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For: Rayadurgam J, Sana S, Sasikumar M, Gu Q. Palladium catalyzed C–C and C–N bond forming reactions: an update on the synthesis of pharmaceuticals from 2015–2020. Org Chem Front 2021;8:384-414. [DOI: 10.1039/d0qo01146k] [Cited by in Crossref: 36] [Cited by in F6Publishing: 38] [Article Influence: 18.0] [Reference Citation Analysis]
Number Citing Articles
1 Gholinejad M, Khosravi F, Sansano JM, Vishnuraj R, Pullithadathil B. Bimetallic AuNi Nanoparticles Supported on Mesoporous MgO as Catalyst for Sonogashira-Hagihara Cross-Coupling Reaction. Journal of Organometallic Chemistry 2023. [DOI: 10.1016/j.jorganchem.2023.122636] [Reference Citation Analysis]
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5 Pei M, Luo X, Tang Q, Huang N, Wang L. The application research on Cu-Al@SBA-15 bimetallic synergistic effect in the C-X bond sequential assembly. Catalysis Communications 2022;172:106548. [DOI: 10.1016/j.catcom.2022.106548] [Reference Citation Analysis]
6 Mahato SK, Zhang T, Chatani N. Ir(III)-Catalyzed C(sp2)–H Amidation of 2-Aroylimidazoles with 2,2,2-Trichloroethoxycarbonyl Azide (TrocN3). J Org Chem 2022. [DOI: 10.1021/acs.joc.2c02056] [Reference Citation Analysis]
7 Miao X, Hu Y, Liu F, Sun Y, Sun D, Wu A, Zhu Y. Synthesis of Diversified Pyrazolo[3,4-b]pyridine Frameworks from 5-Aminopyrazoles and Alkynyl Aldehydes via Switchable C≡C Bond Activation Approaches. Molecules 2022;27:6381. [DOI: 10.3390/molecules27196381] [Reference Citation Analysis]
8 Arora A, Oswal P, Sharma D, Tyagi A, Purohit S, Sharma P, Kumar A. Molecular Organosulphur, Organoselenium and Organotellurium Complexes as Homogeneous Transition Metal Catalytic Systems for Suzuki Coupling. ChemistrySelect 2022;7. [DOI: 10.1002/slct.202201704] [Reference Citation Analysis]
9 Buğday N, Khan S, Yaşar S, Bulut F, Boulebd H, Karabıyık H, Karabıyık H, Öz E, Rehman AU, Özdemir İ. Pd-NHC complex catalyzed C-H bond activation reactions of caffeine and 2-isobuthylthiazole. Molecular Catalysis 2022;530:112590. [DOI: 10.1016/j.mcat.2022.112590] [Reference Citation Analysis]
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12 Tessema E, Fan Y, Chiu C, Elakkat V, Rahayu HA, Shen C, Shanthakumar KC, Zhang P, Lu N. Recoverable low fluorine content palladium complex-catalyzed Suzuki-Miyaura and Sonogashira coupling reactions under thermomorphic mode. Tetrahedron 2022. [DOI: 10.1016/j.tet.2022.132961] [Reference Citation Analysis]
13 Khalilzadeh MA, Kim SY, Jang HW, Luque R, Varma RS, Venditti RA, Shokouhimehr M. Carbohydrate-based nanostructured catalysts: applications in organic transformations. Materials Today Chemistry 2022;24:100869. [DOI: 10.1016/j.mtchem.2022.100869] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
14 Sundarraman B, Rengan R, Semeril D. NNO Pincer Ligand-Supported Palladium(II) Complexes: Direct Synthesis of Quinazolines via Acceptorless Double Dehydrogenative Coupling of Alcohols. Organometallics. [DOI: 10.1021/acs.organomet.2c00062] [Cited by in Crossref: 1] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
15 Anusha G, Indira M, Kumar IS, Sarma LS, Reddy KR, Govardhana Reddy PV, Aminabhavi TM. Synthesis of bis-1,3-(benz)azoles catalyzed by palladium-PEPPSI complex-based catalysts and the study of photophysical properties. Chemosphere 2022;:134751. [PMID: 35490757 DOI: 10.1016/j.chemosphere.2022.134751] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
16 Dow NW, Pedersen PS, Chen TQ, Blakemore DC, Dechert-Schmitt AM, Knauber T, MacMillan DWC. Decarboxylative Borylation and Cross-Coupling of (Hetero)aryl Acids Enabled by Copper Charge Transfer Catalysis. J Am Chem Soc 2022;144:6163-72. [PMID: 35377627 DOI: 10.1021/jacs.2c01630] [Cited by in Crossref: 7] [Cited by in F6Publishing: 10] [Article Influence: 7.0] [Reference Citation Analysis]
17 Singh A, Kumar M, Bhalla V. Phenazine‐based supramolecular photosensitizing assemblies: A “smart” selectivity control on catalytic activity of Pd(II) nanoparticles. Aggregate. [DOI: 10.1002/agt2.192] [Reference Citation Analysis]
18 Tse MH, Zhong R, Kwong FY. Palladium-Catalyzed Miyaura Borylation of Overly Crowded Aryl Chlorides Enabled by a Complementary Localized/Remote Steric Bulk of Ligand Chassis. ACS Catal 2022;12:3507-15. [DOI: 10.1021/acscatal.2c00263] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
19 Ng SS, Chen Z, Yuen OY, So CM. An indole-amide-based phosphine ligand enabling a general palladium-catalyzed sterically hindered Suzuki-Miyaura cross-coupling reaction. Org Biomol Chem 2022;20:1373-8. [PMID: 35080549 DOI: 10.1039/d1ob02294f] [Reference Citation Analysis]
20 Xu Z, Xu J, Zheng W, Li Y. Palladium supported on ethylenediaminetetraacetic acid functionalized cellulose: synthesis, characterization, and its application in carbon–carbon cross-coupling reactions. Cellulose. [DOI: 10.1007/s10570-022-04459-z] [Reference Citation Analysis]
21 Kinzhalov MA, Luzyanin KV. Synthesis and Contemporary Applications of Platinum Group Metals Complexes with Acyclic Diaminocarbene Ligands (Review). Russ J Inorg Chem 2022;67:48-90. [DOI: 10.1134/s0036023622010065] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
22 Anju PJ, Neetha M, Anilkumar G. Recent Advances on N‐Heterocyclic Carbene‐Palladium‐catalyzed Heck Reaction. ChemistrySelect 2022;7. [DOI: 10.1002/slct.202103564] [Reference Citation Analysis]
23 Ojha S, Panda N. Pd-Catalyzed desulfitative arylation of olefins by N-methoxysulfonamide. Org Biomol Chem 2022. [PMID: 35073396 DOI: 10.1039/d1ob02360h] [Reference Citation Analysis]
24 Chernyshev VM, Ananikov VP. Nickel and Palladium Catalysis: Stronger Demand than Ever. ACS Catal 2022;12:1180-200. [DOI: 10.1021/acscatal.1c04705] [Cited by in Crossref: 13] [Cited by in F6Publishing: 13] [Article Influence: 13.0] [Reference Citation Analysis]
25 Govada GV, Sabbasani RR. A new outlook in oxidative transformations and coupling reactions via in situ generation of organic chloramines. Applied Organom Chemis. [DOI: 10.1002/aoc.6518] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
26 Jin T, Xu L, Wang P, Hu X, Zhang R, Wu Z, Du W, Kan W, Li K, Wang C, Zhou Y, Li J, Liu T. Discovery and Development of a Potent, Selective, and Orally Bioavailable CHK1 Inhibitor Candidate: 5-((4-((3-Amino-3-methylbutyl)amino)-5-(trifluoromethyl)pyrimidin-2-yl)amino)picolinonitrile. J Med Chem 2021;64:15069-90. [PMID: 34665631 DOI: 10.1021/acs.jmedchem.1c00994] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
27 Hughes DL. Review of Synthetic Routes and Crystalline Forms of the Oncology Drugs Capmatinib, Selpercatinib, and Pralsetinib. Org Process Res Dev 2021;25:2192-2204. [DOI: 10.1021/acs.oprd.1c00282] [Reference Citation Analysis]
28 Pan P, Chen L, Zhang X, Yan M. Diverse functionalization of aryl halides mediated by bis(phenylsulfonyl)methane. Tetrahedron 2021;96:132371. [DOI: 10.1016/j.tet.2021.132371] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
29 Martinez EE, Moreno MR, Barksdale CA, Michaelis DJ. Effect of Precatalyst Oxidation State in C–N Cross-Couplings with 2-Phosphinoimidazole-Derived Bimetallic Pd(I) and Pd(II) Complexes. Organometallics 2021;40:2763-7. [DOI: 10.1021/acs.organomet.1c00315] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
30 Elmekawy A. Simultaneous Determination of Residual Palladium and Thiol Homogeneous Scavenger N-Acetylcysteine in Active Pharmaceutical Ingredients Using Inductive Coupled Plasma-Mass Spectrometry. Org Process Res Dev 2021;25:1352-1359. [DOI: 10.1021/acs.oprd.0c00542] [Reference Citation Analysis]
31 Oswal P, Arora A, Gairola S, Datta A, Kumar A. Organosulfur, organoselenium, and organotellurium ligands in the development of palladium, nickel, and copper-based catalytic systems for Heck coupling. New J Chem 2021;45:21449-87. [DOI: 10.1039/d1nj02971a] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 3.5] [Reference Citation Analysis]