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For: Ismael A, Skrydstrup T, Bayer A. Carbonylative Suzuki-Miyaura couplings of sterically hindered aryl halides: synthesis of 2-aroylbenzoate derivatives. Org Biomol Chem 2020;18:1754-9. [PMID: 32065204 DOI: 10.1039/d0ob00044b] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 3.5] [Reference Citation Analysis]
Number Citing Articles
1 Horbaczewskyj CS, Fairlamb IJS. Pd-Catalyzed Cross-Couplings: On the Importance of the Catalyst Quantity Descriptors, mol % and ppm. Org Process Res Dev . [DOI: 10.1021/acs.oprd.2c00051] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
2 Neumann KT, Ravn AK, Johansen MB, Donslund AS, Rønne MH, Gudmundsson HG, Skrydstrup T. Reduction of CO 2 to CO and Their Applications. The Chemical Transformations of C1 Compounds 2022. [DOI: 10.1002/9783527831883.ch24] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
3 Xu T, Wang Q, Yang Z, Yi L, Wang JS, Lu W, Ying J, Wu XF. Supported Palladium-Catalyzed Carbonylative Synthesis of Diaryl Ketones from Aryl Bromides and Arylboronic Acids. Chem Asian J 2021;16:2027-30. [PMID: 34107162 DOI: 10.1002/asia.202100540] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 5.0] [Reference Citation Analysis]
4 Loureiro DRP, Soares JX, Maia A, Silva AMN, Rangel M, Azevedo CMG, Hansen SV, Ulven T, Pinto MMM, Reis S, Afonso CMM. One‐Pot Synthesis of Xanthone by Carbonylative Suzuki Coupling Reaction. ChemistrySelect 2021;6:4511-4514. [DOI: 10.1002/slct.202101394] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
5 Etemadi-davan E, Khalili D, Banazadeh AR, Sadri G, Arshad P. Palladium nanoparticles on amino-modified silica-catalyzed C–C bond formation with carbonyl insertion. J IRAN CHEM SOC 2021. [DOI: 10.1007/s13738-021-02171-6] [Reference Citation Analysis]
6 Ismael A, Gevorgyan A, Skrydstrup T, Bayer A. Renewable Solvents for Palladium-Catalyzed Carbonylation Reactions. Org Process Res Dev 2020;24:2665-75. [DOI: 10.1021/acs.oprd.0c00325] [Cited by in Crossref: 14] [Cited by in F6Publishing: 14] [Article Influence: 7.0] [Reference Citation Analysis]
7 Xu J, Zhao F, Wu X. NHC ligand-powered palladium-catalyzed carbonylative C–S bond cleavage of vinyl sulfides: efficient access to tert-butyl arylacrylates. Org Biomol Chem 2020;18:9796-9799. [DOI: 10.1039/d0ob02043e] [Reference Citation Analysis]