References
- (a) Victor, M. M.; Riatto, V. B.; Pilli, R. A.; Fifteen Years of Biological and Synthetic Studies of Decarestrictine Family. Tetrahedron 2008, 64, 2279–2300. DOI: https://doi.org/10.1016/j.tet.2007.11.034. (b) Ratnayake, A. S.; Yoshida, W. Y.; Mooberry, S. L.; Hemscheidt, T. The Structure of Microcarpalide, a Microfilament Disrupting Agent from an Endophytic Fungus. Org. Lett. 2001, 3, 3479–3481. DOI: https://doi.org/10.1021/ol016515s. (c) Furstner, A.; Radkowski, K. Enantioselective Total Synthesis of the Phytotoxic Lactone Herbarumin I. Chem. Commun. 2001, 2001, 671–672. DOI: https://doi.org/10.1039/b101148k. (d) Bodo, B.; Molho, L.; Davoust, D.; Molho, D. Fungal Macrolides: Structure Determination and Biosynthesis of Achaetolide, a Lactone from Achaetomium Cristalliferum. Phytochemistry 1983, 22, 447–451. [Mismatch] DOI: https://doi.org/10.1016/0031-9422(83)83021-0.
- Gohrt, A.; Zeeck, A.; Hutter, K.; Kirsch, R.; Kluge, H.; Thiericke, R. Secondary Metabolites by Chemical Screening. 9. Decarestrictines, a New Family of Inhibitors of Cholesterol Biosynthesis from Penicillium. II. Structure Elucidation of the Decarestrictines A to D. J. Antibiot. 1992, 45, 66–73. DOI: https://doi.org/10.7164/antibiotics.45.66.
- Grabley, S.; Granzer, E.; Hutter, K.; Ludwig, D.; Mayer, M.; Thiericke, R.; Till, G.; Wink, J.; Philipps, S.; Zeeck, A. Secondary Metabolites by Chemical Screening. 8. Decarestrictines, a New Family of Inhibitors of Cholesterol Biosynthesis from Penicillium. I. Strain Description, Fermentation, Isolation and Properties. J. Antibiot. 1992, 45, 56–65. DOI: https://doi.org/10.7164/antibiotics.45.56.
- Grabley, S.; Hammann, P.; Hutter, K.; Kirsch, R.; Kluge, H.; Thiericke, R.; Mayer, M.; Zeeck, A. SECONDARY METABOLITES by CHEMICAL SCREENING. 20. Decarestrictines, a New Family of Inhibitors of Cholesterol Biosynthesis from Penicillium: III. Decarestrictines E to M. J. Antibiot. 1992, 45, 1176–1181. DOI: https://doi.org/10.7164/antibiotics.45.1176.
- Mayer, M.; Thiericke, R. A Non-Enzymatic Reaction in the Late Biosynthesis of the Decarestrictine Family. J. Antibiot. 1993, 46, 1372–1380. DOI: https://doi.org/10.7164/antibiotics.46.1372.
- Rukachaisirikul, V.; Pramjit, S.; Pakawatchai, C.; Isaka, M.; Supothina, S. 10-membered Macrolides from the Insect Pathogenic Fungus Cordyceps militaris BCC 2816. J. Nat. Prod. 2004, 67, 1953–1955. DOI: https://doi.org/10.1021/np0401415.
- Drager, G.; Kirschning, A.; Thiericke, R.; Zerlin, M. Decanolides, 10-Membered Lactones of Natural Origin. Nat. Prod. Rep. 1996, 13, 365–375. DOI: https://doi.org/10.1039/NP9961300365.
- Stierle, A. A.; Stierle, D. B.; Decato, D.; Priestley, N. D.; Alverson, J. B.; Hoody, J.; McGrath, K.; Klepacki, D. The Berkeleylactones, Antibiotic Macrolides from Fungal Coculture. J. Nat. Prod. 2017, 80, 1150–1160. DOI: https://doi.org/10.1021/acs.jnatprod.7b00133.
- Reddy, M. S.; Manikanta, G.; Krishna, P. R. First Stereoselective Total Synthesis of Antibiotic Macrolide Berkeleylactone F. Tetrahedron Lett. 2019, 60, 504–506. DOI: https://doi.org/10.1016/j.tetlet.2019.01.017.
- Subba, S.; Saha, S.; Mandal, S. S. A Diastereoselective Synthetic Approach towards the Synthesis of Berkeleylactone F and Its 4-epi-Derivative. Open 2020, 04, 66–70. DOI: https://doi.org/10.1055/s-0040-1707305.
- Jung, J. C.; Rajashaker, K.; Vines, K. K.; Zheng, Y. S.; Bijoy, P.; Muralikrishna, V.; Avery, M. A. Total Syntheses of Epothilones B and d. J. Org. Chem. 2004, 69, 9269–9284. DOI: https://doi.org/10.1021/jo048742o.
- Gwon, G. B.; Jung, H. G.; Seu, Y. B. Chiral Synthesis of Natural (+)‐ Endo-Brevicomin with Enzymatic Reaction from l-Tartaric Acid. Bull. Korean Chem. Soc. 2019, 40, 1150–1151. DOI: https://doi.org/10.1002/bkcs.11893.
- Mozingo, R.; Wolf, D. E.; Harris, S. A.; Folkers, K. Hydrogenolysis of Sulfur Compounds by Raney Nickel Catalyst. J. Am. Chem. Soc. 1943, 65, 1013–1016. DOI: https://doi.org/10.1021/ja01246a005.
- Inanaga, J.; Hirata, K.; Saeki, H.; Katsuki, T.; Yamaguchi, M. A Rapid Esterification by Means of Mixed Anhydride and Its Application to Large-Ring Lactonization. BCSJ 1979, 52, 1989–1993. DOI: https://doi.org/10.1246/bcsj.52.1989.