SmI₂-mediated dimerization of indolylbutenones and synthesis of the myxobacterial natural product indiacen B

Scholarly Works

• Vidari, G.; Chiodi, D.; Porta, A.; Zanoni, G. doi:10.1002/0471264180.or115.02
• Karuna, C.; Reddy, C. V. R.; Laxminarayana, E. A Facile Synthesis of 1-(4-Methoxybenzyl)-4-[(E)-4-(trimethylsilyl)but-1-en-3-yn-1-yl]-1H-indole and 2-Aryl-1-(4-methoxybenzyl)-1H-indole-4-carbaldehydes. Russian Journal of Organic Chemistry 2022, 58, 1516–1519. doi:10.1134/s1070428022100190
• Bailly, C. A world tour in the name of natural products. Phytomedicine : international journal of phytotherapy and phytopharmacology 2022, 100, 154080. doi:10.1016/j.phymed.2022.154080
• Heravi, M. M.; Amiri, Z.; Kafshdarzadeh, K.; Zadsirjan, V. Synthesis of indole derivatives as prevalent moieties present in selected alkaloids. RSC advances 2021, 11, 33540–33612. doi:10.1039/d1ra05972f
• Bhat, M. A.; Mishra, A. K.; Bhat, M. A.; Banday, M. I.; Bashir, O.; Rather, I. A.; Rahman, S.; Shah, A. A.; Jan, A. T. Myxobacteria as a Source of New Bioactive Compounds: A Perspective Study. Pharmaceutics 2021, 13, 1265. doi:10.3390/pharmaceutics13081265
• Justaud, F.; Hachem, A.; Grée, R. Recent Developments in the Meyer‐Schuster Rearrangement. European Journal of Organic Chemistry 2021, 2021, 514–542. doi:10.1002/ejoc.202001494
• Liu, C.; Yan, Q.; Yongjun, L. Recent Development of Samarium Diiodide and Other Samarium Reagents in Organic Transformation. Chinese Journal of Organic Chemistry 2021, 41, 2202. doi:10.6023/cjoc202011034
• Trushkov, I. V.; Uchuskin, M. G.; Abaev, V. T.; Serdyuk, O. V. Indolylvinyl Ketones: Building Blocks for the Synthesis of Natural Products and Bioactive Compounds. Synthesis 2019, 51, 787–815. doi:10.1055/s-0037-1611702
• Dehhaghi, M.; Mohammadipanah, F.; Guillemin, G. J. Myxobacterial natural products: An under-valued source of products for drug discovery for neurological disorders. Neurotoxicology 2018, 66, 195–203. doi:10.1016/j.neuro.2018.02.017
• Nguyen, T. T.; Koh, M. J.; Mann, T. J.; Schrock, R. R.; Hoveyda, A. H. Synthesis of E- and Z-trisubstituted alkenes by catalytic cross-metathesis. Nature 2017, 552, 347–354. doi:10.1038/nature25002
• Borowiecki, P.; Justyniak, I.; Ochal, Z. Lipase-catalyzed kinetic resolution approach toward enantiomerically enriched 1-(β-hydroxypropyl)indoles. Tetrahedron: Asymmetry 2017, 28, 1717–1732. doi:10.1016/j.tetasy.2017.10.010
• Borowiecki, P.; Dranka, M.; Ochal, Z. Lipase-Catalyzed Kinetic Resolution of N-Substituted 1-(β-Hydroxypropyl)indoles by Enantioselective Acetylation. European Journal of Organic Chemistry 2017, 2017, 5378–5390. doi:10.1002/ejoc.201700889
• Anantoju, K. K.; Mohd., B. S.; Maringanti, T. C. An efficient and concise synthesis of Indiacen A and Indiacen B. Tetrahedron Letters 2017, 58, 1499–1500. doi:10.1016/j.tetlet.2017.03.002
• Herrmann, J.; Fayad, A. A.; Müller, R. Natural products from myxobacteria: novel metabolites and bioactivities. Natural product reports 2016, 34, 135–160. doi:10.1039/c6np00106h
• Marsch, N.; Kock, M.; Lindel, T. Study on the synthesis of the cyclopenta[f]indole core of raputindole A. Beilstein journal of organic chemistry 2016, 12, 334–342. doi:10.3762/bjoc.12.36

Explore citations to this article at