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Liu N, Wu X, Qu J, Chen Y. Nickel-Catalyzed Aminocarbonylation of Aryl Iodides with 1 atm CO. Chem Asian J 2023;18:e202201061. [PMID: 36373896 DOI: 10.1002/asia.202201061] [Reference Citation Analysis]
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Picard B, Fukuyama T, Ryu I. Phosphine-Free Aminocarbonylation Using Pd/DBU Catalyst: Carbonylative Coupling of Aryl Iodides and Amines. J Org Chem 2022. [DOI: 10.1021/acs.joc.2c02369] [Reference Citation Analysis]
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| 3 |
Wang C, Wu X, Li H, Qu J, Chen Y. Carbonylative Cross‐Coupling Reaction of Allylic Alcohols and Organoalanes with 1 atm CO Enabled by Nickel Catalysis. Angew Chem Int Ed 2022;61. [DOI: 10.1002/anie.202210484] [Reference Citation Analysis]
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Kang Y, Lu JL, Zhang Z, Liang YK, Ma AJ, Peng JB. Palladium-Catalyzed Intramolecular Heck/Aminocarbonylation of Alkene-Tethered Iodobenzenes with Nitro Compounds: Synthesis of Carbamoyl-Substituted Benzoheterocycles. J Org Chem 2022. [PMID: 35877191 DOI: 10.1021/acs.joc.2c01253] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
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Huo YW, Qi X, Wu XF. Nickel-Catalyzed Carbonylative Synthesis of α,β-Unsaturated Thioesters from Vinyl Triflates and Arylsulfonyl Chlorides. Org Lett 2022. [PMID: 35613710 DOI: 10.1021/acs.orglett.2c01430] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
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| 6 |
Liu N, Wu X, Wang C, Qu J, Chen Y. Nickel-catalyzed alkoxycarbonylation of aryl iodides with 1 atm CO. Chem Commun (Camb) 2022;58:4643-6. [PMID: 35311870 DOI: 10.1039/d2cc00876a] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 6.0] [Reference Citation Analysis]
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| 7 |
Hou L, Huang W, Wu X, Qu J, Chen Y. Nickel-Catalyzed Carbonylation of Cyclopropanol with Benzyl Bromide for Multisubstituted Cyclopentenone Synthesis. Org Lett 2022. [PMID: 35389666 DOI: 10.1021/acs.orglett.2c00798] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 5.0] [Reference Citation Analysis]
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| 8 |
Xu RR, Wen D, Qi X, Wu XF. Palladium-catalyzed cascade Heck-type cyclization and reductive aminocarbonylation for the synthesis of functionalized amides. Org Biomol Chem 2022;20:2605-8. [PMID: 35293928 DOI: 10.1039/d2ob00299j] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
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Feng Z, Ma J, Cheung CW. Ni-Catalysed intramolecular reductive aminocarbonylation of 2-haloaryl-tethered nitroarenes for the synthesis of dibenzazepine-based heterocycles. Org Chem Front . [DOI: 10.1039/d2qo00699e] [Reference Citation Analysis]
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| 10 |
Picard B, Fukuyama T, Bando T, Hyodo M, Ryu I. Electron-Catalyzed Aminocarbonylation: Synthesis of α,β-Unsaturated Amides from Alkenyl Iodides, CO, and Amines. Org Lett 2021;23:9505-9. [PMID: 34844411 DOI: 10.1021/acs.orglett.1c03714] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
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