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For: Devendar P, Qu R, Kang W, He B, Yang G. Palladium-Catalyzed Cross-Coupling Reactions: A Powerful Tool for the Synthesis of Agrochemicals. J Agric Food Chem 2018;66:8914-34. [DOI: 10.1021/acs.jafc.8b03792] [Cited by in Crossref: 158] [Cited by in F6Publishing: 164] [Article Influence: 31.6] [Reference Citation Analysis]
Number Citing Articles
1 Baviskar BA, Ajmire PV, Chumbhale DS, Khan MS, Kuchake VG, Singupuram M, Laddha PR. Recent advances in nickel catalyzed Suzuki-Miyaura cross coupling reaction via C-O& C-N bond activation. Sustainable Chemistry and Pharmacy 2023;32:100953. [DOI: 10.1016/j.scp.2022.100953] [Reference Citation Analysis]
2 Martinek N, Morrison KM, Field JM, Fisher SA, Stradiotto M. Comparative Screening of DalPhos/Ni Catalysts in C-N Cross-couplings of (Hetero)aryl Chlorides Enables Development of Aminopyrazole Cross-couplings with Amine Base. Chemistry 2023;29:e202203394. [PMID: 36331074 DOI: 10.1002/chem.202203394] [Reference Citation Analysis]
3 Lokolkar MS, Kolekar YA, Jagtap PA, Bhanage BM. Cu-Catalyzed C-C Coupling Reactions. Topics in Organometallic Chemistry 2023. [DOI: 10.1007/3418_2022_81] [Reference Citation Analysis]
4 Sil S, Santha Bhaskaran A, Chakraborty S, Singh B, Kuniyil R, Mandal SK. Reduced-Phenalenyl-Based Molecule as a Super Electron Donor for Radical-Mediated C-N Coupling Catalysis at Room Temperature. J Am Chem Soc 2022. [PMID: 36450182 DOI: 10.1021/jacs.2c09225] [Reference Citation Analysis]
5 Lu D, Zou X, Li C. Advances in the application of named reactions in polymer synthesis. High Performance Polymers 2022. [DOI: 10.1177/09540083221143691] [Reference Citation Analysis]
6 Song G, Nong D, Li Q, Yan Y, Li G, Fan J, Zhang W, Cao R, Wang C, Xiao J, Xue D. Photochemical Synthesis of Anilines via Ni-Catalyzed Coupling of Aryl Halides with Ammonium Salts. ACS Catal 2022. [DOI: 10.1021/acscatal.2c04959] [Reference Citation Analysis]
7 Yu J, Jiang X. Synthesis and perspective of organosulfur chemicals in agrochemicals. Advanced Agrochem 2022. [DOI: 10.1016/j.aac.2022.12.003] [Reference Citation Analysis]
8 Tezcan B, Kemal Yılmaz M, Yakalı G, Aygün M, Güzel B. Palladium complexes of PNNP type diiminodiphosphine ligands for the Suzuki C C coupling reactions. Inorganica Chimica Acta 2022;543:121155. [DOI: 10.1016/j.ica.2022.121155] [Reference Citation Analysis]
9 Struwe J, Ackermann L, Gallou F. Recent progress in copper-free Sonogashira-Hagihara cross-couplings in water. Chem Catalysis 2022. [DOI: 10.1016/j.checat.2022.12.002] [Reference Citation Analysis]
10 Rodstein I, Kelling L, Löffler J, Scherpf T, Sarbajna A, Andrada DM, Gessner VH. Formation of exceptional monomeric YPhos-PdCl(2) complexes with high activities in coupling reactions. Chem Sci 2022;13:13552-62. [PMID: 36507159 DOI: 10.1039/d2sc04523k] [Reference Citation Analysis]
11 Rajasekaran H, Retnakaran A, Priyanka Dorairaj D, Karvembu R. Palladium(II) O^S thioamide complexes catalyzed Guerbet type reaction: β-alkylation of cyclohexanol with primary alcohols. Tetrahedron Letters 2022. [DOI: 10.1016/j.tetlet.2022.154248] [Reference Citation Analysis]
12 Nhari LM, Bifari EN, Al-marhabi AR, Al-ghamdi HA, Al-ghamdi SN, Al-zahrani FAM, Al-footy KO, El-shishtawy RM. Synthesis of Novel Key Chromophoric Intermediates via C-C Coupling Reactions. Catalysts 2022;12:1292. [DOI: 10.3390/catal12101292] [Reference Citation Analysis]
13 Ruffell K, Argent SP, Ling KB, Ball LT. Bismuth-Mediated α-Arylation of Acidic Diketones with ortho-Substituted Boronic Acids. Angew Chem Int Ed Engl 2022;61:e202210840. [PMID: 35950691 DOI: 10.1002/anie.202210840] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 3.0] [Reference Citation Analysis]
14 Mandal P, Pratihar JL. Chemistry of azo-imine based palladium complexes: a brief review. Reviews in Inorganic Chemistry 2022;0. [DOI: 10.1515/revic-2022-0017] [Reference Citation Analysis]
15 Mondal R, Guin AK, Paul ND. Heterocycles Synthesis by (Cross)‐Dehydrogenative Coupling. Handbook of CH‐Functionalization 2022. [DOI: 10.1002/9783527834242.chf0167] [Reference Citation Analysis]
16 Chen Y, Yang S, Zhang T, Xu M, Zhao J, Zeng M, Sun K, Feng R, Yang Z, Zhang P, Wang B, Cao X. Positron annihilation study of chitosan and its derived carbon/pillared montmorillonite clay stabilized Pd species nanocomposites. Polymer Testing 2022;114:107689. [DOI: 10.1016/j.polymertesting.2022.107689] [Reference Citation Analysis]
17 Vafaeezadeh M, Thiel WR. Task-Specific Janus Materials in Heterogeneous Catalysis. Angew Chem Int Ed Engl 2022;61:e202206403. [PMID: 35670287 DOI: 10.1002/anie.202206403] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
18 Forero Garzón AF, Joya Rodríguez S, Cachón Osorio KNS, Bernal Escobar AF, Gómez B, Sánchez-velandia JE, Mejía Chica SM. Estudio teórico de la oxidación de CO con O2 usando catalizadores de Au-Pd y Au-Pt. Rev Colomb Quim 2022;51. [DOI: 10.15446/rev.colomb.quim.v51n1.101015] [Reference Citation Analysis]
19 Gruselle M, Tõnsuaadu K, Gredin P, Len C. Hydroxyapatite‐Based Catalysts in Organic Synthesis. Design and Applications of Hydroxyapatite‐Based Catalysts 2022. [DOI: 10.1002/9783527830190.ch10] [Reference Citation Analysis]
20 Maru K, Kalla S, Jangir R. MOF/POM hybrids as catalysts for organic transformations. Dalton Trans 2022;51:11952-86. [PMID: 35916617 DOI: 10.1039/d2dt01895k] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
21 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]
22 Song G, Nong DZ, Li JS, Li G, Zhang W, Cao R, Wang C, Xiao J, Xue D. General Method for the Amination of Aryl Halides with Primary and Secondary Alkyl Amines via Nickel Photocatalysis. J Org Chem 2022. [PMID: 35877165 DOI: 10.1021/acs.joc.2c01284] [Reference Citation Analysis]
23 Belli RG, Tafuri VC, Roberts CC. Improving Alkyl–Alkyl Cross-Coupling Catalysis with Early Transition Metals through Mechanistic Understanding and Metal Tuning. ACS Catal . [DOI: 10.1021/acscatal.2c02785] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
24 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]
25 Setati B, Moshapo PT, Holzapfel CW, Maumela MC. Palladium-catalyzed Heck reactions promoted by limonene-derived bicyclic phosphines. Synthetic Communications. [DOI: 10.1080/00397911.2022.2093646] [Reference Citation Analysis]
26 Arora A, Oswal P, Rao GK, Kumar S, Singh AK, Kumar A. Tellurium-Ligated Pd(II) Complex of Bulky Organotellurium Ligand as a Catalyst of Suzuki coupling: First Report on In Situ Generation of Bimetallic Alloy ‘Telluropalladinite’ (Pd9Te4) Nanoparticles and Role in Highly Efficient Catalysis. Catal Lett 2022;152:1999-2011. [DOI: 10.1007/s10562-021-03769-4] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
27 Sadykova YM, Sennikova VV, Zalaltdinova AV, Burilov АR, Pudovik МА. New Bromine-Containing Symmetrical and Unsymmetrical Cage Phosphonates. Russ J Gen Chem 2022;92:1246-9. [DOI: 10.1134/s1070363222070118] [Reference Citation Analysis]
28 Toupalas G, Thomann G, Schlemper L, Rivero-crespo MA, Schmitt HL, Morandi B. Pd-Catalyzed Direct Deoxygenative Arylation of Non-π-Extended Benzyl Alcohols with Boronic Acids via Transient Formation of Non-Innocent Isoureas. ACS Catal . [DOI: 10.1021/acscatal.2c01858] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
29 Yang JF, Chen WJ, Zhou LM, Hewage KAH, Fu YX, Chen MX, He B, Pei RJ, Song K, Zhang JH, Yin J, Hao GF, Yang GF. Real-Time Fluorescence Imaging of the Abscisic Acid Receptor Allows Nondestructive Visualization of Plant Stress. ACS Appl Mater Interfaces 2022. [PMID: 35642545 DOI: 10.1021/acsami.2c02156] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
30 Sharma D, Arora A, Oswal P, Bahuguna A, Datta A, Kumar A. Organosulphur and organoselenium compounds as emerging building blocks for catalytic systems for O-arylation of phenols, a C-O coupling reaction. Dalton Trans 2022;51:8103-32. [PMID: 35535745 DOI: 10.1039/d1dt04371d] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
31 Yang X, Lu D, Guan W, Yin SF, Kambe N, Qiu R. Synthesis of (Deoxy)difluoromethylated Phosphines by Reaction of R2P(O)H with TMSCF3 and Their Application in Cu(I) Clusters in Sonogashira Coupling. J Org Chem 2022. [PMID: 35620903 DOI: 10.1021/acs.joc.2c00308] [Reference Citation Analysis]
32 Zhang X, Fang WY, Qin HL. Regio- and Stereoselective Installation of Bromide onto Vinyl Sulfonyl Fluorides: Construction of a Class of Versatile Sulfur Fluoride Exchange Hubs. Org Lett 2022. [PMID: 35622119 DOI: 10.1021/acs.orglett.2c01509] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
33 Engbers S, Hage R, Klein JEMN. Toward Environmentally Benign Electrophilic Chlorinations: From Chloroperoxidase to Bioinspired Isoporphyrins. Inorg Chem . [DOI: 10.1021/acs.inorgchem.2c00602] [Reference Citation Analysis]
34 Arora A, Oswal P, Datta A, Kumar A. Complexes of metals with organotellurium compounds and nanosized metal tellurides for catalysis, electrocatalysis and photocatalysis. Coordination Chemistry Reviews 2022;459:214406. [DOI: 10.1016/j.ccr.2022.214406] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 4.0] [Reference Citation Analysis]
35 Shalini C, Dharmaraj N, Bhuvanesh NS, Kaveri M. Suzuki Miyaura cross-coupling of 2-chloropyrazine with arylboronic acids catalyzed by novel palladium(II) ONO pincer complexes. Inorganica Chimica Acta 2022. [DOI: 10.1016/j.ica.2022.121028] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
36 Zhu JX, Chen ZC, Du W, Chen YC. Asymmetric Auto-Tandem Palladium Catalysis for 2,4-Dienyl Carbonates: Ligand-Controlled Divergent Synthesis. Angew Chem Int Ed Engl 2022;61:e202200880. [PMID: 35156289 DOI: 10.1002/anie.202200880] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
37 Uludağ N. A Simple and Efficient Acylation Reaction Over Zinc Triflate as a New Catalyst. European Journal of Science and Technology 2022. [DOI: 10.31590/ejosat.1083108] [Reference Citation Analysis]
38 Karna P, Okeke M, Meira DM, Finfrock Z, Yang D. Water-Soluble Palladium Nanoclusters as Catalysts in Ligand-Free Suzuki–Miyaura Cross-Coupling Reactions. ACS Appl Nano Mater 2022;5:3188-93. [DOI: 10.1021/acsanm.2c00389] [Reference Citation Analysis]
39 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]
40 Jayaraman S, Uthayanila S, Vanmathi C, Karthikeyan P. Metal-free convenient homogeneous bifunctional ionic liquid catalysed selective cross-hydrogenation ketone to alcohol. Materials Today Sustainability 2022;17:100102. [DOI: 10.1016/j.mtsust.2021.100102] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
41 Zhu J, Chen Z, Du W, Chen Y. Asymmetric Auto‐Tandem Palladium Catalysis for 2,4‐Dienyl Carbonates: Ligand‐Controlled Divergent Synthesis. Angewandte Chemie 2022;134. [DOI: 10.1002/ange.202200880] [Reference Citation Analysis]
42 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]
43 Hosseinzadeh R, Aghili N, Mavvaji M. Synthesis and characterization of nano-cellulose immobilized phenanthroline-copper (I) complex as a recyclable and efficient catalyst for preparation of diaryl ethers, N-aryl amides and N-aryl heterocycles. Polyhedron 2022;213:115631. [DOI: 10.1016/j.poly.2021.115631] [Reference Citation Analysis]
44 Rizzo G, Albano G, Sibillano T, Giannini C, Musio R, Omenetto FG, Farinola GM. Silk−Fibroin‐Supported Palladium Catalyst for Suzuki‐Miyaura and Ullmann Coupling Reactions of Aryl Chlorides. European J Organic Chem. [DOI: 10.1002/ejoc.202101567] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
45 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]
46 Walkowiak J, Szyling J, Franczyk A, Melen RL. Hydroelementation of diynes. Chem Soc Rev 2022. [PMID: 35005762 DOI: 10.1039/d1cs00485a] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 9.0] [Reference Citation Analysis]
47 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]
48 Attar SR, Kamble SB. Recent advances in nanoparticles towards sustainability and their application in organic transformations in aqueous media. Nanoscale 2022. [DOI: 10.1039/d2nr04148k] [Reference Citation Analysis]
49 Shi S, Wei J, Liang C, Bai H, Zhu H, Zhang Y, Fu F. Electro-oxidation induced O–S cross-coupling of quinoxalinones with sodium sulfinates for synthesizing 2-sulfonyloxylated quinoxalines. Chem Commun 2022. [DOI: 10.1039/d2cc04524a] [Reference Citation Analysis]
50 Díaz-sánchez M, Delgado-álvarez PN, Gómez IJ, Díaz-garcía D, Prashar S, Gómez-ruiz S. Modulation of the photocatalytic activity and crystallinity of F-TiO 2 nanoparticles by using green natural carboxylic acids. CrystEngComm. [DOI: 10.1039/d2ce00699e] [Reference Citation Analysis]
51 Chowdhury PR, Singha D, Sawoo S, Ghosh M, Pal N. Sonogashira Coupling Reaction and its Application in Dendrimer Synthesis. Asian J Chem 2022;34:1939-1957. [DOI: 10.14233/ajchem.2022.23748] [Reference Citation Analysis]
52 Van Emelen L, Henrion M, Lemmens R, De Vos D. C–N coupling reactions with arenes through C–H activation: the state-of-the-art versus the principles of green chemistry. Catal Sci Technol 2022;12:360-89. [DOI: 10.1039/d1cy01827b] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
53 Mirza-aghayan M, Mohammadi M, Boukherroub R. Synthesis and characterization of palladium nanoparticles immobilized on graphene oxide functionalized with triethylenetetramine or 2,6-diaminopyridine and application for the Suzuki cross-coupling reaction. Journal of Organometallic Chemistry 2022;957:122160. [DOI: 10.1016/j.jorganchem.2021.122160] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 5.0] [Reference Citation Analysis]
54 Marciniec B, Pietraszuk C, Pawluć P, Maciejewski H. Inorganometallics (Transition Metal-Metalloid Complexes) and Catalysis. Chem Rev 2021. [PMID: 34967210 DOI: 10.1021/acs.chemrev.1c00417] [Cited by in Crossref: 5] [Cited by in F6Publishing: 8] [Article Influence: 2.5] [Reference Citation Analysis]
55 Mohan M, Essalhi M, Zaye S, Rana LK, Maris T, Duong A. Hydrogen Bond Patterns of Dipyridone and Bis(Hydroxypyridinium) Cations. ACS Omega 2021;6:35649-56. [PMID: 34984296 DOI: 10.1021/acsomega.1c05561] [Reference Citation Analysis]
56 Kommuri VC, Tadiparthi K, Pawar L, Arunachalampillai A. A Simple and Efficient Ligand-Free Copper-Catalyzed C-N Bond Formation of Aryl (Hetero) Halides and N -Heteroaryl Amines. Polycyclic Aromatic Compounds. [DOI: 10.1080/10406638.2021.2019802] [Reference Citation Analysis]
57 Trowse BR, Byrne FP, Sherwood J, O’brien P, Murray J, Farmer TJ. 2,2,5,5-Tetramethyloxolane (TMO) as a Solvent for Buchwald–Hartwig Aminations. ACS Sustainable Chem Eng 2021;9:17330-7. [DOI: 10.1021/acssuschemeng.1c06292] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
58 Tsai JJ, Huang YH, Chou CM. Carboxylate-Assisted Palladium-Catalyzed Regio- and Stereoselective Mizoroki-Heck Arylation of β-Cyclohexadienyl Acrylates and Styrenes. Org Lett 2021;23:9468-73. [PMID: 34881572 DOI: 10.1021/acs.orglett.1c03650] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
59 Khan D, Parveen I, Shaily, Sharma S. Design, Synthesis and Characterization of Aurone Based α,β‐unsaturated Carbonyl‐Amino Ligands and their Application in Microwave Assisted Suzuki, Heck and Buchwald Reactions. Asian J Org Chem . [DOI: 10.1002/ajoc.202100638] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
60 Fan GG, Jiang BW, Sang W, Cheng H, Zhang R, Yu BY, Yuan Y, Chen C, Verpoort F. Metal-Free Synthesis of Heteroaryl Amines or Their Hydrochlorides via an External-Base-Free and Solvent-Free C-N Coupling Protocol. J Org Chem 2021;86:14627-39. [PMID: 34658240 DOI: 10.1021/acs.joc.1c01467] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
61 Payamifar S, Kazemi F, Kaboudin B. Nickel/β‐CD‐catalyzed Suzuki–Miyaura cross‐coupling of aryl boronic acids with aryl halides in water. Applied Organom Chemis 2021;35. [DOI: 10.1002/aoc.6378] [Reference Citation Analysis]
62 Okumura K, Morita S, Ohtsuki A, Takaba H. Inclusion of bidentate phosphine molecules in the supercage of FAU zeolite. Microporous and Mesoporous Materials 2021;327:111387. [DOI: 10.1016/j.micromeso.2021.111387] [Reference Citation Analysis]
63 Appleby KM, Dzotsi E, Scott NWJ, Dexin G, Jeddi N, Whitwood AC, Pridmore NE, Hart S, Duckett SB, Fairlamb IJS. Bridging the Gap from Mononuclear Pd II Precatalysts to Pd Nanoparticles: Identification of Intermediate Linear [Pd 3 (XPh 3 ) 4 ] 2+ Clusters as Catalytic Species for Suzuki–Miyaura Couplings (X = P, As). Organometallics 2021;40:3560-70. [DOI: 10.1021/acs.organomet.1c00452] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 3.0] [Reference Citation Analysis]
64 Ramos ITL, Silva RJM, Silva TMS, Camara CA. Palladium-catalyzed coupling reactions in flavonoids: A retrospective of recent synthetic approaches. Synthetic Communications 2021;51:3520-45. [DOI: 10.1080/00397911.2021.1988643] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
65 Sudharsan M, Nethaji M, Bhuvanesh NS, Suresh D. Heteroleptic Palladium(II) Complexes of Thiazolinyl‐picolinamide Derived N N N Pincer Ligand: An Efficient Catalyst for Acylative Suzuki Coupling Reactions. Asian J of Organic Chemis 2021;10:2982-92. [DOI: 10.1002/ajoc.202100490] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
66 Kohzadi H, Soleiman-Beigi M. Progress on the natural asphalt applications as a new class of carbonious heterogeneous support; synthesis of Na[Pd-NAS] and study of its catalytic activity in the formation of carbon-carbon bonds. Mol Divers 2021. [PMID: 34505952 DOI: 10.1007/s11030-021-10306-3] [Reference Citation Analysis]
67 Scalambra F, Lorenzo-luis P, de los Rios I, Romerosa A. New achievements on C-C bond formation in water catalyzed by metal complexes. Coordination Chemistry Reviews 2021;443:213997. [DOI: 10.1016/j.ccr.2021.213997] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]
68 Mccarthy S, Braddock DC, Wilton-ely JD. Strategies for sustainable palladium catalysis. Coordination Chemistry Reviews 2021;442:213925. [DOI: 10.1016/j.ccr.2021.213925] [Cited by in Crossref: 11] [Cited by in F6Publishing: 6] [Article Influence: 5.5] [Reference Citation Analysis]
69 Ferlin F, Valentini F, Sciosci D, Calamante M, Petricci E, Vaccaro L. Biomass Waste-Derived Pd–PiNe Catalyst for the Continuous-Flow Copper-Free Sonogashira Reaction in a CPME–Water Azeotropic Mixture. ACS Sustainable Chem Eng 2021;9:12196-204. [DOI: 10.1021/acssuschemeng.1c03634] [Cited by in Crossref: 5] [Cited by in F6Publishing: 7] [Article Influence: 2.5] [Reference Citation Analysis]
70 McCarthy S, Lee Wei Jie A, Braddock DC, Serpe A, Wilton-Ely JDET. From Waste to Green Applications: The Use of Recovered Gold and Palladium in Catalysis. Molecules 2021;26:5217. [PMID: 34500651 DOI: 10.3390/molecules26175217] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
71 Wong SM, Choy PY, Zhao Q, Yuen OY, Yeung CC, So CM, Kwong FY. Design of Benzimidazolyl Phosphines Bearing Alterable P , O or P , N -Coordination: Synthesis, Characterization, and Insights into Their Reactivity. Organometallics 2021;40:2265-71. [DOI: 10.1021/acs.organomet.0c00816] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
72 Li Y, Wang C, Chen Q, Li H, Su Y, Cheng T, Liu G, Tan C. Integrated Suzuki Cross-Coupling/Reduction Cascade Reaction of meta-/para-Chloroacetophenones and Arylboronic Acids under Batch and Continuous Flow Conditions. Chem Asian J 2021;16:2338-45. [PMID: 34190417 DOI: 10.1002/asia.202100479] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
73 Arora A, Singh S, Oswal P, Nautiyal D, Rao GK, Kumar S, Kumar A. Preformed molecular complexes of metals with organoselenium ligands: Syntheses and applications in catalysis. Coordination Chemistry Reviews 2021;438:213885. [DOI: 10.1016/j.ccr.2021.213885] [Cited by in Crossref: 22] [Cited by in F6Publishing: 24] [Article Influence: 11.0] [Reference Citation Analysis]
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