Coumarin Derivatives from Marine World: Comparison
View Latest Version
Please note this is a comparison between Version 7 by Conner Chen and Version 6 by Conner Chen.

Coumarin and its derivatives have significantly attracted the attention of medicinal chemists and chemical biologists due to their huge range of biological, and in particular, pharmacological properties. Interesting families of coumarins have been found from marine sources, which has accelerated the drug discovery process by inspiring innovation or even by the identification of analogues with remarkable biological properties.

  • coumarin
  • biological activity
  • marine natural products

1. Simple Coumarins

Simple substituted coumarins are the structurally less complex class of coumarins. The scaffold is constituted by a bicyclic system and different substitution patterns at the C-3, C-4, C-5, C-6, C-7 and C-8 positions. Due to the already defined biological activity [1][2], two compounds—umbelliferone (1, R7 = OH) and scopoletin (2, R6 = OCH3 and R7 = OH) —are highlighted here (Figure 1). These molecules were isolated in 2012 from the leaves of the mangrove endophytic fungus Penicillium sp. ZH16 from the South China sea [3].
Figure 1. Simple coumarin derivatives: umbelliferone (1) and scopoletin (2).
Umbelliferone (1) shows anti-inflammatory [4] and antitumoral activities [5]. In 2015, Yu et al. reported the anticancer activity of umbelliferone (1) against HepG2 cancer cells, inducing apoptosis in cells [6], whereas scopoletin (2) inhibits PC3 proliferation, a human prostate cancer cell line [7]. Additionally, both compounds exhibit anti-acetylcholinesterase (AChE) [8][9] and antioxidant activities [10].
As a result of the importance of these scaffolds in organic and medical chemistry, many synthetic routes to obtain simple substituted coumarins have been explored over the years [11][12]. The most classical strategies involve Knoevenagel [13], Pechmann [14] and Perkin [15] condensations, intramolecular [16][17] and intermolecular Wittig reactions [18], ring-closing metathesis [19], as well as different reactions between the corresponding salicylaldehydes with ketene [20] or arylacetonitriles (12) [21] (Scheme 1).
Scheme 1. Synthetic approaches in the preparation of functionalized coumarins.
Over the last few years, transition metal catalysis, involving palladium [22][23], rhodium [24], iron [25] or cobalt [26], has also been used to synthesize different coumarin derivatives. In addition, modern methodologies such as microwave irradiation [27][28], flow chemistry [29], photochemistry [30], ionic liquids [31][32] and organocatalytic reactions [33], proved to be very effective.
For instance, Y. Li et al. employed the photocatalytic isomerization of ortho-E-hydroxycinnamates (13) to generate Z isomers, which underwent lactonization to provide coumarin compounds in high yields (Scheme 2) [34]. A similar strategy was developed by Shu et al. but using Ir2(ppy)4Cl2 as the catalyst (Scheme 2) [35].
Scheme 2. Photocatalytic reactions in the synthesis of coumarins.
Au(I)-catalysts have also been screened to synthesize coumarins by the intramolecular arylation (IMHA) of phenol-derived propiolates (14) [36]. IMHA reactions were carried out using Echavarren’s catalyst (15), (acetonitrile)[(2-biphenyl)di-tert-butylphosphine]gold(I) hexafluoroantimonate, to give numerous derivatized compounds in high yields (Scheme 3).
Scheme 3. Gold(I)-catalyzed reaction in the preparation of coumarin derivatives.
Furthermore, other metal-free methodologies have been reported. In 2016, Lee et al. reported a TfOH-mediated condensation of phenols (16) with propiolic acids (17), followed by intramolecular arylation [37], which was applied to obtain natural umbelliferone (1) in an 81% yield (Scheme 4).
Scheme 4. Metal-free methodology for the preparation of umbelliferone (7).

2. 3-Substituted (Imino- and Amido-) Coumarins

2.1. 3-Iminocoumarins

All 3-iminocoumarins (18–33) reported in the literature have been isolated from mangrove fungi present in the South China sea, along with tens of other metabolites [38]. These compounds do not show relevant biological activity, and no synthetic approaches have been published to date (Figure 2).
Figure 2. Representative examples of iminocoumarins from marine sources.

2.2. 3-Amidocoumarins

Trichodermamide A (34), B (35) and aspergillazine A (36) were the first 3-amidocoumarins isolated at the beginning of the 21st century from different marine-derived fungi, Trichoderma virens and Spicaria elegans [39][40][41]. Spectroscopic analysis and chemical methods (a modified Mosher’s method) allowed for the determination of the structure and stereochemistry of 34 [39] and 36 [42], while the structure of 35 was established by X-ray diffraction analysis (Figure 3) [39].
Figure 3. Representative examples of amidocoumarins from marine sources.
Compounds 34 and 36 proved to display a weak cytotoxic activity against an HL-60 cell line (IC50 = 89 and 84 Μm, respectively) [40]. By contrast, as a result of the presence of the chlorohydrin group in 35, it displays in vitro cytotoxicity against HCT-116 colorectal cancer cells (IC50 = 0.32 μg/mL) [39] and HeLa cells (IC50 = 3.1 μM), by breaking double-stranded DNA [43]. Moreover, weak antimicrobial activities have been reported [41].
Recently, four new 3-amido compounds have been isolated (Figure 4). On the one hand, long-term static fermentation of the strain of Trichoderma sp. TPU199 (cf. Trichoderma brevicompactum) induced the production of dithioaspergillazine A (37), which possesses a disulphide bridge by comparison with spectroscopic data. In contrast to aspergillazine A (36), the compound inhibits the proliferation of the colon cancer HCT-15 cell line (IC50 = 13 μM) and Jurkat leukemia cells (IC50 = 1.3 μM) [44]. On the other hand, trichodermamide C (38) and hatsumamide A (39) and B (40) were isolated from the deep sea-derived fungus Penicillium steckii FKJ-0213 by physicochemical (PC) screening [45]. The structure of 38, which also contains a 1,2-oxazine system, was previously established by NMR, UV, IR, MS and X-ray diffraction data. It shows moderate cytotoxic effects towards human colorectal carcinoma HCT116 (IC50 = 0.68 μg/mL) and human lung carcinoma A549 (IC50 = 4.28 μg/mL) [46]. The structure and stereochemistry of 39 and 40 were elucidated by mass spectrometry, 1D and 2D NMR data (COSY, HMQC, HMBC and ROESY) and by comparing data with other already known compounds. No biological activity of 40 has been reported. However, 39 presents antimalarial activity against the K1 and FCR3 strains of Plasmodium falciparum, with IC50 values of 27.2 an 27.9 μM, respectively, and cytotoxicity against five human tumor cell lines, HeLa S3 (IC50 = 15.0 μM), HT29 (IC50 = 6.8 μM), A549 (IC50 = 13.7 μM), H1299 (IC50 = 18.7 μM) and Panc1 (IC50 = 12.9 μM) [45].
Figure 4. Other examples of amidocoumarins from marine sources.
Trichodermamides 34, 35 and 36 could be disconnected into two fragments: an oxazine ring moiety 41 and an aminocoumarin 42 (Scheme 5). Different synthetic strategies have been developed in order to afford the 4H-5,6-dihydro-1,2-oxazine fragment 41.
Scheme 5. Retrosynthetic analysis for the preparation of trichodermamides.
In 2008, Joullié and Wan described the total synthesis of 34 and 35 [47]. Thus, the advanced intermediate 46, obtained in 18 linear steps from (–)-quinic acid 43, was treated with hydroxylamine to obtain an oxime, which in situ underwent an intramolecular epoxide ring opening upon addition of NaOH. Oxazine 47, obtained as a single diastereomer, was then converted (over four reaction steps) into enone 48. A Luche reduction followed by selective primary alcohol oxidation provided acid 49 in a good yield (Scheme 6).
Scheme 6. Methodology for the preparation of fragment G.
The coupling reaction between carboxylic acid 49 and aminocoumarin B (obtained in three steps from 3,4-trimethoxy-benzaldehyde) was performed using EDCI in 30% pyridine/dichloromethane. Compound 34 was obtained after coupling and two deprotection steps in a 53% yield, while 35 required an additional treatment with mesyl chloride in order to obtain the corresponding allylic chloride (32% over four reaction steps). The total enantioselective syntheses were achieved in 31/32 reaction steps, with an average of an 85% yield for each reaction step (Scheme 7) [47].
Scheme 7. Final steps of the synthesis of trichodermamides A (34) and B (35).
More recently, a new concise total synthesis of trichodermamides A, B and C has been described [48]. A 1,2-addition of an αC-lithiated O-silyl ethyl pyruvate oxime 51 to benzoquine 52, followed by an oxa-Michael ring closure was applied to accomplish the formation of the cis-fused 1,2-oxazadecaline core 53 in a 92% yield. A modified Luche reduction and treatment with Pd(PPh3)4 in the presence of N,O-bis-(trimethylsilyl)acetamide (BTSA) was carried out to give dienol 54 in a high yield, a common intermediate in the synthesis of the three natural products (Scheme 8).
Scheme 8. Methodology for the preparation of fragment 54.
Once the oxazadecaline 54 was obtained, similar chemical steps, but arranged in different order, provided the three natural compounds. In these syntheses, the two key steps are the amide coupling, mediated by HATU in the presence of sym-collidine, and a final selenoxide [49][50]-sigmatropic rearrangement with H2O2 in pyridine [51], which was previously used by Zakarian and Lu [52]. Trichodermamides 34, 35 and 40 have been obtained after 9, 12 or 13 steps, respectively, in moderate yields (Scheme 9).
Scheme 9. Synthetic methodology for the preparation of trichodermamides A (34), B (35) and C (40).
No synthetic approach for 36, 37, 39 and 40 has been reported yet.

3. Tricyclic Coumarins

3.1. Furocoumarins

First, furocoumarins (also called psoralenes) are described as coumarin derivatives with a fused furan ring with important biological activities, such as photoreactivity with DNA [53]. Four structures of furo[g]coumarins (60–63) were found in the endophytic fungus Penicillium sp. ZH16 from the South China sea (Figure 5) [3].
Figure 5. Examples of furocoumarins from marine sources.
From this series, the derivative 62 was tested against KB and KBV200 cells demonstrating relevant cytotoxicity (IC50 of 5 and 10 μg/mL, respectively). In addition, 63 shows interesting photochemotherapeutic effects under near UV and blue light photosensitization (LD50 of 2 nM and 12 nM, respectively). These cytotoxic studies suggest the possibility of furocoumarins being involved in the high incidence of cancer in Nigeria [54].
The synthesis of furocoumarins has been known for a long time. However, novel methodologies have been developed during the last decades for the effective preparation of these compounds, many of which involve metal-catalyzed transformations that provide new structural diversity [55][56].
One such example has been the preparation of bergaptene (61). Although it was first isolated in 1834, it was not until 1936 when the first synthetic approach was described. Then, other methodologies were developed during the next decades [57]. Recently, Zhimin et al. reported a new synthesis of 61 in a higher isolated yield (55%) compared to the reported methodologies. Following known methodologies, phloroglucinol was used as the starting material to construct benzofuran-3-one 66 (by monomethylation and Pechmann reactions). Various conventional steps (acetylation, deacetylation) provided the intermediate 69 from which a fused lactone ring was constructed by acetylation and Pechmann condensation. A final dehydrogenation step with DDQ provided the final product 61 (Scheme 10).
Scheme 10. Synthetic methodology for the preparation of bergaptene (61).

3.2. Benzo[c]coumarins

Benzocoumarins are π-extended structures in which the coumarin core is fused with a benzene ring at different positions. Four benzo[c]coumarins (71–74, 3,4-benzocoumarins or alternariol derivatives) have been found from ocean sources, produced by the mangrove endophytic fungus No. 2240, from the South China sea coast (Figure 6) [58]. The structures were determined by spectroscopic analysis using NMR, IR and UV experiments and by comparison with the literature data.
Figure 6. Examples of benzo[c]coumarins.
Alternariol (71, R1 = R2 = OH) and its derivatives (72–74) have demonstrated mutagenic properties against the human epidermoic carcinoma KB and KBv200 cell lines. In particular, 71 and 74 show stronger IC50 values (3.17, 3.12 and 4.82, 4.94 μg/mL, respectively) in both cell lines, in comparison with the weaker activities found for the other compounds (IC50 > 50 μg/mL).
The construction of benzocoumarins depends on the location of hydroxyl and formyl groups on the starting material, which is normally hydroxynaphthaldehyde. Many complementary strategies have been reported for the general synthesis of benzo[c]coumarin derivatives, which are based on carbon–carbon and carbon–oxygen bond formation strategies or cyclization reactions [59].
A total synthesis of 71 was described independently by the Podlech and Kim groups [60][61]. The key step in both protocols was a Suzuki–Miyaura cross-coupling of boronic acid 75 with a brominated aldehyde 76 to obtain an advanced precursor 77. A final cyclization step was needed to obtain the final product 71 (Scheme 11).
Scheme 11. Critical key step in the total synthesis of alternariol (77).
More recently, the most common techniques in the synthesis of general benzo[c]coumarins have been the oxidative cyclization of biphenyl-2-carboxylic acid compounds [62] and Hurtley condensation [63]. However, other strategies that generate chemical diversity have been applied to obtain highly functionalized benzco[c]coumarins. For instance, Bodwell et al. prepared a set of benzo[c]coumarins by an inverse electron demand Diels–Alder reaction [64]. Later on, a multicomponent version (93, 784 and 8579) comprising 6 reaction steps and increasing chemical diversity was disclosed by the same groups (Scheme 12) [65].
Scheme 12. Multistep synthesis of benzo[c]coumarins.
Later, Lee’s group reported the reaction of hydroxychalcones (860) and β-ketoesters (871), in the presence of a base, in sequential Michael addition/intramolecular aldol condensation/oxidative aromatization/lactonization processes (Scheme 13) [66].
Scheme 13. Domino reaction process for the synthesis of benzo[c]coumarins.

3.3. Other Tricyclic Coumarins

In addition to the previously mentioned groups, other tricyclic coumarins have been found in marine organisms. The limited number of their structural features does not allow for their classification in a particular group. Two pyrano[g]coumarins were isolated from Streptomyces violans bacteria and Ascomycete Leptosphaeria oraemaris fungi (compounds 87 1 and 882, respectively). In addition, iotrochotazine A (893) was found in the marine sponge Iotrochota sp. in Australia, and it is used as chemical probe to study Parkinson’s disease [67]. A series of dihydrocoumarins (9084–895) was also found in Rhizophora stylosa mangrove trees in Okinawa, Japan. These compounds present DPPH free radical scavenging properties (EC50 4.6–10.3 μM) and serve as traditional medicine for the local people due to their antioxidant activities (Figure 7) [68][69].
Figure 7. Examples of tricyclic coumarins found from marine sources.
There are not many protocols reported for the preparation of each of these scaffolds. For instance, cinchonain derivatives 92 86 and 93 87 were successfully synthetized by the Kadota group, in a one-pot regioselective procedure involving a dienone–phenol rearrangement followed by a Michael-type reaction (Scheme 14) [70].
Scheme 14. Synthesis of cinchonain.
Considering 893, a total synthesis was developed in 2014 through a one-pot enamine formation/intramolecular conjugate addition/oxidation sequence. The confirmation of the natural product allowed for subsequent biological investigations (Scheme 15) [67].
Scheme 15. Synthesis of iotrochotazine A.

References

  1. Tsivileva, O.M.; Koftin, O.V.; Evseeva, N.V. Coumarins as Fungal Metabolites with Potential Medicinal Properties. Antibiotics 2022, 11, 1156.
  2. Garg, S.S.; Gupta, J.; Sharma, S.; Sahu, D. An insight into the therapeutic applications of coumarin compounds and their mechanisms of action. Eur. J. Pharm. Sci. 2020, 152, 105424.
  3. Huang, Z.; Yang, J.; Cai, X.; She, Z.; Lin, Y. A new furanocoumarin from the mangrove endophytic fungus Penicillium sp. (ZH16). Nat. Prod. Res. 2012, 26, 1291–1295.
  4. Lino, C.; Taveira, M.; Viana, G.; Matos, F. Analgesic and antiinflammatory activities of Justicia pectoralis Jacq and its main constituents: Coumarin and umbelliferone. Phytother. Res. 1997, 11, 211–215.
  5. Stefanova, T.H.; Nikolova, N.J.; Toshkova, R.A.; Neychev, H.O. Antitumor and immunomodulatory effect of coumarin and 7-hydroxycoumarin against Sarcoma 180 in mice. J. Exp. Ther. Oncol. 2007, 6, 107–115.
  6. Yu, S.M.; Hu, D.H.; Zhang, J.J. Umbelliferone exhibits anticancer activity via the induction of apoptosis and cell cycle arrest in HepG2 hepatocellular carcinoma cells. Mol. Med. Rep. 2015, 12, 3869–3873.
  7. Liu, X.L.; Zhang, L.; Fu, X.L.; Chen, K.; Qian, B.C. Effect of scopoletin on PC3 cell proliferation and apoptosis. Acta Pharmacol. Sin. 2001, 22, 929–933.
  8. Hornick, A.; Lieb, A.; Vo, N.P.; Rollinger, J.M.; Stuppner, H.; Prast, H. The coumarin scopoletin potentiates acetylcholine release from synaptosomes, amplifies hippocampal long-term potentiation and ameliorates anticholinergic- and age-impaired memory. Neuroscience 2011, 197, 280–292.
  9. Anand, P.; Singh, B.; Singh, N. A review on coumarins as acetylcholinesterase inhibitors for Alzheimer’s disease. Biorg. Med. Chem. 2012, 20, 1175–1180.
  10. Kostova, I.; Bhatia, S.; Grigorov, P.; Balkansky, S.; Parmar, V.S.; Prasad, A.K.; Saso, L. Coumarins as antioxidants. Curr. Med. Chem. 2011, 18, 3929–3951.
  11. Salem, M.A.; Helal, M.H.; Gouda, M.A.; Ammar, Y.A.; El-Gaby, M.S.A.; Abbas, S.Y. An overview on synthetic strategies to coumarins. Synth. Commun. 2018, 48, 1534–1550.
  12. Venugopala, K.N.; Rashmi, V.; Odhav, B. Review on natural coumarin lead compounds for their pharmacological activity. BioMed Res. Int. 2013, 2013, 963248.
  13. Shakil, M.R.; Meguerdichian, A.G.; Tasnim, H.; Shirazi-Amin, A.; Seraji, M.S.; Suib, S.L. Syntheses of ZnO with Different Morphologies: Catalytic Activity toward Coumarin Synthesis via the Knoevenagel Condensation Reaction. Inorg. Chem. 2019, 58, 5703–5714.
  14. Zhang, S.; Tan, X.; Liang, C.; Zhang, W. Design, synthesis, and antifungal evaluation of novel coumarin-pyrrole hybrids. J. Heterocycl. Chem. 2021, 58, 450–458.
  15. Augustine, J.K.; Bombrun, A.; Ramappa, B.; Boodappa, C. An efficient one-pot synthesis of coumarins mediated by propylphosphonic anhydride (T3P) via the Perkin condensation. Tetrahedron Lett. 2012, 53, 4422–4425.
  16. Belavagi, N.S.; Deshapande, N.; Sunagar, M.G.; Khazi, I.A.M. A practical one-pot synthesis of coumarins in aqueous sodium bicarbonate via intramolecular Wittig reaction at room temperature. RSC Adv. 2014, 4, 39667–39671.
  17. Upadhyay, P.K.; Kumar, P. A novel synthesis of coumarins employing triphenyl(α-carboxymethylene)phosphorane imidazolide as a C-2 synthon. Tetrahedron Lett. 2009, 50, 236–238.
  18. Pünkösti, Z.; Kele, P.; Herner, A. Synthesis of 7-Azido-3-Formylcoumarin—A Key Precursor in Bioorthogonally Applicable Fluorogenic Dye Synthesis. J. Heterocycl. Chem. 2018, 55, 1183–1188.
  19. Polito, L.; Cravini, M.; Poletti, L.; Lay, L. Simple Synthesis of Versatile Coumarin Scaffolds. Synth. Commun. 2006, 36, 2203–2209.
  20. Chandrasekhar, S.; Kumar, H.V. An Expeditious Coumarin Synthesis via a “Pseudocycloaddition” Between Salicylaldehydes and Ketene. Synth. Commun. 2015, 45, 232–235.
  21. Li, C.; Zhu, H.; Zhang, H.; Yang, Y.; Wang, F. Synthesis of 2H-Chromenones from Salicylaldehydes and Arylacetonitriles. Molecules 2017, 22, 1197.
  22. Sharma, U.; Naveen, T.; Maji, A.; Manna, S.; Maiti, D. Palladium-Catalyzed Synthesis of Benzofurans and Coumarins from Phenols and Olefins. Angew. Chem. Int. Ed. 2013, 52, 12669–12673.
  23. Wienhold, M.; Molloy, J.J.; Daniliuc, C.G.; Gilmour, R. Coumarins by Direct Annulation: β-Borylacrylates as Ambiphilic C3-Synthons. Angew. Chem. Int. Ed. 2021, 133, 695–699.
  24. Gadakh, S.K.; Dey, S.; Sudalai, A. Rh-Catalyzed Synthesis of Coumarin Derivatives from Phenolic Acetates and Acrylates via C–H Bond Activation. J. Org. Chem. 2015, 80, 11544–11550.
  25. Kutubi, M.S.; Hashimoto, T.; Kitamura, T. Improved Synthesis of Coumarins by Iron(III)-Catalyzed Cascade Reaction of Propiolic Acids and Phenols. Synthesis 2011, 2011, 1283–1289.
  26. Liu, X.-G.; Zhang, S.-S.; Jiang, C.-Y.; Wu, J.-Q.; Li, Q.; Wang, H. Cp*Co(III)-Catalyzed Annulations of 2-Alkenylphenols with CO: Mild Access to Coumarin Derivatives. Org. Lett. 2015, 17, 5404–5407.
  27. Fiorito, S.; Epifano, F.; Taddeo, V.A.; Genovese, S. Ytterbium triflate promoted coupling of phenols and propiolic acids: Synthesis of coumarins. Tetrahedron Lett. 2016, 57, 2939–2942.
  28. Konrádová, D.; Kozubíková, H.; Doležal, K.; Pospíšil, J. Microwave-Assisted Synthesis of Phenylpropanoids and Coumarins: Total Synthesis of Osthol. Eur. J. Org. Chem. 2017, 2017, 5204–5213.
  29. Li, X.; Chen, A.; Zhou, Y.; Huang, L.; Fang, Z.; Gan, H.; Guo, K. Two-stage flow synthesis of coumarin via O-acetylation of salicylaldehyde. J. Flow Chem. 2015, 5, 82–86.
  30. Zhao, B.; Xu, B. Visible-light promoted oxidative cyclization of cinnamic acid derivatives using xanthone as the photocatalyst. Org. Biomol. Chem. 2021, 19, 568–573.
  31. Valizadeh, H.; Vaghefi, S. One-Pot Wittig and Knoevenagel Reactions in Ionic Liquid as Convenient Methods for the Synthesis of Coumarin Derivatives. Synth. Commun. 2009, 39, 1666–1678.
  32. Prabhala, P.; Savanur, H.M.; Sutar, S.M.; Malunavar, S.S.; Kalkhambkar, R.G.; Laali, K.K. Facile one-pot synthetic access to libraries of diversely substituted 3-aryl (Alkyl)-coumarins using ionic liquid (IL) or conventional base/solvent, and an IL-mediated approach to novel coumarin-bearing diaryl-ethynes. Tetrahedron Lett. 2020, 61, 151854.
  33. Wei, J.; Wang, P.; Jia, Q.; Huang, J.; Du, Z.; Zhang, K.; Wang, J. Amine-Catalyzed Cascade Synthesis of 3,4-Diunsubstituted Coumarins. Eur. J. Org. Chem. 2013, 2013, 4499–4502.
  34. Zhan, K.; Li, Y. Visible-Light photocatalytic E to Z isomerization of activated olefins and its application for the syntheses of coumarins. Catalysts 2017, 7, 337.
  35. Shu, P.; Xu, H.; Zhang, L.; Li, J.; Liu, H.; Luo, Y.; Yang, X.; Ju, Z.; Xu, Z. Synthesis of (Z)-Cinnamate Derivatives via Visible-Light-Driven E-to-Z Isomerization. SynOpen 2019, 03, 103–107.
  36. Cervi, A.; Vo, Y.; Chai, C.L.L.; Banwell, M.G.; Lan, P.; Willis, A.C. Gold(I)-Catalyzed Intramolecular Hydroarylation of Phenol-Derived Propiolates and Certain Related Ethers as a Route to Selectively Functionalized Coumarins and 2H-Chromenes. J. Org. Chem. 2021, 86, 178–198.
  37. Choi, H.; Kim, J.; Lee, K. Metal-free, Brønsted acid-mediated synthesis of coumarin derivatives from phenols and propiolic acids. Tetrahedron Lett. 2016, 57, 3600–3603.
  38. Tao, L.-y.; Zhang, J.-y.; Liang, Y.-j.; Chen, L.-m.; Zheng, L.-s.; Wang, F.; Mi, Y.-j.; She, Z.-g.; To, K.K.W.; Lin, Y.-c.; et al. Anticancer Effect and Structure-Activity Analysis of Marine Products Isolated from Metabolites of Mangrove Fungi in the South China Sea. Mar. Drugs 2010, 8, 1094–1105.
  39. Garo, E.; Starks, C.M.; Jensen, P.R.; Fenical, W.; Lobkovsky, E.; Clardy, J. Trichodermamides A and B, Cytotoxic Modified Dipeptides from the Marine-Derived Fungus Trichoderma virens. J. Nat. Prod. 2003, 66, 423–426.
  40. Liu, R.; Gu, Q.-Q.; Zhu, W.-M.; Cui, C.-B.; Fan, G.-T. Trichodermamide A and aspergillazine A, two cytotoxic modified dipeptides from a marine-derived fungus Spicaria elegans. Arch. Pharmacal. Res. 2005, 28, 1042–1046.
  41. Wang, Y.; Lu, Z.; Sun, K.; Zhu, W. Effects of High Salt Stress on Secondary Metabolite Production in the Marine-Derived Fungus Spicaria elegans. Mar. Drugs 2011, 9, 535–542.
  42. Capon, R.J.; Ratnayake, R.; Stewart, M.; Lacey, E.; Tennant, S.; Gill, J.H. Aspergillazines A–E: Novel heterocyclic dipeptides from an Australian strain of Aspergillus unilateralis. Org. Biomol. Chem. 2005, 3, 123–129.
  43. Jans, P.E.; Mfuh, A.M.; Arman, H.D.; Shaffer, C.V.; Larionov, O.V.; Mooberry, S.L. Cytotoxicity and Mechanism of Action of the Marine-Derived Fungal Metabolite Trichodermamide B and Synthetic Analogues. J. Nat. Prod. 2017, 80, 676–683.
  44. Yamazaki, H.; Rotinsulu, H.; Takahashi, O.; Kirikoshi, R.; Namikoshi, M. Induced production of a new dipeptide with a disulfide bridge by long-term fermentation of marine-derived Trichoderma cf. brevicompactum. Tetrahedron Lett. 2016, 57, 5764–5767.
  45. Matsuo, H.; Hokari, R.; Ishiyama, A.; Iwatsuki, M.; Higo, M.; Nonaka, K.; Nagano, Y.; Takahashi, Y.; Ōmura, S.; Nakashima, T. Hatsusamides A and B: Two New Metabolites Produced by the Deep-Sea-Derived Fungal Strain Penicillium steckii FKJ-0213. Mar. Drugs 2020, 18, 513.
  46. Davis, R.A.; Longden, J.; Avery, V.M.; Healy, P.C. The isolation, structure determination and cytotoxicity of the new fungal metabolite, trichodermamide C. Bioorg. Med. Chem. Lett. 2008, 18, 2836–2839.
  47. Wan, X.; Joullié, M.M. Enantioselective Total Syntheses of Trichodermamides A and B. J. Am. Chem. Soc. 2008, 130, 17236–17237.
  48. Mfuh, A.M.; Zhang, Y.; Stephens, D.E.; Vo, A.X.T.; Arman, H.D.; Larionov, O.V. Concise Total Synthesis of Trichodermamides A, B, and C Enabled by an Efficient Construction of the 1,2-Oxazadecaline Core. J. Am. Chem. Soc. 2015, 137, 8050–8053.
  49. Fernández-Peña, L.; Díez-Poza, C.; González-Andrés, P.; Barbero, A. The Tetrahydrofuran Motif in Polyketide Marine Drugs. Mar. Drugs 2022, 20, 120.
  50. Boström, J.; Brown, D.G.; Young, R.J.; Keserü, G.M. Expanding the medicinal chemistry synthetic toolbox. Nat. Rev. Drug Discov. 2018, 17, 709–727.
  51. Reich, H.J. Organoselenium chemistry. Synthetic transformations based on allyl selenide anions. J. Org. Chem. 1975, 40, 2570–2572.
  52. Lu, C.-D.; Zakarian, A. Total Synthesis of (±)-Trichodermamide B and of a Putative Biosynthetic Precursor to Aspergillazine A Using an Oxaza-Cope Rearrangement. Angew. Chem. Int. Ed. 2008, 47, 6829–6831.
  53. Santana, L.; Uriarte, E.; Roleira, F.; Milhazes, N.; Borges, F. Furocoumarins in medicinal chemistry. Synthesis, natural occurrence and biological activity. Curr. Med. Chem. 2004, 11, 3239–3261.
  54. Uwaifo, A.O.; Billings, P.C.; Heidelberger, C. Mutation of Chinese Hamster V79 Cells and Transformation and Mutation of Mouse Fibroblast C3H/10T½ Clone 8 Cells by Aflatoxin B1 and Four Other Furocoumarins Isolated from Two Nigerian Medicinal Plants. Cancer Res. 1983, 43, 1054–1058.
  55. Cadierno, V. Metal-catalyzed routes for the synthesis of furocoumarins and coumestans. In Green Synthetic Approaches for Biologically Relevant Heterocycles; Elsevier: Amsterdam, The Netherlands, 2021; pp. 53–96.
  56. Rao, M.L.; Nand, S.; Murty, V.N. Metal-Catalyzed Divergent Synthetic Methods for Pyrrolocoumarins and Furocoumarins. Asian J. Org. Chem. 2022, 11, e202100604.
  57. Cai, X.; Ji, D.; Liu, J.; Hu, M.; Jin, Z. A New Approach to the Synthesis of Bergapten. Chem. Res. Chin. Univ. 2022, 31, 1–5.
  58. Tan, N.; Tao, Y.; Pan, J.; Wang, S.; Xu, F.; She, Z.; Lin, Y.; Gareth Jones, E. Isolation, structure elucidation, and mutagenicity of four alternariol derivatives produced by the mangrove endophytic fungus No. 2240. Chem. Nat. Compd. 2008, 44, 296–300.
  59. Jasim, S.; Mustafa, Y. A Review of Classical and Advanced Methodologies for Benzocoumarin Synthesis. J. Med. Chem. Sci. 2022, 5, 676–694.
  60. Koch, K.; Podlech, J.; Pfeiffer, E.; Metzler, M. Total synthesis of alternariol. J. Org. Chem. 2005, 70, 3275–3276.
  61. Won, M.; Kwon, S.; Kim, T.-H. An efficient synthesis of alternariol. J. Korean Chem. Soc. 2015, 59, 471–474.
  62. Gallardo-Donaire, J.; Martin, R. Cu-catalyzed mild C (sp2)–H functionalization assisted by carboxylic acids en route to hydroxylated arenes. J. Am. Chem. Soc. 2013, 135, 9350–9353.
  63. Krzeszewski, M.; Vakuliuk, O.; Gryko, D.T. Color-tunable fluorescent dyes based on benzo coumarin. Eur. J. Org. Chem. 2013, 2013, 5631–5644.
  64. Pottie, I.R.; Nandaluru, P.R.; Benoit, W.L.; Miller, D.O.; Dawe, L.N.; Bodwell, G.J. Synthesis of 6 H-Dibenzo pyran-6-ones Using the Inverse Electron Demand Diels–Alder Reaction. J. Org. Chem. 2011, 76, 9015–9030.
  65. Nandaluru, P.R.; Bodwell, G.J. Multicomponent Synthesis of 6 H-Dibenzo pyran-6-ones and a Total Synthesis of Cannabinol. Org. Lett. 2012, 14, 310–313.
  66. Poudel, T.N.; Lee, Y.R. An advanced and novel one-pot synthetic method for diverse benzo chromen-6-ones by transition-metal free mild base-promoted domino reactions of substituted 2-hydroxychalcones with β-ketoesters and its application to polysubstituted terphenyls. Org. Biomol. Chem. 2014, 12, 919–930.
  67. Grkovic, T.; Pouwer, R.H.; Vial, M.L.; Gambini, L.; Noël, A.; Hooper, J.N.; Wood, S.A.; Mellick, G.D.; Quinn, R.J. NMR Fingerprints of the Drug-like Natural-Product Space Identify Iotrochotazine A: A Chemical Probe to Study Parkinson’s Disease. Angew. Chem. Int. Ed. 2014, 53, 6070–6074.
  68. Takara, K.; Kuniyoshi, A.; Wada, K.; Kinjyo, K.; Iwasaki, H. Antioxidative flavan-3-ol glycosides from stems of Rhizophora stylosa. Biosci. Biotechnol. Biochem. 2008, 72, 2191–2194.
  69. Bandaranayake, W.M. Bioactivities, bioactive compounds and chemical constituents of mangrove plants. Wetl. Ecol. Manag. 2002, 10, 421–452.
  70. Awale, S.; Tezuka, Y.; Wang, S.; Kadota, S. Facile and regioselective synthesis of phenylpropanoid-substituted flavan-3-ols. Org. Lett. 2002, 4, 1707–1709.
More
© Text is available under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/)
Video Production Service
Feedback