Multiple hydride reduction pathways in isoflavonoids

Scholarly Works

• Liu, C.-H.; Xu, M.; Luo, Q.; Wang, Z.; Tan, W.; Zhao, X.; Jia, X. Inexpensive and mild hydrogenation condition: Raney Ni-catalyzed reduction of alkenes and alkynes using Et3SiH at ambient temperature. Tetrahedron 2024, 160, 134040. doi:10.1016/j.tet.2024.134040
• Heo, M.; Lee, B.; Sishtla, K.; Fei, X.; Lee, S.; Park, S.; Yuan, Y.; Lee, S. K.; Kwon, S.; Lee, J.; Kim, S.; Corson, T. W.; Seo, S.-Y. Enantioselective Synthesis of Homoisoflavanones by Asymmetric Transfer Hydrogenation and Their Biological Evaluation for Antiangiogenic Activity. The Journal of organic chemistry 2019, 84, 9995–10011. doi:10.1021/acs.joc.9b01134
• Poonam; Kumari, P.; Grishina, M.; Potemkin, V.; Verma, A.; Rathi, B. Oxygen mediated highly efficient cobalt(II) porphyrin-catalyzed reduction of functional chromones: experimental and computational studies. New Journal of Chemistry 2019, 43, 5228–5238. doi:10.1039/c9nj00266a
• Xu, L.; Gordon, R. R.; Farmer, R. L.; Pattanayak, A.; Binkowski, A.; Huang, X.; Avram, M. J.; Krishna, S. N.; Voll, E.; Pavese, J. M.; Chavez, J. D.; Bruce, J. E.; Mazar, A. P.; Nibbs, A. E.; Anderson, W. F.; Li, L.; Jovanovic, B.; Pruell, S.; Valsecchi, M.; Francia, G.; Betori, R. C.; Scheidt, K. A.; Bergan, R. C. Precision therapeutic targeting of human cancer cell motility. Nature communications 2018, 9, 2454. doi:10.1038/s41467-018-04465-5
• Qin, T.; Metz, P. Enantioselective Synthesis of Isoflavanones by Catalytic Dynamic Kinetic Resolution. Organic letters 2017, 19, 2981–2984. doi:10.1021/acs.orglett.7b01218
• Lee, H.; Yuan, Y.; Rhee, I.; Corson, T. W.; Seo, S.-Y. Synthesis of Natural Homoisoflavonoids Having Either 5,7-Dihydroxy-6-methoxy or 7-Hydroxy-5,6-dimethoxy Groups. Molecules (Basel, Switzerland) 2016, 21, 1058. doi:10.3390/molecules21081058
• Dunn, T.; Do, T.; Johnson, N.; Hauser, Q.; Russell, K. C.; Ma, L.
• Choi, K.-Y.; Yang, Y.-H.; Kim, B.-G. Regioselectivity-driven evolution of CYP102D1 for improved synthesis of 3'-ortho-dihydroxyisoflavone. Enzyme and microbial technology 2015, 71, 20–27. doi:10.1016/j.enzmictec.2015.01.004
• Hong, H. J.; Lee, J. I. A Versatile Synthesis of O-Desmethylangolensin Analogues from Methoxy-Substituted Benzoic Acids. Journal of the Korean Chemical Society 2014, 58, 569–574. doi:10.5012/jkcs.2014.58.6.569
• Semeniuchenko, V.; Exner, T. E.; Khilya, V.; Groth, U. Homogeneous hydrogenation of electron-deficient alkenes by iridium complexes. Applied Organometallic Chemistry 2011, 25, 804–809. doi:10.1002/aoc.1841
• Poonam; Kumari, P.; Nagpal, R.; Chauhan, S. M. S. Formation of hydridocobalt(III) phthalocyanine by reaction of cobalt(II) phthalocyanines with sodium borohydride and its reactions with antioxidant isoflavones. New Journal of Chemistry 2011, 35, 2639–2646. doi:10.1039/c1nj20582j
• Pan, C.-H.; Kim, E. S.; Jung, S. H.; Nho, C. W.; Lee, J. K. Tectorigenin inhibits IFN-γ/LPS-induced inflammatory responses in murine macrophage RAW 264.7 cells. Archives of pharmacal research 2008, 31, 1447–1456. doi:10.1007/s12272-001-2129-7
• Chemler, J. A.; Leonard; Koffas, M. A. G. Flavonoid Biotransformations in Microorganisms. Anthocyanins; Springer New York, 2008; pp 191–255. doi:10.1007/978-0-387-77335-3_7
• Won, D.; Shin, B. Synthesis and the Absolute Configurations of Isoflavanone Enantiomers. Journal of Applied Biological Chemistry 2008, 51, 17–19. doi:10.3839/jabc.2008.004
• Won, D.; Shin, B.-K.; Kang, S.-I.; Hur, H.-G.; Kim, M.; Han, J. Absolute configurations of isoflavan-4-ol stereoisomers. Bioorganic & medicinal chemistry letters 2008, 18, 1952–1957. doi:10.1016/j.bmcl.2008.01.116
• Seoud, O. A. E.; Koschella, A.; Fidale, L. C.; Dorn, S.; Heinze, T. Applications of ionic liquids in carbohydrate chemistry: a window of opportunities. Biomacromolecules 2007, 8, 2629–2647. doi:10.1021/bm070062i

Explore citations to this article at