Transition-metal-catalyzed C–C bond macrocyclization via intramolecular C–H bond activation
Macrocycles are commonly synthesized via late-stage macrolactamization and macrolactonization. Strategies involving C–C bond macrocyclization have been reported, and examples include the transition-metal-catalyzed ring-closing metathesis and coupling reactions. In this mini-review, we summarize the...
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sg-ntu-dr.10356-1688422023-06-23T15:32:02Z Transition-metal-catalyzed C–C bond macrocyclization via intramolecular C–H bond activation Wang, Xiao. Lu, Ming-Zhu Loh, Teck-Peng School of Chemistry, Chemical Engineering and Biotechnology Science::Chemistry Transition-Metal Catalysis Macrocyclization Macrocycles are commonly synthesized via late-stage macrolactamization and macrolactonization. Strategies involving C–C bond macrocyclization have been reported, and examples include the transition-metal-catalyzed ring-closing metathesis and coupling reactions. In this mini-review, we summarize the recent progress in the direct synthesis of polyketide and polypeptide macrocycles using a transition-metal-catalyzed C–H bond activation strategy. In the first part, rhodium-catalyzed alkene–alkene ring-closing coupling for polyketide synthesis is described. The second part summarizes the synthesis of polypeptide macrocycles. The activation of indolyl and aryl C(sp2)–H bonds followed by coupling with various coupling partners such as aryl halides, arylates, and alkynyl bromide is then documented. Moreover, transition-metal-catalyzed C–C bond macrocyclization reactions via alkyl C(sp3)–H bond activation are also included. We hope that this mini-review will inspire more researchers to explore new and broadly applicable strategies for C–C bond macrocyclization via intramolecular C–H activation. Agency for Science, Technology and Research (A*STAR) Ministry of Education (MOE) Published version We gratefully acknowledge the financial support from the National Natural Science Foundation of China (no. 22101095) and the “Innovation and Entrepreneurship Talents Plan” of Jiangsu Province (M.-Z. Lu). We also acknowledge the financial support from the Distinguished University Professor grant (Nanyang Technological University); the AcRF Tier 1 grants from the Ministry of Education of Singapore (RG11/20 and RT14/20); and the Agency for Science, Technology, and Research (A*STAR) under its MTC Individual Research Grants (M21K2c0114). 2023-06-20T04:55:30Z 2023-06-20T04:55:30Z 2023 Journal Article Wang, X., Lu, M. & Loh, T. (2023). Transition-metal-catalyzed C–C bond macrocyclization via intramolecular C–H bond activation. Catalysts, 13(2), 438-. https://dx.doi.org/10.3390/catal13020438 2073-4344 https://hdl.handle.net/10356/168842 10.3390/catal13020438 2-s2.0-85148934699 2 13 438 en RG11/20 RT14/20 M21K2c0114 Catalysts © 2023 by the authors.Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). application/pdf |
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Science::Chemistry Transition-Metal Catalysis Macrocyclization Wang, Xiao. Lu, Ming-Zhu Loh, Teck-Peng Transition-metal-catalyzed C–C bond macrocyclization via intramolecular C–H bond activation |
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Macrocycles are commonly synthesized via late-stage macrolactamization and macrolactonization. Strategies involving C–C bond macrocyclization have been reported, and examples include the transition-metal-catalyzed ring-closing metathesis and coupling reactions. In this mini-review, we summarize the recent progress in the direct synthesis of polyketide and polypeptide macrocycles using a transition-metal-catalyzed C–H bond activation strategy. In the first part, rhodium-catalyzed alkene–alkene ring-closing coupling for polyketide synthesis is described. The second part summarizes the synthesis of polypeptide macrocycles. The activation of indolyl and aryl C(sp2)–H bonds followed by coupling with various coupling partners such as aryl halides, arylates, and alkynyl bromide is then documented. Moreover, transition-metal-catalyzed C–C bond macrocyclization reactions via alkyl C(sp3)–H bond activation are also included. We hope that this mini-review will inspire more researchers to explore new and broadly applicable strategies for C–C bond macrocyclization via intramolecular C–H activation. |
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School of Chemistry, Chemical Engineering and Biotechnology |
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School of Chemistry, Chemical Engineering and Biotechnology Wang, Xiao. Lu, Ming-Zhu Loh, Teck-Peng |
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Article |
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Wang, Xiao. Lu, Ming-Zhu Loh, Teck-Peng |
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Wang, Xiao. |
title |
Transition-metal-catalyzed C–C bond macrocyclization via intramolecular C–H bond activation |
title_short |
Transition-metal-catalyzed C–C bond macrocyclization via intramolecular C–H bond activation |
title_full |
Transition-metal-catalyzed C–C bond macrocyclization via intramolecular C–H bond activation |
title_fullStr |
Transition-metal-catalyzed C–C bond macrocyclization via intramolecular C–H bond activation |
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Transition-metal-catalyzed C–C bond macrocyclization via intramolecular C–H bond activation |
title_sort |
transition-metal-catalyzed c–c bond macrocyclization via intramolecular c–h bond activation |
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2023 |
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https://hdl.handle.net/10356/168842 |
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