Nickel-Catalyzed Carbonylative Synthesis of Functionalized Alkyl Iodides
Functionalized alkyl iodides are important compounds in organic chemistry and biology. In this communication, we developed an interesting nickel-catalyzed carbonylative synthesis of functionalized alkyl iodides from aryl iodides and ethers. With Mo(CO) as the solid CO source, both cyclic and acyclic...
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| Published in | iScience Vol. 8; pp. 175 - 182 |
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| Main Authors | , , , , , |
| Format | Journal Article |
| Language | English |
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United States
Elsevier
26.10.2018
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| Subjects | |
| Online Access | Get full text |
| ISSN | 2589-0042 2589-0042 |
| DOI | 10.1016/j.isci.2018.09.024 |
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| Abstract | Functionalized alkyl iodides are important compounds in organic chemistry and biology. In this communication, we developed an interesting nickel-catalyzed carbonylative synthesis of functionalized alkyl iodides from aryl iodides and ethers. With Mo(CO)
as the solid CO source, both cyclic and acyclic ethers were activated, which is also a challenging topic in organic synthesis. Functionalized alkyl iodides were prepared in moderate to excellent yields with outstanding functional group tolerance. Besides the high value of the obtained products, all the atoms from the starting materials were incorporated in the final products and the reaction had high atom efficiency as well. |
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| AbstractList | Functionalized alkyl iodides are important compounds in organic chemistry and biology. In this communication, we developed an interesting nickel-catalyzed carbonylative synthesis of functionalized alkyl iodides from aryl iodides and ethers. With Mo(CO)6 as the solid CO source, both cyclic and acyclic ethers were activated, which is also a challenging topic in organic synthesis. Functionalized alkyl iodides were prepared in moderate to excellent yields with outstanding functional group tolerance. Besides the high value of the obtained products, all the atoms from the starting materials were incorporated in the final products and the reaction had high atom efficiency as well.
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Nickel-catalyzed carbonylative synthesis of functionalized alkyl iodides
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With Mo(CO)6 as the solid CO source, carbonylative ether activation
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Good yields of functionalized alkyl iodides
Chemistry; Catalysis; Organic Synthesis Functionalized alkyl iodides are important compounds in organic chemistry and biology. In this communication, we developed an interesting nickel-catalyzed carbonylative synthesis of functionalized alkyl iodides from aryl iodides and ethers. With Mo(CO)6 as the solid CO source, both cyclic and acyclic ethers were activated, which is also a challenging topic in organic synthesis. Functionalized alkyl iodides were prepared in moderate to excellent yields with outstanding functional group tolerance. Besides the high value of the obtained products, all the atoms from the starting materials were incorporated in the final products and the reaction had high atom efficiency as well.Functionalized alkyl iodides are important compounds in organic chemistry and biology. In this communication, we developed an interesting nickel-catalyzed carbonylative synthesis of functionalized alkyl iodides from aryl iodides and ethers. With Mo(CO)6 as the solid CO source, both cyclic and acyclic ethers were activated, which is also a challenging topic in organic synthesis. Functionalized alkyl iodides were prepared in moderate to excellent yields with outstanding functional group tolerance. Besides the high value of the obtained products, all the atoms from the starting materials were incorporated in the final products and the reaction had high atom efficiency as well. Functionalized alkyl iodides are important compounds in organic chemistry and biology. In this communication, we developed an interesting nickel-catalyzed carbonylative synthesis of functionalized alkyl iodides from aryl iodides and ethers. With Mo(CO) as the solid CO source, both cyclic and acyclic ethers were activated, which is also a challenging topic in organic synthesis. Functionalized alkyl iodides were prepared in moderate to excellent yields with outstanding functional group tolerance. Besides the high value of the obtained products, all the atoms from the starting materials were incorporated in the final products and the reaction had high atom efficiency as well. Functionalized alkyl iodides are important compounds in organic chemistry and biology. In this communication, we developed an interesting nickel-catalyzed carbonylative synthesis of functionalized alkyl iodides from aryl iodides and ethers. With Mo(CO)6 as the solid CO source, both cyclic and acyclic ethers were activated, which is also a challenging topic in organic synthesis. Functionalized alkyl iodides were prepared in moderate to excellent yields with outstanding functional group tolerance. Besides the high value of the obtained products, all the atoms from the starting materials were incorporated in the final products and the reaction had high atom efficiency as well. : Chemistry; Catalysis; Organic Synthesis Subject Areas: Chemistry, Catalysis, Organic Synthesis |
| Author | Qi, Xinxin Ying, Jun Wu, Xiao-Feng Xu, Cong Wu, Fu-Peng Peng, Jin-Bao |
| AuthorAffiliation | 1 Department of Chemistry, Zhejiang Sci-Tech University, Hangzhou, Zhejiang 310018, People's Republic of China 2 Leibniz-Institut für Katalyse e.V. an der Universität Rostock, Albert-Einstein-Straße 29a, Rostock 18059, Germany |
| AuthorAffiliation_xml | – name: 1 Department of Chemistry, Zhejiang Sci-Tech University, Hangzhou, Zhejiang 310018, People's Republic of China – name: 2 Leibniz-Institut für Katalyse e.V. an der Universität Rostock, Albert-Einstein-Straße 29a, Rostock 18059, Germany |
| Author_xml | – sequence: 1 givenname: Jin-Bao surname: Peng fullname: Peng, Jin-Bao – sequence: 2 givenname: Fu-Peng surname: Wu fullname: Wu, Fu-Peng – sequence: 3 givenname: Cong surname: Xu fullname: Xu, Cong – sequence: 4 givenname: Xinxin surname: Qi fullname: Qi, Xinxin – sequence: 5 givenname: Jun surname: Ying fullname: Ying, Jun – sequence: 6 givenname: Xiao-Feng orcidid: 0000-0001-6622-3328 surname: Wu fullname: Wu, Xiao-Feng |
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| Cites_doi | 10.1039/C6RA18388C 10.1002/anie.200301736 10.1021/acs.joc.7b02457 10.1039/c39890001253 10.1021/ja4098093 10.1038/nature00908 10.1021/acscatal.7b01436 10.1002/cctc.201700517 10.1002/anie.201709807 10.1021/acs.orglett.7b01481 10.1246/bcsj.67.879 10.1021/acs.orglett.7b02139 10.1039/C7CC01159H 10.1002/ejoc.201200794 10.1021/ja00132a009 10.1016/j.tet.2014.05.026 10.1016/j.jorganchem.2006.01.010 10.1021/jm9505526 10.1002/chem.201403093 10.1039/C6SC04371B 10.1021/jacs.6b02314 10.1021/ja048946m 10.1038/nchem.2903 10.1002/anie.197707891 |
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| References | Liu (10.1016/j.isci.2018.09.024_bib10) 2014; 20 Didiuk (10.1016/j.isci.2018.09.024_bib3) 1995; 117 Gabriele (10.1016/j.isci.2018.09.024_bib5) 2012; 2012 Watanabe (10.1016/j.isci.2018.09.024_bib23) 1994; 67 Torres (10.1016/j.isci.2018.09.024_bib20) 2016; 138 Lübcke (10.1016/j.isci.2018.09.024_bib11) 2017; 19 Getzler (10.1016/j.isci.2018.09.024_bib6) 2004; 126 Peng (10.1016/j.isci.2018.09.024_bib16) 2017; 28 Jones (10.1016/j.isci.2018.09.024_bib7) 2017; 19 Peng (10.1016/j.isci.2018.09.024_bib15) 2018; 57 Christensen (10.1016/j.isci.2018.09.024_bib1) 2014; 70 Seki (10.1016/j.isci.2018.09.024_bib18) 1977; 16 Tsuji (10.1016/j.isci.2018.09.024_bib22) 1989 Tjutrins (10.1016/j.isci.2018.09.024_bib19) 2016; 8 Wu (10.1016/j.isci.2018.09.024_bib25) 2017; 9 Ohshita (10.1016/j.isci.2018.09.024_bib14) 2006; 691 Trewick (10.1016/j.isci.2018.09.024_bib21) 2002; 419 DeGraw (10.1016/j.isci.2018.09.024_bib2) 1997; 40 Quesnel (10.1016/j.isci.2018.09.024_bib17) 2013; 135 Kumbhalkar (10.1016/j.isci.2018.09.024_bib9) 2017; 7 Kinney (10.1016/j.isci.2018.09.024_bib8) 2018; 10 Mukherjee (10.1016/j.isci.2018.09.024_bib13) 2017; 53 Frei (10.1016/j.isci.2018.09.024_bib4) 2018; 83 Wu (10.1016/j.isci.2018.09.024_bib24) 2016; 6 Wuts (10.1016/j.isci.2018.09.024_bib26) 2014 Morimoto (10.1016/j.isci.2018.09.024_bib12) 2004; 43 |
| References_xml | – volume: 6 start-page: 83831 year: 2016 ident: 10.1016/j.isci.2018.09.024_bib24 article-title: Palladium-catalyzed carbonylative transformation of aryl chlorides and aryl tosylates publication-title: RSC Adv. doi: 10.1039/C6RA18388C – volume: 43 start-page: 5580 year: 2004 ident: 10.1016/j.isci.2018.09.024_bib12 article-title: Evolution of carbonylation catalysis: no need for carbon monoxide publication-title: Angew. Chem. Int. Ed. doi: 10.1002/anie.200301736 – volume: 83 start-page: 1510 year: 2018 ident: 10.1016/j.isci.2018.09.024_bib4 article-title: Regioselective reaction of heterocyclic N-oxides, an acyl chloride, and cyclic thioethers publication-title: J. Org. Chem. doi: 10.1021/acs.joc.7b02457 – volume: 28 start-page: 175 year: 2017 ident: 10.1016/j.isci.2018.09.024_bib16 article-title: Recent achievements in carbonylation reactions: a personal account publication-title: Synlett – start-page: 1253 year: 1989 ident: 10.1016/j.isci.2018.09.024_bib22 article-title: Cobalt catalysed ring-opening carbonylation of cyclic ethers using N-(trimethylsilyl)amines publication-title: J. Chem. Soc. Chem. Commun. doi: 10.1039/c39890001253 – volume: 135 start-page: 16841 year: 2013 ident: 10.1016/j.isci.2018.09.024_bib17 article-title: A palladium-catalyzed carbonylation approach to acid chloride synthesis publication-title: J. Am. Chem. Soc. doi: 10.1021/ja4098093 – volume: 419 start-page: 174 year: 2002 ident: 10.1016/j.isci.2018.09.024_bib21 article-title: Oxidative demethylation by Escherichia coli AlkB directly reverts DNA base damage publication-title: Nature doi: 10.1038/nature00908 – volume: 7 start-page: 5248 year: 2017 ident: 10.1016/j.isci.2018.09.024_bib9 article-title: Ring opening of biomass-derived cyclic ethers to dienes over silica/alumina publication-title: ACS Catal. doi: 10.1021/acscatal.7b01436 – volume: 9 start-page: 3121 year: 2017 ident: 10.1016/j.isci.2018.09.024_bib25 article-title: Palladium-catalyzed ligand-controlled selective synthesis of aldehydes and acids from aryl halides and formic acid publication-title: ChemCatChem doi: 10.1002/cctc.201700517 – volume: 57 start-page: 1152 year: 2018 ident: 10.1016/j.isci.2018.09.024_bib15 article-title: Ligand- and solvent-controlled regio- and chemodivergent carbonylative reactions publication-title: Angew. Chem. Int. Ed. doi: 10.1002/anie.201709807 – volume: 19 start-page: 3512 year: 2017 ident: 10.1016/j.isci.2018.09.024_bib7 article-title: Regioselective three-component reaction of pyridine N-oxides, acyl chlorides, and cyclic ethers publication-title: Org. Lett. doi: 10.1021/acs.orglett.7b01481 – volume: 67 start-page: 879 year: 1994 ident: 10.1016/j.isci.2018.09.024_bib23 article-title: Co2(CO)8-catalyzed ring-opening carbonylation of cyclic ethers using N-silylamines publication-title: Bull. Chem. Soc. Jpn. doi: 10.1246/bcsj.67.879 – volume: 19 start-page: 4548 year: 2017 ident: 10.1016/j.isci.2018.09.024_bib11 article-title: Trifluoromethylthiolation-based bifunctionalization of diazocarbonyl compounds by rhodium catalysis publication-title: Org. Lett. doi: 10.1021/acs.orglett.7b02139 – volume: 53 start-page: 3493 year: 2017 ident: 10.1016/j.isci.2018.09.024_bib13 article-title: Ring-opening of cyclic ethers by aluminum hydridotriphenylborate publication-title: Chem. Commun. (Camb.) doi: 10.1039/C7CC01159H – volume: 2012 start-page: 6825 year: 2012 ident: 10.1016/j.isci.2018.09.024_bib5 article-title: Oxidative carbonylation as a powerful tool for the direct synthesis of carbonylated heterocycles publication-title: Eur. J. Org. Chem. doi: 10.1002/ejoc.201200794 – volume: 117 start-page: 7097 year: 1995 ident: 10.1016/j.isci.2018.09.024_bib3 article-title: Enantio-, diastereo-, and regioselective zirconium-catalyzed carbomagnesation of cyclic ethers with higher alkyls of magnesium. utility in synthesis and mechanistic implications publication-title: J. Am. Chem. Soc. doi: 10.1021/ja00132a009 – volume: 70 start-page: 4942 year: 2014 ident: 10.1016/j.isci.2018.09.024_bib1 article-title: Ring-opening of cyclic ethers with carbon–carbon bond formation by Grignard reagents publication-title: Tetrahedron doi: 10.1016/j.tet.2014.05.026 – volume: 691 start-page: 1907 year: 2006 ident: 10.1016/j.isci.2018.09.024_bib14 article-title: Ring-opening reactions of cyclic ethers with diiodo- and dibromodimethylsilane equivalents publication-title: J. Organomet. Chem. doi: 10.1016/j.jorganchem.2006.01.010 – volume: 40 start-page: 370 year: 1997 ident: 10.1016/j.isci.2018.09.024_bib2 article-title: Analogues of methotrexate in rheumatoid arthritis. 1. effects of 10-deazaaminopterin analogues on type II collagen-induced arthritis in mice publication-title: J. Med. Chem. doi: 10.1021/jm9505526 – volume: 20 start-page: 8308 year: 2014 ident: 10.1016/j.isci.2018.09.024_bib10 article-title: Palladium-catalyzed intramolecular reductive cross-coupling of Csp2-Csp3 bond formation publication-title: Chem. Eur. J. doi: 10.1002/chem.201403093 – volume: 8 start-page: 1002 year: 2016 ident: 10.1016/j.isci.2018.09.024_bib19 article-title: A palladium-catalyzed synthesis of (hetero)aryl-substituted imidazoles from aryl halides, imines and carbon monoxide publication-title: Chem. Sci. doi: 10.1039/C6SC04371B – volume: 138 start-page: 7315 year: 2016 ident: 10.1016/j.isci.2018.09.024_bib20 article-title: From aryl iodides to 1,3-dipoles: design and mechanism of a palladium catalyzed multicomponent synthesis of pyrroles publication-title: J. Am. Chem. Soc. doi: 10.1021/jacs.6b02314 – volume: 126 start-page: 6842 year: 2004 ident: 10.1016/j.isci.2018.09.024_bib6 article-title: Catalytic carbonylation of β-lactones to succinic anhydrides publication-title: J. Am. Chem. Soc. doi: 10.1021/ja048946m – volume: 10 start-page: 193 year: 2018 ident: 10.1016/j.isci.2018.09.024_bib8 article-title: A general approach to intermolecular carbonylation of arene C-H bonds to ketones through catalytic aroyl triflate formation publication-title: Nat. Chem. doi: 10.1038/nchem.2903 – volume: 16 start-page: 789 year: 1977 ident: 10.1016/j.isci.2018.09.024_bib18 article-title: Co2(CO)8 catalyzed reactions of cyclic ethers with hydrosilanes and carbon monoxide publication-title: Angew. Chem. Int. Ed. doi: 10.1002/anie.197707891 – year: 2014 ident: 10.1016/j.isci.2018.09.024_bib26 |
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