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For: 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]
Number Citing Articles
1 Yue G, Liu Q, Wei J, Pi Y, Qiu D, Mo F. Direct Stannylation and Silylation of Arylmethanols by Palladium Catalysis. J Org Chem 2023;88:2735-41. [PMID: 36790386 DOI: 10.1021/acs.joc.2c02265] [Reference Citation Analysis]
2 Kuchkina N, Sorokina S, Torozova A, Bykov A, Shifrina Z. Ni nanoparticles Entrapped by a Functional Dendrimer as a Highly Efficient and Recyclable Catalyst for Suzuki‐Miyaura Cross‐Coupling Reactions. ChemistrySelect 2022;7. [DOI: 10.1002/slct.202202653] [Reference Citation Analysis]
3 Lalloo N, Brigham CE, Sanford MS. Mechanism-Driven Development of Group 10 Metal-Catalyzed Decarbonylative Coupling Reactions. Acc Chem Res 2022;55:3430-44. [PMID: 36382937 DOI: 10.1021/acs.accounts.2c00496] [Reference Citation Analysis]
4 Kagilev AA, Gafurov ZN, Sakhapov IF, Islamov DR, Kantyukov AO, Mikhailov IK, Yakhvarov DG. Crystal Structure of the Organonickel Sigma Complex [NiBr(Tcpp)(bpy)]. Russ J Gen Chem 2022;92:2659-2665. [DOI: 10.1134/s1070363222120155] [Reference Citation Analysis]
5 Sorokina SA, Kuchkina NV, Ezernitskaya MG, Bykov AV, Vasiliev AL, Efimov NN, Shifrina ZB. Ni Nanoparticles Stabilized by Hyperbranched Polymer: Does the Architecture of the Polymer Affect the Nanoparticle Characteristics and Their Performance in Catalysis? Int J Mol Sci 2022;23. [PMID: 36430353 DOI: 10.3390/ijms232213874] [Reference Citation Analysis]
6 Faddeev NA, Kuriganova AB, Leont’ev IN, Smirnova NV. Palladium-Based Electroactive Materials for Environmental Catalysis. Dokl Phys Chem 2022;507:139-146. [DOI: 10.1134/s0012501622700063] [Reference Citation Analysis]
7 Kelly WJ, Belabassi Y, Gouault‐bironneau S, Montchamp J, Greaves ME. 1,1′‐Bis(diphenylphosphino)ferrocene. Encyclopedia of Reagents for Organic Synthesis 2022. [DOI: 10.1002/047084289x.rb161.pub3] [Reference Citation Analysis]
8 Rostovshchikova TN, Shilina MI, Gurevich SA, Yavsin DA, Veselov GB, Vedyagin AA. New Approaches to the Synthesis of Ultralow-Palladium Automotive Emission Control Catalysts. Dokl Phys Chem 2022;506:123-130. [DOI: 10.1134/s001250162260019x] [Reference Citation Analysis]
9 Schleinitz J, Langevin M, Smail Y, Wehnert B, Grimaud L, Vuilleumier R. Machine Learning Yield Prediction from NiCOlit, a Small-Size Literature Data Set of Nickel Catalyzed C-O Couplings. J Am Chem Soc 2022. [PMID: 35939717 DOI: 10.1021/jacs.2c05302] [Reference Citation Analysis]
10 Bharathi M, Indira S, Vinoth G, Shanmuga Bharathi K. Implanted mixed ligand Ni complex of phenolic Schiff base and 2, 2’ bipyridine on MCM-41 as an efficient catalyst for Suzuki–Miyaura cross-coupling reactions: a greener approach. Res Chem Intermed. [DOI: 10.1007/s11164-022-04786-7] [Reference Citation Analysis]
11 Chernyshev VM, Khazipov OV, Shevchenko MA, Pasyukov DV, Burykina JV, Minyaev ME, Eremin DB, Ananikov VP. Discovery of the N–NHC Coupling Process under the Conditions of Pd/NHC- and Ni/NHC-Catalyzed Buchwald–Hartwig Amination. Organometallics. [DOI: 10.1021/acs.organomet.2c00166] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
12 Giddaerappa, Manjunatha N, Shantharaja, Hojamberdiev M, Sannegowda LK. Nitrogen-rich palladium tetra amino-hippuric acid phthalocyanine complex and its hybrid composite with multi-walled carbon nanotubes for supercapacitor application. Journal of Energy Storage 2022;50:104696. [DOI: 10.1016/j.est.2022.104696] [Reference Citation Analysis]
13 Wu FW, Mao YJ, Pu J, Li HL, Ye P, Xu ZY, Lou SJ, Xu DQ. Ni-catalysed deamidative fluorination of amides with electrophilic fluorinating reagents. Org Biomol Chem 2022;20:4091-5. [PMID: 35522070 DOI: 10.1039/d2ob00519k] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
14 Guo X, Dang H, Wisniewski SR, Simmons EM. Nickel-Catalyzed Suzuki–Miyaura Cross-Coupling Facilitated by a Weak Amine Base with Water as a Cosolvent. Organometallics. [DOI: 10.1021/acs.organomet.2c00197] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
15 Wang K, Jiang H, Liu H, Chen H, Zhang F. Accelerated Direct Hydroxylation of Aryl Chlorides with Water to Phenols via the Proximity Effect in a Heterogeneous Metallaphotocatalyst. ACS Catal . [DOI: 10.1021/acscatal.1c05070] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
16 Kranthikumar R. Recent Advances in C(sp 3 )–C(sp 3 ) Cross-Coupling Chemistry: A Dominant Performance of Nickel Catalysts. Organometallics. [DOI: 10.1021/acs.organomet.2c00032] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
17 Kancherla R, Muralirajan K, Rueping M. Excited-state palladium-catalysed reductive alkylation of imines: scope and mechanism. Chem Sci 2022;13:8583-9. [DOI: 10.1039/d2sc02363f] [Reference Citation Analysis]