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For: Sutar RL, Huber SM. Catalysis of Organic Reactions through Halogen Bonding. ACS Catal 2019;9:9622-39. [DOI: 10.1021/acscatal.9b02894] [Cited by in Crossref: 146] [Cited by in F6Publishing: 86] [Article Influence: 48.7] [Reference Citation Analysis]
Number Citing Articles
1 Chernysheva MV, Rautiainen JM, Ding X, Haukka M. The Se … Hal halogen bonding: Co-crystals of selenoureas with fluorinated organohalides. Journal of Solid State Chemistry 2021;295:121930. [DOI: 10.1016/j.jssc.2020.121930] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
2 Tong Q, Zhao Z, Wang Y. A Se···O bonding catalysis approach to the synthesis of calix[4]pyrroles. Beilstein J Org Chem 2022;18:325-30. [DOI: 10.3762/bjoc.18.36] [Reference Citation Analysis]
3 Sutar RL, Engelage E, Stoll R, Huber SM. Zweizähnige chirale Bis(imidazolium)‐basierte Halogenbrückendonoren: Synthese und Anwendungen in enantioselektiver Erkennung und Katalyse. Angew Chem 2020;132:6872-7. [DOI: 10.1002/ange.201915931] [Cited by in Crossref: 11] [Cited by in F6Publishing: 4] [Article Influence: 5.5] [Reference Citation Analysis]
4 Portela S, Fernández I. Nature of C−I⋅⋅⋅π Halogen Bonding and its Role in Organocatalysis. Eur J Org Chem 2021;2021:6102-10. [DOI: 10.1002/ejoc.202101244] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
5 Dumitrescu D, Shova S, Man IC, Caira MR, Popa MM, Dumitrascu F. 5-Iodo-1-Arylpyrazoles as Potential Benchmarks for Investigating the Tuning of the Halogen Bonding. Crystals 2020;10:1149. [DOI: 10.3390/cryst10121149] [Cited by in Crossref: 8] [Cited by in F6Publishing: 5] [Article Influence: 4.0] [Reference Citation Analysis]
6 Gurbanov AV, Kuznetsov ML, Karmakar A, Aliyeva VA, Mahmudov KT, Pombeiro AJL. Halogen bonding in cadmium(II) MOFs: its influence on the structure and on the nitroaldol reaction in aqueous medium. Dalton Trans 2021. [PMID: 34935834 DOI: 10.1039/d1dt03755b] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
7 Abe T, Hirao S. Rapid access to indole-fused bicyclo[2.2.2]octanones by merging the umpolung strategy and molecular iodine as a green catalyst. Org Biomol Chem 2020;18:4193-7. [PMID: 32458925 DOI: 10.1039/d0ob01038c] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
8 Momiyama N, Izumiseki A, Ohtsuka N, Suzuki T. Correlations between Substituent Effects and Catalytic Activities: A Quantitative Approach for the Development of Halogen-Bonding-Driven Anion-Binding Catalysts. Chempluschem 2021;86:913-9. [PMID: 34145787 DOI: 10.1002/cplu.202100147] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
9 Aliyarova IS, Ivanov DM, Soldatova NS, Novikov AS, Postnikov PS, Yusubov MS, Kukushkin VY. Bifurcated Halogen Bonding Involving Diaryliodonium Cations as Iodine(III)-Based Double-σ-Hole Donors. Crystal Growth & Design 2021;21:1136-47. [DOI: 10.1021/acs.cgd.0c01463] [Cited by in Crossref: 8] [Cited by in F6Publishing: 6] [Article Influence: 8.0] [Reference Citation Analysis]
10 Zhu Y, Shi J, Yu W. Photoinduced Site-Selective C(sp 3 )–H Chlorination of Aliphatic Amides. Org Lett 2020;22:8899-903. [DOI: 10.1021/acs.orglett.0c03297] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
11 Sawaguchi D, Hayakawa S, Sakuma M, Niitsuma K, Kase D, Michii S, Ozawa M, Sakai Y, Sakamaki K, Ueyama K, Haraguchi R. Improved Synthesis of 1,2,3‐Triazolium Salts via Oxidative [3+2] Cycloaddition of Triazenes with Alkynes and Their Deprotonative Functionalization. Asian J of Organic Chemis 2021;10:901-5. [DOI: 10.1002/ajoc.202100033] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
12 Sutar RL, Huber * SM. Catalysis by Halogen Bonding Based on Iodine. In: Ishihara K, Muñiz K, editors. Iodine Catalysis in Organic Synthesis. Wiley; 2022. pp. 27-67. [DOI: 10.1002/9783527829569.ch3] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
13 Liu X, Toy PH. Halogen Bond‐Catalyzed Povarov Reactions. Adv Synth Catal 2020;362:3437-41. [DOI: 10.1002/adsc.202000665] [Cited by in Crossref: 9] [Cited by in F6Publishing: 2] [Article Influence: 4.5] [Reference Citation Analysis]
14 Sarkar S, Sarkar P, Munshi S, Ghosh P. One-Pot Dual C-C Coupling Reaction via Site Selective Cascade Formation by PdII -Cryptate of an Amino-Ether Heteroditopic Macrobicycle. Chemistry 2021;27:7307-14. [PMID: 33439499 DOI: 10.1002/chem.202005397] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
15 Berger G, Frangville P, Meyer F. Halogen bonding for molecular recognition: new developments in materials and biological sciences. Chem Commun 2020;56:4970-81. [DOI: 10.1039/d0cc00841a] [Cited by in Crossref: 41] [Cited by in F6Publishing: 3] [Article Influence: 20.5] [Reference Citation Analysis]
16 Yan W, Zheng M, Xu C, Chen F. Harnessing noncovalent interaction of chalcogen bond in organocatalysis: From the catalyst point of view. Green Synthesis and Catalysis 2021;2:329-36. [DOI: 10.1016/j.gresc.2021.08.002] [Cited by in Crossref: 2] [Article Influence: 2.0] [Reference Citation Analysis]
17 Yang Q, Yang F, Zhang Y, Hou J, Li J, Cheng J, Wu S, Zhan H, Zhang X, Shi H. Anchored PdCl2 on fish scale: an efficient and recyclable catalyst for Suzuki coupling reaction in aqueous media. Journal of Organometallic Chemistry 2021;933:121656. [DOI: 10.1016/j.jorganchem.2020.121656] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
18 von der Heiden D, Rissanen K, Erdélyi M. Asymmetric [N–I–N] + halonium complexes in solution? Chem Commun 2020;56:14431-4. [DOI: 10.1039/d0cc06706g] [Cited by in Crossref: 8] [Article Influence: 4.0] [Reference Citation Analysis]
19 Kuwano S, Nishida Y, Suzuki T, Arai T. Catalytic Asymmetric Mannich‐Type Reaction of Malononitrile with N‐Boc α‐Ketiminoesters Using Chiral Organic Base Catalyst with Halogen Bond Donor Functionality. Adv Synth Catal 2020;362:1674-8. [DOI: 10.1002/adsc.202000092] [Cited by in Crossref: 16] [Cited by in F6Publishing: 6] [Article Influence: 8.0] [Reference Citation Analysis]
20 Liu X, Ma S, Toy PH. Halogen Bond-Catalyzed Friedel–Crafts Reactions of Aldehydes and Ketones Using a Bidentate Halogen Bond Donor Catalyst: Synthesis of Symmetrical Bis(indolyl)methanes. Org Lett 2019;21:9212-6. [DOI: 10.1021/acs.orglett.9b03578] [Cited by in Crossref: 21] [Cited by in F6Publishing: 11] [Article Influence: 7.0] [Reference Citation Analysis]
21 Haraguchi R, Nishikawa T, Kanazawa A, Aoshima S. Metal-Free Living Cationic Polymerization Using Diaryliodonium Salts as Organic Lewis Acid Catalysts. Macromolecules 2020;53:4185-92. [DOI: 10.1021/acs.macromol.0c00823] [Cited by in Crossref: 16] [Cited by in F6Publishing: 7] [Article Influence: 8.0] [Reference Citation Analysis]
22 Panikkattu VV, Huber AS, Sinha AS, Averkiev BB, Aakeröy CB. “Triply Activated” Phenyl 3-Iodopropiolates: Halogen-Bond Donors with Remarkable σ-Hole Potentials. Crystal Growth & Design. [DOI: 10.1021/acs.cgd.1c01450] [Reference Citation Analysis]
23 Schumacher C, Fergen H, Puttreddy R, Truong K, Rinesch T, Rissanen K, Bolm C. N -(2,3,5,6-Tetrafluoropyridyl)sulfoximines: synthesis, X-ray crystallography, and halogen bonding. Org Chem Front 2020;7:3896-906. [DOI: 10.1039/d0qo01139h] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
24 Loh CCJ. Exploiting non-covalent interactions in selective carbohydrate synthesis. Nat Rev Chem 2021;5:792-815. [DOI: 10.1038/s41570-021-00324-y] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
25 Novikov AS, Gushchin AL. THEORETICAL INVESTIGATION OF SUPRAMOLECULAR Br···Br AND I···I CONTACTS IN TITANIUM, VANADIUM, AND TANTALUM CHALCOGENIDES. J Struct Chem 2021;62:1325-31. [DOI: 10.1134/s0022476621090018] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
26 Miller DK, Loy C, Rosokha SV. Examining a Transition from Supramolecular Halogen Bonding to Covalent Bonds: Topological Analysis of Electron Densities and Energies in the Complexes of Bromosubstituted Electrophiles. ACS Omega 2021;6:23588-97. [PMID: 34549156 DOI: 10.1021/acsomega.1c03779] [Cited by in Crossref: 3] [Article Influence: 3.0] [Reference Citation Analysis]
27 Gao X, Chang R, Rao J, Hao D, Zhang Z, Zhou CY, Guo Z. Halogen-Bonding-Promoted C-H Malonylation of Indoles under Visible-Light Irradiation. J Org Chem 2022. [PMID: 35612828 DOI: 10.1021/acs.joc.2c00413] [Reference Citation Analysis]
28 Nishida Y, Suzuki T, Takagi Y, Amma E, Tajima R, Kuwano S, Arai T. A Hypervalent Cyclic Dibenzoiodolium Salt as a Halogen-Bond-Donor Catalyst for the [4+2] Cycloaddition of 2-Alkenylindoles. Chempluschem 2021;86:741-4. [PMID: 33942571 DOI: 10.1002/cplu.202100089] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
29 Alvarez MS, Houzé C, Groni S, Schöllhorn B, Fave C. Halogen bonding effect on electrochemical anion oxidation in ionic liquids. Org Biomol Chem 2021;19:7587-93. [PMID: 34524327 DOI: 10.1039/d1ob01031j] [Reference Citation Analysis]
30 Torubaev YV, Skabitsky IV, Rozhkov AV, Galmés B, Frontera A, Kukushkin VY. Highly polar stacking interactions wrap inorganics in organics: lone-pair–π-hole interactions between the PdO 4 core and electron-deficient arenes. Inorg Chem Front 2021;8:4965-75. [DOI: 10.1039/d1qi01067k] [Cited by in Crossref: 7] [Cited by in F6Publishing: 4] [Article Influence: 7.0] [Reference Citation Analysis]
31 Muñoz-Castro A, Wang G, Ponduru TT, Dias HVR. Synthesis and characterization of N-heterocyclic carbene-MOEt2 complexes (M = Cu, Ag, Au). Analysis of solvated auxiliary-ligand free [(NHC)M]+ species. Phys Chem Chem Phys 2021;23:1577-83. [PMID: 33406199 DOI: 10.1039/d0cp05222a] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
32 Proctor RSJ, Colgan AC, Phipps RJ. Exploiting attractive non-covalent interactions for the enantioselective catalysis of reactions involving radical intermediates. Nat Chem 2020;12:990-1004. [DOI: 10.1038/s41557-020-00561-6] [Cited by in Crossref: 21] [Cited by in F6Publishing: 11] [Article Influence: 10.5] [Reference Citation Analysis]
33 Breugst M, Koenig JJ. σ‐Hole Interactions in Catalysis. Eur J Org Chem 2020;2020:5473-87. [DOI: 10.1002/ejoc.202000660] [Cited by in Crossref: 33] [Cited by in F6Publishing: 15] [Article Influence: 16.5] [Reference Citation Analysis]
34 Hosseinijei R, Zahedian Tejeneki H, Nikbakht A, Rominger F, Balalaie S. Synthesis of functionalized 1-aminoisoquinolines through cascade three-component reaction of ortho-alkynylbenzaldoximes, 2H-azirines, and electrophiles. Org Biomol Chem 2022;20:3076-80. [PMID: 35352735 DOI: 10.1039/d2ob00275b] [Reference Citation Analysis]
35 Jiang L, Yu L, Peng P, Li H, Jiang D, Wang Y, Yuan M, Yuan M. Stereoselective allylic 1,3-dienylation of Morita–Baylis–Hillman carbonates via an alkylation–denitration sequence. Synthetic Communications 2021;51:419-27. [DOI: 10.1080/00397911.2020.1832526] [Reference Citation Analysis]
36 Pace DP, Robidas R, Tran UPN, Legault CY, Nguyen TV. Iodine-Catalyzed Synthesis of Substituted Furans and Pyrans: Reaction Scope and Mechanistic Insights. J Org Chem 2021;86:8154-71. [PMID: 34048250 DOI: 10.1021/acs.joc.1c00608] [Reference Citation Analysis]
37 Docker A, Guthrie CH, Kuhn H, Beer PD. Modulating Chalcogen Bonding and Halogen Bonding Sigma‐Hole Donor Atom Potency and Selectivity for Halide Anion Recognition. Angewandte Chemie 2021;133:22144-9. [DOI: 10.1002/ange.202108591] [Cited by in Crossref: 2] [Article Influence: 2.0] [Reference Citation Analysis]
38 Peintner S, Erdélyi M. Pushing the Limits of Characterising a Weak Halogen Bond in Solution. Chemistry 2021. [PMID: 34807488 DOI: 10.1002/chem.202103559] [Reference Citation Analysis]
39 Arndt T, Wagner PK, Koenig JJ, Breugst M. Iodine‐Catalyzed Diels‐Alder Reactions. ChemCatChem 2021;13:2922-30. [DOI: 10.1002/cctc.202100342] [Cited by in Crossref: 3] [Article Influence: 3.0] [Reference Citation Analysis]
40 Yoshida Y, Mino T, Sakamoto M. Chiral Hypervalent Bromine(III) (Bromonium Salt): Hydrogen- and Halogen-Bonding Bifunctional Asymmetric Catalysis by Diaryl-λ 3 -bromanes. ACS Catal 2021;11:13028-33. [DOI: 10.1021/acscatal.1c04070] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 5.0] [Reference Citation Analysis]
41 Soldatova NS, Suslonov VV, Kissler TY, Ivanov DM, Novikov AS, Yusubov MS, Postnikov PS, Kukushkin VY. Halogen Bonding Provides Heterooctameric Supramolecular Aggregation of Diaryliodonium Thiocyanate. Crystals 2020;10:230. [DOI: 10.3390/cryst10030230] [Cited by in Crossref: 9] [Cited by in F6Publishing: 5] [Article Influence: 4.5] [Reference Citation Analysis]
42 Weiss R, Golisano T, Pale P, Mamane V. Insight into the Modes of Activation of Pyridinium and Bipyridinium Salts in Non‐Covalent Organocatalysis. Adv Synth Catal 2021;363:4779-88. [DOI: 10.1002/adsc.202100865] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
43 Reinhard DL, Heinen F, Stoesser J, Engelage E, Huber SM. Tuning the Halogen Bonding Strength of Cyclic Diaryliodonium Salts. Helv Chim Acta 2021;104. [DOI: 10.1002/hlca.202000221] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 4.0] [Reference Citation Analysis]
44 Jónsson HF, Sethio D, Wolf J, Huber SM, Fiksdahl A, Erdelyi M. Halogen Bond Activation in Gold Catalysis. ACS Catal . [DOI: 10.1021/acscatal.2c01864] [Reference Citation Analysis]
45 Tasnim T, Ryan C, Christensen ML, Fennell CJ, Pitre SP. Radical Perfluoroalkylation Enabled by a Catalytically Generated Halogen Bonding Complex and Visible Light Irradiation. Org Lett 2021. [PMID: 34914870 DOI: 10.1021/acs.orglett.1c04139] [Reference Citation Analysis]
46 Robidas R, Reinhard DL, Legault CY, Huber SM. Iodine(III)-Based Halogen Bond Donors: Properties and Applications. Chem Rec 2021;21:1912-27. [PMID: 34145711 DOI: 10.1002/tcr.202100119] [Cited by in Crossref: 2] [Article Influence: 2.0] [Reference Citation Analysis]
47 Kato N, Nanjo T, Takemoto Y. A Pyridine-Based Donor–Acceptor Molecule: A Highly Reactive Organophotocatalyst That Enables the Reductive Cleavage of C–Br Bonds through Halogen Bonding. ACS Catal . [DOI: 10.1021/acscatal.2c02067] [Reference Citation Analysis]
48 Bondarenko MA, Abramov PA, Novikov AS, Sokolov MN, Adonin SA. Cu(II) pentaiodobenzoate complexes: “super heavy carboxylates” featuring strong halogen bonding. Polyhedron 2022;214:115644. [DOI: 10.1016/j.poly.2021.115644] [Reference Citation Analysis]
49 Takagi K, Murakata H, Hasegawa T. Application of Thiourea/Halogen Bond Donor Cocatalysis in Metal-Free Cationic Polymerization of Isobutyl Vinyl Ether and Styrene Derivatives. Macromolecules. [DOI: 10.1021/acs.macromol.2c00281] [Reference Citation Analysis]
50 Southern SA, Nag T, Kumar V, Triglav M, Levin K, Bryce DL. NMR Response of the Tetrel Bond Donor. J Phys Chem C 2022;126:851-65. [DOI: 10.1021/acs.jpcc.1c10121] [Reference Citation Analysis]
51 Wang Y, Su P. Why Can Cationic Halogen Bond Donors Activate the Ritter-Type Solvolysis of Benzhydryl Bromide but Cationic Hydrogen Bond Donors Can Not? ACS Omega 2020;5:21862-72. [PMID: 32905280 DOI: 10.1021/acsomega.0c03000] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
52 Wang C, Chong AML, Pan HM, Sarkar J, Tay XT, Goto A. Recent development in halogen-bonding-catalyzed living radical polymerization. Polym Chem 2020;11:5559-71. [DOI: 10.1039/d0py00939c] [Cited by in Crossref: 19] [Article Influence: 9.5] [Reference Citation Analysis]
53 Mamane V, Peluso P, Aubert E, Weiss R, Wenger E, Cossu S, Pale P. Disubstituted Ferrocenyl Iodo- and Chalcogenoalkynes as Chiral Halogen and Chalcogen Bond Donors. Organometallics 2020;39:3936-50. [DOI: 10.1021/acs.organomet.0c00633] [Cited by in Crossref: 15] [Cited by in F6Publishing: 9] [Article Influence: 7.5] [Reference Citation Analysis]
54 Fanourakis A, Docherty PJ, Chuentragool P, Phipps RJ. Recent Developments in Enantioselective Transition Metal Catalysis Featuring Attractive Noncovalent Interactions between Ligand and Substrate. ACS Catal 2020;10:10672-714. [PMID: 32983588 DOI: 10.1021/acscatal.0c02957] [Cited by in Crossref: 49] [Cited by in F6Publishing: 34] [Article Influence: 24.5] [Reference Citation Analysis]
55 Li J, Kwon E, Lear MJ, Hayashi Y. Halogen Bonding of N ‐Halosuccinimides with Amines and Effects of Brønsted Acids in Quinuclidine‐Catalyzed Halocyclizations. Helv Chim Acta 2021;104. [DOI: 10.1002/hlca.202100080] [Reference Citation Analysis]
56 Fortuna A, Costa PJ. Optimized Halogen Atomic Radii for PBSA Calculations Using Off-Center Point Charges. J Chem Inf Model 2021;61:3361-75. [PMID: 34185532 DOI: 10.1021/acs.jcim.1c00177] [Reference Citation Analysis]
57 Ivanov DM, Bokach NA, Yu Kukushkin V, Frontera A. Metal Centers as Nucleophiles: Oxymoron of Halogen Bond-Involving Crystal Engineering. Chemistry 2021. [PMID: 34623005 DOI: 10.1002/chem.202103173] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
58 Kriis K, Martõnov H, Miller A, Erkman K, Järving I, Kaasik M, Kanger T. Multifunctional Catalysts in the Asymmetric Mannich Reaction of Malononitrile with N-Phosphinoylimines: Coactivation by Halogen Bonding versus Hydrogen Bonding. J Org Chem 2022;87:7422-35. [PMID: 35594434 DOI: 10.1021/acs.joc.2c00674] [Reference Citation Analysis]
59 Czarny RS, Ho AN, Shing Ho P. A Biological Take on Halogen Bonding and Other Non-Classical Non-Covalent Interactions. Chem Rec 2021;21:1240-51. [PMID: 33886153 DOI: 10.1002/tcr.202100076] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
60 Lee R, Eric Chao CB, Ban X, Tan SM, Yu H, Hyland CJT, Tan CH. Direct SN2 or SN2X Manifold─Mechanistic Study of Ion-Pair-Catalyzed Carbon(sp3)-Carbon(sp3) Bond Formation. J Org Chem 2022. [PMID: 35245425 DOI: 10.1021/acs.joc.1c02782] [Reference Citation Analysis]
61 Takagi K, Sakakibara N, Kikkawa S, Tsuzuki S. Dicationic oligotelluroxane or mononuclear telluronium cation? Elucidation of the true catalytic species and activation mechanism of the benzylic carbon-halogen bond. Chem Commun (Camb) 2021;57:13736-9. [PMID: 34843614 DOI: 10.1039/d1cc06311a] [Reference Citation Analysis]
62 Hein R, Docker A, Davis JJ, Beer PD. Redox-Switchable Chalcogen Bonding for Anion Recognition and Sensing. J Am Chem Soc 2022. [PMID: 35522996 DOI: 10.1021/jacs.2c02924] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
63 Soldatova NS, Postnikov PS, Suslonov VV, Kissler TY, Ivanov DM, Yusubov MS, Galmés B, Frontera A, Kukushkin VY. Diaryliodonium as a double σ-hole donor: the dichotomy of thiocyanate halogen bonding provides divergent solid state arylation by diaryliodonium cations. Org Chem Front 2020;7:2230-42. [DOI: 10.1039/d0qo00678e] [Cited by in Crossref: 16] [Cited by in F6Publishing: 4] [Article Influence: 8.0] [Reference Citation Analysis]
64 Weiss R, Aubert E, Pale P, Mamane V. Chalcogen-Bonding Catalysis with Telluronium Cations. Angew Chem Int Ed Engl 2021;60:19281-6. [PMID: 34166563 DOI: 10.1002/anie.202105482] [Cited by in Crossref: 4] [Cited by in F6Publishing: 1] [Article Influence: 4.0] [Reference Citation Analysis]
65 Sterling AJ, Zavitsanou S, Ford J, Duarte F. Selectivity in organocatalysis—From qualitative to quantitative predictive models. WIREs Comput Mol Sci 2021;11. [DOI: 10.1002/wcms.1518] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
66 Sysoeva AA, Novikov AS, Il'in MV, Suslonov VV, Bolotin DS. Predicting the catalytic activity of azolium-based halogen bond donors: an experimentally-verified theoretical study. Org Biomol Chem 2021;19:7611-20. [PMID: 34323914 DOI: 10.1039/d1ob01158h] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
67 Il'in MV, Sysoeva AA, Novikov AS, Bolotin DS. Diaryliodoniums as Hybrid Hydrogen- and Halogen-Bond-Donating Organocatalysts for the Groebke-Blackburn-Bienaymé Reaction. J Org Chem 2022. [PMID: 35176856 DOI: 10.1021/acs.joc.1c02885] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
68 Zhang X, Tan C. Stereospecific and stereoconvergent nucleophilic substitution reactions at tertiary carbon centers. Chem 2021;7:1451-86. [DOI: 10.1016/j.chempr.2020.11.022] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
69 Sutar RL, Erochok N, Huber SM. Mukaiyama aldol reaction catalyzed by (benz)imidazolium-based halogen bond donors. Org Biomol Chem 2021;19:770-4. [PMID: 33432958 DOI: 10.1039/d0ob02503h] [Cited by in Crossref: 3] [Article Influence: 3.0] [Reference Citation Analysis]
70 Lindblad S, Németh FB, Földes T, Vanderkooy A, Pápai I, Erdélyi M. O-I-O halogen bond of halonium ions. Chem Commun (Camb) 2020;56:9671-4. [PMID: 32696769 DOI: 10.1039/d0cc03513k] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
71 Bouayad‐gervais S, Scattolin T, Schoenebeck F. N ‐Trifluoromethyl Hydrazines, Indoles and Their Derivatives. Angew Chem 2020;132:12006-10. [DOI: 10.1002/ange.202004321] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
72 Portela S, Cabrera-trujillo JJ, Fernández I. Catalysis by Bidentate Iodine(III)-Based Halogen Donors: Surpassing the Activity of Strong Lewis Acids. J Org Chem 2021;86:5317-26. [DOI: 10.1021/acs.joc.1c00534] [Cited by in Crossref: 5] [Cited by in F6Publishing: 2] [Article Influence: 5.0] [Reference Citation Analysis]
73 Baykov SV, Semenov AV, Presnukhina SI, Novikov AS, Shetnev AA, Boyarskiy VP. Hydrogen vs. halogen bonding in crystals of 2,5-dibromothiophene-3-carboxylic acid derivatives. Journal of Molecular Structure 2022;1260:132785. [DOI: 10.1016/j.molstruc.2022.132785] [Reference Citation Analysis]
74 Riel AMS, Decato DA, Sun J, Berryman OB. Halogen bonding organocatalysis enhanced through intramolecular hydrogen bonds. Chem Commun (Camb) 2022;58:1378-81. [PMID: 34989732 DOI: 10.1039/d1cc05475a] [Reference Citation Analysis]
75 Jalilov A, Deats S, Albukhari M, Zeller M, Rosokha SV. Intermolecular Interactions between Halogen‐Substituted p ‐Benzoquinones and Halide Anions: Anion‐π Complexes versus Halogen Bonding. ChemPlusChem 2020;85:441-9. [DOI: 10.1002/cplu.202000012] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
76 Korobeynikov NA, Usoltsev AN, Abramov PA, Novikov AS, Sokolov MN, Adonin SA. Bromine-rich tin(IV) halide complexes: Experimental and theoretical examination of Br···Br noncovalent interactions in crystalline state. Polyhedron 2022;222:115912. [DOI: 10.1016/j.poly.2022.115912] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
77 Kobayashi Y, Masakado S, Murai T, Hamada S, Furuta T, Takemoto Y. A bench-stable N-trifluoroacetyl nitrene equivalent for a simple synthesis of 2-trifluoromethyl oxazoles. Org Biomol Chem 2021;19:6628-32. [PMID: 34282812 DOI: 10.1039/d1ob00947h] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
78 Yunusova SN, Novikov AS, Soldatova NS, Vovk MA, Bolotin DS. Iodonium salts as efficient iodine( iii )-based noncovalent organocatalysts for Knorr-type reactions. RSC Adv 2021;11:4574-83. [DOI: 10.1039/d0ra09640g] [Cited by in Crossref: 5] [Article Influence: 5.0] [Reference Citation Analysis]
79 Mahmudov KT, Aliyeva VA, Guedes da Silva MFC, Pombeiro AJL. The Chalcogen Bond in Solution: Synthesis, Catalysis and Molecular Recognition. In: Huber S, editor. Halogen Bonding in Solution. Wiley; 2021. pp. 363-82. [DOI: 10.1002/9783527825738.ch11] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
80 Chang YP, Tang T, Jagannathan JR, Hirbawi N, Sun S, Brown J, Franz AK. NMR Quantification of Halogen-Bonding Ability To Evaluate Catalyst Activity. Org Lett 2020;22:6647-52. [PMID: 32806211 DOI: 10.1021/acs.orglett.0c02427] [Cited by in Crossref: 7] [Cited by in F6Publishing: 1] [Article Influence: 3.5] [Reference Citation Analysis]
81 Zhu L, Yang H, Wong MW. Asymmetric Nucleophilic Allylation of α-Chloro Glycinate via Squaramide Anion-Abstraction Catalysis: S N 1 or S N 2 Mechanism, or Both? J Org Chem 2021;86:8414-24. [DOI: 10.1021/acs.joc.1c00839] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
82 Tarannam N, Shukla R, Kozuch S. Yet another perspective on hole interactions. Phys Chem Chem Phys 2021;23:19948-63. [PMID: 34514473 DOI: 10.1039/d1cp03533a] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
83 Kimura T, Hamada S, Furuta T, Takemoto Y, Kobayashi Y. N-Acylimino-λ3-iodanes from the Metathesis of Iodosoarenes and Nitriles for the Photoinduced C-H Perfluoroacylamination of (Hetero)Arenes. Org Lett 2022. [PMID: 35758853 DOI: 10.1021/acs.orglett.2c02054] [Reference Citation Analysis]
84 Trouvé J, Gramage-doria R. Beyond hydrogen bonding: recent trends of outer sphere interactions in transition metal catalysis. Chem Soc Rev 2021;50:3565-84. [DOI: 10.1039/d0cs01339k] [Cited by in Crossref: 10] [Article Influence: 10.0] [Reference Citation Analysis]
85 Chernysheva MV, Bulatova M, Ding X, Haukka M. Influence of Substituents in the Aromatic Ring on the Strength of Halogen Bonding in Iodobenzene Derivatives. Crystal Growth & Design 2020;20:7197-210. [DOI: 10.1021/acs.cgd.0c00866] [Cited by in Crossref: 8] [Cited by in F6Publishing: 2] [Article Influence: 4.0] [Reference Citation Analysis]
86 Suzuki T, Kuwano S, Arai T. Non‐Bonding Electron Pair versus π‐Electrons in Solution Phase Halogen Bond Catalysis: Povarov Reaction of 2‐Vinylindoles and Imines. Adv Synth Catal 2020;362:3208-12. [DOI: 10.1002/adsc.202000494] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 2.5] [Reference Citation Analysis]
87 Matern J, Bäumer N, Fernández G. Unraveling Halogen Effects in Supramolecular Polymerization. J Am Chem Soc 2021;143:7164-75. [PMID: 33913728 DOI: 10.1021/jacs.1c02384] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
88 Torita K, Haraguchi R, Morita Y, Kemmochi S, Komatsu T, Fukuzawa S. Lewis acid–base synergistic catalysis of cationic halogen-bonding-donors with nucleophilic counter anions. Chem Commun 2020;56:9715-8. [DOI: 10.1039/d0cc04013d] [Cited by in Crossref: 9] [Article Influence: 4.5] [Reference Citation Analysis]
89 Nemec V, Lisac K, Bedeković N, Fotović L, Stilinović V, Cinčić D. Crystal engineering strategies towards halogen-bonded metal–organic multi-component solids: salts, cocrystals and salt cocrystals. CrystEngComm 2021;23:3063-83. [DOI: 10.1039/d1ce00158b] [Cited by in Crossref: 26] [Cited by in F6Publishing: 7] [Article Influence: 26.0] [Reference Citation Analysis]
90 Lim B, Cheng Y, Kato T, Pham A, Le Du E, Mishra AK, Grinhagena E, Moreau D, Sakai N, Waser J, Matile S. Inhibition of Thiol‐Mediated Uptake with Irreversible Covalent Inhibitors. Helv Chim Acta 2021;104. [DOI: 10.1002/hlca.202100085] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
91 Paraja M, Gini A, Sakai N, Matile S. Pnictogen‐Bonding Catalysis: An Interactive Tool to Uncover Unorthodox Mechanisms in Polyether Cascade Cyclizations. Chem Eur J 2020;26:15471-6. [DOI: 10.1002/chem.202003426] [Cited by in Crossref: 10] [Cited by in F6Publishing: 7] [Article Influence: 5.0] [Reference Citation Analysis]
92 Sharutin VV, Sharutina OK, Novikov AS, Adonin SA. Substituent-dependent reactivity of triarylantimony( iii ) toward I 2 : isolation of [Ar 3 SbI] + salt. New J Chem 2020;44:14339-42. [DOI: 10.1039/d0nj02774j] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
93 Kuwano S, Ogino E, Arai T. Enantio- and diastereoselective double Mannich reaction of malononitrile with N-Boc imines using quinine-derived bifunctional organoiodine catalyst. Org Biomol Chem 2021;19:6969-73. [PMID: 34337640 DOI: 10.1039/d1ob00796c] [Reference Citation Analysis]
94 Heinen F, Reinhard DL, Engelage E, Huber SM. Ein zweizähniger Iod(III)‐basierter Halogenbrückendonor als leistungsfähiger Organokatalysator**. Angew Chem 2021;133:5127-32. [DOI: 10.1002/ange.202013172] [Cited by in Crossref: 5] [Cited by in F6Publishing: 1] [Article Influence: 5.0] [Reference Citation Analysis]
95 Bunchuay T, Boonpalit K, Docker A, Ruengsuk A, Tantirungrotechai J, Sukwattanasinitt M, Surawatanawong P, Beer PD. Charge neutral halogen bonding tetradentate-iodotriazole macrocycles capable of anion recognition and sensing in highly competitive aqueous media. Chem Commun (Camb) 2021;57:11976-9. [PMID: 34708850 DOI: 10.1039/d1cc05037k] [Reference Citation Analysis]