkylation for the construction of the dihydrooxepin motif in (–)-gymnothelignan L (62) by She
The aldehyde 58 served as the starting point of the synthesis and was converted into lactone 59 in twelve steps. The adjacent stereocenters of the lactone were introduced by an asymmetric Evans aldol reaction and the second methyl group by α-methylation of the corresponding lactone. With enantiomerically pure material in hand, the [4.2.1]-bicyclic ether core was constructed via an intramolecular transannular Friedel–Crafts reaction. Diisobutylaluminium hydride (DIBAL-H) mediated reduction of the γ-butyrolactone 59 afforded the corresponding lactol. Subsequent treatment with boron trifluoride–diethyl etherate at –78 °C generated oxocarbenium cation 60, which underwent the Friedel–Crafts cyclization upon slow warming of the reaction mixture to –30 °C to give dihydrooxepin 61 in 68% yield over two steps. Finally, reductive cleavage of the benzyl group with a catalytic amount of palladium on charcoal furnished the natural product (–)-gymnothelignan L (62).
Similar to the already described synthesis of (–)-gymnothelignan L (62), a route to (–)-gymnothelignan V (67) was published by Reutrakul in the same year under slightly modified conditions (Scheme [13]).[16] Starting from enantiopure lactone 63, four further steps yielded the natural product gymnothelignan J (64) as a mixture of two diastereomers (d.r. = 4:1). Upon treatment of 64 with a catalytic amount of p-TSA, both diastereomers generated the same oxocarbenium cation 65, which readily underwent stereoselective intramolecular Friedel–Crafts cyclization to afford (–)-gymnothelignan V (67) together with its epi-isomer (68) as an inseparable mixture (90%, d.r. = 9:1). The formation of 68 was proposed to proceed through the lactol ring-opening under acidic conditions followed by epimerization of the α-methyl group of aldehyde 66. Separation of the diastereomers was accomplished by using the TBS-protected phenol derivative of 64, which after desilylation gave pure (–)-gymnothelignan V (67).
Scheme 13 Friedel–Crafts alkylation for the construction of the dihydrooxepin motif in (–)-gymnothelignan V (67) by Reutrakul
3.2
Radical Cyclisation
In recent years, numerous tricyclic dibenzo[b,f]oxepin natural products such as bauhinoxepin J (71) were isolated from plants belonging to the Bauhinia genus, in particularly Bauhinia purpurea. After its isolation in 2007, 71 was found to exhibit remarkable biological activities including antimycobacterial, antimalarial, and tumor growth inhibitory activity, making bauhinoxepin J (71) an interesting target for synthesis. The first total synthesis was accomplished by Kraus in 2009 (Scheme [14]).[17] The synthesis began with chromanone 69, which was converted into carboxylic acid 70 in three steps. The key radical intramolecular cyclisation step was based on work of DeKimpe and was promoted by the addition of ammonium persulfate to 70. This gave bauhinoxepin J (71) in 40% isolated yield and an overall yield of 22% over four steps.
Scheme 14 Radical cyclization for the construction of the dihydrooxepin motif in bauhinoxepin J (71) by Kraus
3.3
Substitution and Addition Cyclization
A second route to bauhinoxepin J (71) was published by Katoh. Starting from trioxybenzene 72 the synthesis proceeded in 33% yield over six steps (Scheme [15]).[18] The final cyclization of the seven-membered dihydrooxepin ring was accomplished under mild basic conditions and involved intramolecular nucleophilic 1,4-addition of phenol 73 and subsequent elimination to give bauhinoxepin J (71).
Scheme 15 1,4-Addition/elimination for the construction of the dihydrooxepin motif in bauhinoxepin J (71) by Katoh
A further member of this natural product family, bauhinoxepin C (79), was synthesized via a one-pot sequence developed by Ngernmeesri in 2021 (Scheme [16]).[19] 2-Methylresorcinol (74) was converted into aldehyde 75 in three steps. Under optimized conditions, oxepin 77 was synthesized in 49% yield, by reaction with nitro-phenol 76 under basic conditions. In the proposed reaction mechanism biaryl ether formation occurred via an intermolecular nucleophilic aromatic substitution reaction. A subsequent intramolecular Knoevenagel reaction afforded the oxepin substructure. Upon exposure of 77 to palladium on charcoal under an atmosphere of hydrogen gas, reduction of the nitro group and the C10–11 double bond occurred. The obtained aniline was directly used in a diazotization–substitution sequence to produce phenol 78 in 45% yield over two steps. Regioselective demethylation with boron tribromide was proposed to occur via coordination of the oxygen in the seven-membered ring to yield bauhinoxepin C (79) in 47% yield.
Scheme 16 Nucleophilic aromatic substitution and Claisen condensation cascade for the construction of the oxepin motif in bauhinoxepin C (79) by Ngernmeesri
The synthesis of benzyltetrahydroisoquinoline based natural product cularine (82) was reported by Lumb in 2021. The first enantioselective synthesis of (S)‑cularine (82) was accomplished by initially using aldehyde 20 as the starting material.[20] The utilization of Ellman’s chiral sulfonamide and modification of the Pomeranz–Fritsch cyclization held promise to generate the C4-C4a bond and reveal the isoquinoline. Within twelve further steps, phenol 80 was accessible. The use of a 4-nitrophenyl leaving group was required for the substitution reaction of the o-quinone generated in situ. Simple removal of the silyl protecting group with TBAF in the presence of air induced o-quinone formation and intramolecular substitution. The instable product was treated with methyl iodide to yield dihydrooxepin 81 in 62% yield over two steps. Deprotection of the tosyl group (lithium naphthalenide) and reductive methylation (formaldehyde and sodium borohydride) completed the total synthesis of (S)‑cularine (82) (Scheme [17]).
Scheme 17 Redox-neutral substitution for the construction of the dihydrooxepin motif in (S)‑cularine (82) by Lumb
Scheme 18 Friedel–Crafts cyclization for the construction of the dihydrooxepin motif in (±)-cularicine (87) by Maclean
(±)-Cularicine (87) an alkaloid of Corydalis claviculata (L.) DC, was isolated by Manske in 1940. Starting with phenol 83, Maclean published a racemic synthesis of cularicine (87), as shown in Scheme [18].[21] Attempts to cyclize 84 under various acidic conditions turned out to be unsuccessful. Cyclization under Friedel–Crafts conditions with the corresponding acid chloride were reported to give complex product mixtures arising from debenzylation of the ether by the Lewis acid. However, when the acid chloride was converted into amide 85, cyclization to the enamine was observed upon treatment with phosphoryl chloride. After hydrolysis, ketone 86 was obtained. The final four steps of the synthesis were required to build up the piperidine ring system.
In 2000, Yamaguchi reported the synthesis of 2,5-dihydro-1-benzoxepins employing a Mitsunobu cyclization as the key step (Scheme [19]).[22] This strategy was applied to the total synthesis of the radulanins, a family of bicyclic benzoxepins. Starting from readily available 1,3-dimethoxy-5-(2-phenylethyl)benzene 88, triol 89 was accessible via eight steps. Exposure of 89 to standard Mitsunobu conditions (DEAD, PPh3) allowed for efficient ring-closure to furnish radulanin A (90).
Scheme 19 Mitsunobu reaction for the construction of the dihydrooxepin motif in radulanin A (90) and radulanin E (91) by Yamaguchi
The developed strategy was later further expanded to the synthesis of radulanin E (91) via a three-step sequence (temporary protection, Vilsmeier formulation and selective oxidation).[23]
3.4
Sigmatropic Rearrangement
In 2019, Nay published a one-pot synthesis of 2,5-dihydrooxepines through retro-Claisen rearrangements and applied this strategy to the synthesis of radulanin A (90) (Scheme [20]).[24] Theoretical studies were performed to explain the experimental results and the difference in reactivity observed between substrates derived from cyclic or linear 1,3-diketones. Reaction of diketone 92 with 1,4-dibromo-2-methyl-2-butene (93) under basic conditions afforded 94, which underwent retro-Claisen rearrangement to afford dihydrooxepin 95. Subsequent dihydroxylation under standard conditions (NMO, K2OsO4) allowed preparation of diol 96. To complete the synthesis, diol 96 was treated with mesyl anhydride. TBAF promoted elimination of both mesylates and isomerization provided radulanin A (90).
Scheme 20 Retro-Claisen rearrangement for the construction of the dihydrooxepin motif in radulanin A (90) by Nay
Scheme 21 Oxidative cyclization for the construction of the dihydrooxepin motif in (±)-oxyisocyclointegrin (99) by Hawkins
3.5
Oxidative Methods
The oxidation of cyclohexanone derivatives via the Baeyer–Villiger rearrangement is a powerful method for the synthesis of simple seven-membered ring systems. The oxidation of linear alkenes or similar functionalities was also reported as a valuable strategy to access these systems. An example for the use of a linear precursor is the synthesis of oxyisocyclointegrin (99) from integrin (98) (Scheme [21]).[25] To date, it is still unclear if oxyisocyclointegrin (99) exists as a racemate or a single enantiomer as no optical data nor any biological activity of either 98 or 99 were reported during their isolation. The total synthesis of both natural products was disclosed in 2019 by Hawkins starting from ketone 97. Nine steps were required to accomplish the synthesis of integrin (98), which, upon irradiation in the presence of oxygen with a high-pressure mercury lamp, provided oxyisocyclointegrin (99) and its hydroperoxide. The crude residue was then treated with sodium borohydride in methanol to give racemic oxyisocyclointegrin (99) in 84% yield. Biological evaluation of 99 revealed moderate to weak activity against Staphylococcus aureus and prostate cancer cells.
Scheme 22 Bayer–Villiger oxidation for the construction of the dihydrooxepin motif in (–)-acetylaranotin (104) and (+)-MPC1001B (105) by Tokuyama
Owing to their unique structural and biological properties, epidithiodiketopiperazines represent an important class of natural products. Among them, acetylaranotin (104) features a dihydrooxepin moiety fused to a pyrrolidine epidithiodiketopiperazine, which renders it a challenging target for synthetic chemists. In 2012, Tokuyama reported the total synthesis of (–)-acetylaranotin (104) featuring a regioselective Baeyer–Villiger oxidation to efficiently form the proline-fused dihydrooxepin ring (Scheme [22]).[26] The synthesis of enone 101 began with l-Cbz-tyrosine (100). Further screening of a variety of oxidation conditions revealed a combination of trifluoroacetic anhydride (TFAA) and urea hydrogen peroxide (UHP) as the combination of choice. This gave enol lactone 102 as a single isomer in 53% yield. After conversion into an enol triflate, subjection to palladium-catalyzed reduction conditions gave dihydrooxepin 103 in excellent yield with the Cbz group still intact. Nine further steps, including dimerization of the monomer units, were required to finish the synthesis of (–)-acetylaranotin (104).
Four years later, Tokuyama used the same strategy to complete the total synthesis of (+)-MPC1001B (105). The greatest challenges in the synthesis of MPC1001B (105) were the diastereoselective assembly of the characteristic 15-membered ring as well as the labile aldol substructure of the dithiodiketopiperazine.[27]
In 2020, with dihydrooxepin 103 already in hand, Tokuyama reported the total syntheses of (–)-emestrin H (106) and (–)-asteroxepin (107) (Scheme [23]).[28] A major breakthrough during this synthesis was the discovery of the allyloxymethyl (Allom) group as a protecting group for the amide nitrogen of the diketopiperazine core. Most importantly, this group was fully stable under Nicolaou’s sulfenylation conditions and cleavable under mild conditions (tetrakis(triphenylphosphin)palladium (Pd(PPh3)4) and N,N-dimethylbarbituric acid) without affecting the acid-sensitive dihydrooxepin structure.
Scheme 23 Synthesis of (–)-emestrin H (106) and (–)-asteroxepin (107) from dihydrooxepin 103 by Tokuyama.
In 2017, Isaka reported the semi-synthesis of SCH 64874 (110) and hirsutellomycin (112) (Scheme [24]).[29] Due to the limited availability of hydrooxepin 108, readily available 104 was chosen as the starting material and hydrolysed to 108. The C2-symmetric epidithiodiketopiperazine alkaloid SCH 64874 (110), was synthesized by condensation of the (–)-deacetylaranotine scaffold with two equivalent of carboxylic acid 109, uncovering the relative stereochemistry of SCH 64874 (110). The relative stereochemistry of the β-keto carboxylic acid chain of the analogous alkaloid hirsutellomycin (112) was determined in a stepwise manner. The C4′–C6′ syn relationships were predicted by comparing the NMR data of the corresponding ester fragments with that of hirsutellomycin (112). The relative stereochemistry of the entire molecule, including the epimerizable C2′ stereocenter was determined by introduction of four diastereomeric side chains into the deacetylaranotin core 108.
Scheme 24 Semi-synthesis of SCH 64874 (110) and hirsutellomycin (112) by Isaka
3.6
Transition-Metal-Catalyzed Cyclization
The natural polyoxygenated dihydrodibenz[b,f]oxepin bulbophylol-B (116) was isolated from Bulbophyllum kwangtungense Schltr (Orchidaceae) by Wu and was shown to display significant cytotoxicity against human epithelial carcinoma (HeLa) and human erythromyeloblastoid leukemia (K562) cells. Additionally, Kitanaka postulated that bulbophylol-B (116) exhibits radical-scavenging activity. Synthesis of bromide 114 commenced with the commercially available benzene-1,2,3-triol (113) and required ten steps (Scheme [25]).[30] Exposure of 114 to different copper catalysts (Cu, Cu2O, CuCl, or CuBr) and potassium carbonate or sodium hydride as base in pyridine at 130 °C only allowed for partial conversion into 115. However, when using soluble copper(I) dimethylsulfide complex as the catalyst at 120 °C, dihydrooxepin 115 was obtained in 89% yield. Cleavage of the benzyl protecting group of 115 via hydrogenolysis employing palladium on charcoal gave the natural product in near-quantitative yield.
Scheme 25 Ullmann coupling for the construction of the dihydrooxepin motif in bulbophylol-B (116) by Kitanaka
Asenapine 122 was discovered and developed by Organon and later co-developed in collaboration with Pfizer. Asenapine (122) is an active ingredient of Saphris® (USA) and Sycrest® (Europe) for the treatment of schizophrenia and acute manic or mixed episodes associated with bipolar disorders. Since the FDA approved the market launch of racemic asenapine in 2009, the most patented and public domain protocols involve the total synthesis of racemic asenapine (122). However, studies of the metabolism and pharmacokinetics of the individual enantiomers of asenapine (122) revealed that the (+)-isomer was found in higher concentrations within the blood plasma compared to the (–)-isomer.
Several synthetic routes for the preparation of asenapine are known today, and the largest reported process scale route is described in Scheme [26].[31] 5-Chloro-2-phenoxyphenylacetic acid (117) was first converted into amide 118. An intramolecular Friedel–Crafts alkylation-dehydration sequence was then performed by subjecting 118 to polyphosphoric acid to afford unsaturated lactam 119 in 62% yield. Reduction of 119 with magnesium in methanol and a catalytic amount of iodine gave a 4:1 diastereomeric mixture of 120 in quantitative yield. Ring-opening of 120 in the presence of potassium hydroxide in refluxing ethanol resulted in concomitant epimerization of the corresponding cis-amino acid to the trans-amino acid 121. Treatment with sodium acetate in refluxing toluene regenerated trans-lactam as a single isomer in 65% yield over three steps. Final lithium aluminum hydride mediated reduction of 121 provided asenapine (122).
Scheme 26 Industrial Friedel–Crafts cyclization for the construction of the dihydrooxepin motif in (±)-asenapine (122)
In 2016, Chandrasekhar published a synthesis of asenapine (122) in optically pure form employing a Ireland–Claisen rearrangement as the key step (Scheme [27]).[32] Starting from commercially available (S)-ethyl lactate 123, chiral pyrrolidine 124 was obtained in twelve steps. The dihydrooxepin ring was closed under Ullmann conditions to afford the desired natural product (+)-asenapine (122) in 71% yield and 94% ee.
Scheme 27 Ullmann coupling for the construction of the dihydrooxepin motif in (+)-asenapine (122) by Chandrasekhar
In 2019, Mlynarski published a shortened asymmetric synthesis of (+)-asenapine (122) (Scheme [28]).[33] Their key step included an organocatalytic Michael addition using aldehyde 125. The final cyclization under the reported Ullmann conditions with pyrrolidine 124 yielded asenapine 122 with >94% ee. The main drawbacks of this approach are the relatively long synthetic process and the need for diazomethane and osmium tetroxide.
Scheme 28 Ullmann coupling for the construction of the dihydrooxepin motif in (+)-asenapine (122) by Mlynarski
The first total synthesis of the dihydrooxepin epidithiodiketopiperazine (–)-acetylaranotin (104) was reported by Reisman and features a rhodium-catalyzed cycloisomerization as the key step (Scheme [29]).[34] At the outset, alkyne 127 was synthesized in ten steps from cinnamaldimine 126. After screening several catalysts and solvents, it was found that exposure of alcohol 127 in N,N-dimethylformamide (DMF) to catalytic bis(1,5-cyclooctadien)dirhodium(I)-dichloride [Rh(cod)-Cl]2 and tris(4-fluorophenyl)phosphine provided the corresponding chlorotetrahydrooxepin 128 in 88% yield. Since all attempts to achieve dimerization of two identical monomers proved to be challenging, a stepwise approach was followed. Elimination was realized by using lithium chloride and lithium carbonate at 100 °C in DMF, yielding the desired dihydrooxepin core.
Scheme 29 Rhodium-catalyzed cycloisomerization for the construction of the dihydrooxepin motif in (–)-acetylaranotin (104) and (–) acetylapoaranotin (131) by Reisman
Subsequent hydrolysis of the ester functionality yielded carboxylic acid 129. In parallel, chemoselective cleavage of the Teoc group in the presence of the TBS ether was achieved by the use of TBAF and allowed for clean formation of the free amine functionality. Subjection of the amine to the previously optimized chloride elimination conditions delivered dihydrooxepin 130 in 55% yield over two steps. Both fragments were combined using classical amide coupling conditions and an additional five steps were required to complete the first enantioselective total synthesis of (–)-acetylaranotin (104).
Further investigations directed toward the implementation of these strategies and methods for the synthesis of related dihydrooxepin-containing natural products resulted in the synthesis of (–)-acetylapoaranotin (131).[35]
The first dihydrooxepin synthesis using a ring-closing metathesis (RCM) was reported by Snieckus in 1998 (Scheme [30]).[36] Carbamate 132 was converted into the desired diene 133 in three steps, which underwent cyclization at high dilution in the presence of Grubbs first-generation catalyst to yield dihydrooxepin 134. A final lithiumaluminium hydride reduction afforded radulanin A (90) in 65% yield.
Scheme 30 Ring-closing metathesis for the construction of the dihydrooxepin motif in radulanin A (90) by Snieckus
In 2007, the first synthesis of heliannuol B (138) was reported by Venkateswaran. Heliannuol B (138) features a unique benzoxepane ring system and belongs to a novel group of allelopathic sesquiterpenes isolated from the cultivar sunflowers Helianthus annus. The synthesis was initiated with phenol 135, which was converted into diene 136 in eleven steps (Scheme [31]).[37] Subsequent RCM yielded the dihydrooxepin 137 in good yield as a mixture of two diastereomers. The crude mixture was directly subjected to an excess of methyl lithium to afford, after chromatographic purification, benzyl protected heliannuol B. Finally, debenzylation using sodium in n-butanol furnished heliannuol B (138).
Scheme 31 Ring-closing metathesis for the construction of the dihydrooxepin motif in heliannuol B (138) by Venkateswaran
In 2014, the first enantioselective total synthesis of heliannuol B (138) was reported by Shishido (Scheme [32]).[38] The key steps include chirality transfer through a Lewis acid-promoted Claisen rearrangement to obtain the tertiary C7 stereocenter and a RCM for assembling the dihydrobenzo[b]oxepin backbone of the natural product. Initial attempts did not give the expected cyclized product but only led to recovered starting material. Same results were obtained in different solvents and at higher temperature. Attempts to reduce the steric bulk by exchanging the carbinol unit with an ester function were unsuccessful. As shown for the synthesis of 141, the limitations of standard RCM protocols forced them to use a relay ring-closing metathesis. Selective debenzylation of 139 followed by allylation of the resulting alcohol provided the allyl ether 140. The addition of Grubbs second-generation catalyst (5 mol%) to a solution of 140 in dichloromethane delivered the functionalized dihydrobenzo[b]oxepin 141 in quantitative yield. Exposure of 141 to aqueous hydrogen chloride yielded heliannuol B (138).
Scheme 32 Ring-closing metathesis for the construction of the dihydrooxepin motif in heliannuol B (138) by Shishido
Radulanins H (146) and E (91) were isolated by Asakawa from the liverwort Radula perrottetii and Radula variabilis. Radulanin H (146) was reported to exhibit calmodulin and cyclooxygenase inhibitory activities. Shishido described a concise total synthesis of radulanin H (146) and the proposed structure of radulanin E (91), utilizing an intramolecular condensation, sequential regioselective allylations, and RCM as the key steps (Scheme [33]).[39] Both routes proceeded by forming the aromatic core from ethyl acetoacetate 143, which was converted into diene 144 in six additional steps. Diene 147 was synthesized in ten steps. Exposure of 144 to RCM using Grubbs second-generation catalyst followed by hydrolysis of the ethyl ester moiety in aqueous potassium hydroxide solution produced radulanin H (146) in 91% yield over two steps.
For the synthesis of 91, exposure of 147 to Grubbs second-generation catalyst afforded the desired dihydrooxepin 148 in 85% yield. Final Pinnick oxidation provided the proposed structure of radulanin E (91) in 74% yield. The structure of 91 was unambiguously confirmed by single-crystal X-ray analysis.
Scheme 33 Ring-closing metathesis for the construction of the dihydrooxepin motif in radulanin H (146) and E (91) by Shishido
Scheme 34 Ring-closing metathesis for the construction of the dihydrooxepin motif in (±)-mycoepoxydiene (154) by Tadano
Mycoepoxydiene (154) was isolated from the fermentation of a rare fungus designated as OS-F66617 in 1999. Its structure and relative stereochemistry were determined by spectral and X-ray crystallographic analyses, but the absolute stereochemistry is still unknown. Tadano published the first synthesis in 2002 via a RCM reaction (Scheme [34]).[40] Starting from racemic anhydride 149 (the Diels–Alder adduct of furan and maleic anhydride), the diene 150 was obtained in eight steps. With diene 150 in hand, the RCM reaction was examined. Treatment of 150 with Grubbs first-generation catalyst (four additions, each of 5 mol% over a period of 20 h) in refluxing benzene furnished the desired oxygen-bridged cyclooctene derivative 151 in 83% yield. Bromination of 151 followed by exposure of the resulting diastereomeric dibromo adduct 152 to potassium tert-butoxide, provided 9-oxabicyclo[4.2.1]nona-2,4-diene derivative 153. The pyranone core was accessed in a further eleven steps and completed the total synthesis of racemic mycoepoxydiene (154).
Scheme 35 Ring-opening/cross/ring-closing metathesis cascade for the construction of the dihydrooxepin motif in (+)-mycoepoxydiene (154), (–)-1893A (159) and (+)-1893b (160) by Tadano
The asymmetric total syntheses of (+)-mycoepoxydiene (154) and the related natural products (–)-1893A (159) and (+)-1893B (160) were reported by Tadano via a one-pot ring-opening/cross/ring-closing metathesis to construct the 9-oxabicyclo[4.2.1]nona-2,4-diene skeleton (Scheme [35]).[41] Starting with the same anhydride, enantioenriched material was obtained by desymmetrization of meso-compounds 149. Intermediate 149 was then converted into alkene 155, which underwent the first ring-opening reaction. Employing Grubbs first-generation catalyst in benzene at 23 °C, the reaction proceeded smoothly to give a mixture of trienes favoring a mixture of the Z-isomers 157 and 158. This mixture was used directly without further purification for the next ring-closing reaction. Interestingly, the Grubbs second-generation catalyst preferentially produced the undesired E-isomers in a diminished yield.
To prevent a competing polymerization of the diene 155, an excess of 1,3-butadiene (156) was employed. The RCM reaction of the mixture of trienes 157 and 158 with Grubbs second-generation catalyst in refluxing benzene afforded the desired dihydrooxepin system together with several unidentified byproducts. Exposure of the mixture to TBAF, gave alcohol 153. To construct the 9-oxabicyclo[4.2.1]nona-2,4-diene unit in a more efficient way, a ROM/CM/RCM one-pot sequence using the alkene 155 was studied. Treatment of 155 with 1,3-butadiene (156) (2 equiv) in the presence of Grubbs first-generation catalyst (2 mol%) in benzene initially produced trienes 157 and 158 at 23 °C. After full consumption of alkene 155, excess 1,3-butadiene (156) was removed by sparging the solution with a stream of argon. Then each 2 mol% of Grubbs second-generation was added in five portions over a period of four days to the refluxing reaction mixture. Desilylation of the reaction mixture provided the key intermediate 153 in 23% yield. With alcohol 153 in hand, the total synthesis of (+)-mycoepoxydiene (154) was accomplished in a further ten steps, (–)-1893A (159) in three steps and (+)-1893B (160) in twelve steps, respectively. Both natural (+)-154 and unnatural (–)-154 were found to show cytotoxicity toward human tumor cells in vitro against human chronic myelogenous leukemia, K562, and against human hepatocellular carcinoma.
Moody reported the synthesis of eranthin (163) and ptaeroxylinol (167) in 2010, which was further used to accomplish the synthesis of the bioactive oxepinochromones obliquumol (164) (angular isomer) and 12-O-acetylptaeroxylinol (168) (linear isomer) by Selepe in 2020 (Scheme [36]).[42] Both synthetic routes use the same strategic RCM reaction and only vary in the choice of different protecting groups. From ketone 97, dienes 161 and 165 were synthesized through a Kostanecki–Robinson reaction, Williamson etherification, and a Claisen rearrangement. Subsequent RCM afforded the desired dihydrooxepins 162 and 166, which then were converted into the natural products eranthin (163) and ptaeroxylinol (167) via desilylation. Acetylation of the free alcohol yielded obliquumol (164) and 12-O-acetylptaeroxylinol (168). The antifungal activities of these compounds were determined against Candida albicans and Cryptococcus neoformans and demonstrated a good to moderate activity against these pathogens.
Scheme 36 Ring-closing metathesis for the construction of the dihydrooxepin motif in obliquumol (164) and 12-O-acetylptaeroxylinol (168) by Selepe
