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12 Veliks J, Videja M, Kinens A, Bobrovs R, Priede M, Kuka J. trans-Fluorine Effect in Cyclopropane: Diastereoselective Synthesis of Fluorocyclopropyl Cabozantinib Analogs. ACS Med Chem Lett 2020;11:2146-50. [PMID: 33214822 DOI: 10.1021/acsmedchemlett.0c00220] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
13 Allouche EMD, Al-Saleh A, Charette AB. Iron-catalyzed synthesis of cyclopropanes by in situ generation and decomposition of electronically diversified diazo compounds. Chem Commun (Camb) 2018;54:13256-9. [PMID: 30411744 DOI: 10.1039/c8cc07060a] [Cited by in Crossref: 15] [Cited by in F6Publishing: 3] [Article Influence: 3.8] [Reference Citation Analysis]
14 Gutiérrez-Bonet Á, Popov S, Emmert MH, Hughes JME, Nolting AF, Ruccolo S, Wang Y. Asymmetric Synthesis of Tertiary and Secondary Cyclopropyl Boronates via Cyclopropanation of Enantioenriched Alkenyl Boronic Esters. Org Lett 2022. [PMID: 35544734 DOI: 10.1021/acs.orglett.2c01018] [Reference Citation Analysis]
15 Kumar V, Moritz AE, Keck TM, Bonifazi A, Ellenberger MP, Sibley CD, Free RB, Shi L, Lane JR, Sibley DR, Newman AH. Synthesis and Pharmacological Characterization of Novel trans-Cyclopropylmethyl-Linked Bivalent Ligands That Exhibit Selectivity and Allosteric Pharmacology at the Dopamine D3 Receptor (D3R). J Med Chem 2017;60:1478-94. [PMID: 28186762 DOI: 10.1021/acs.jmedchem.6b01688] [Cited by in Crossref: 33] [Cited by in F6Publishing: 31] [Article Influence: 6.6] [Reference Citation Analysis]
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17 Liu S, Qian H, Zhang T, Xie H, Han Z, Guo W, Huang H, Sun J. Mild Intermolecular Synthesis of a Cyclopropane-Containing Tricyclic Skeleton: Unusual Reactivity of Isobenzopyryliums. Angew Chem Int Ed Engl 2021;60:21272-6. [PMID: 34342934 DOI: 10.1002/anie.202108258] [Reference Citation Analysis]
18 Biernasiuk A, Berecka-Rycerz A, Gumieniczek A, Malm M, Łączkowski KZ, Szymańska J, Malm A. The newly synthesized thiazole derivatives as potential antifungal compounds against Candida albicans. Appl Microbiol Biotechnol 2021;105:6355-67. [PMID: 34410437 DOI: 10.1007/s00253-021-11477-7] [Reference Citation Analysis]
19 Sun X, Gu P, Qin J, Su Y. Rhodium-catalysed diastereo- and enantio-selective cyclopropanation of α-boryl styrenes. Chem Commun (Camb) 2020;56:12379-82. [PMID: 32930681 DOI: 10.1039/d0cc02549f] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.5] [Reference Citation Analysis]
20 Wen Z, Salmaso V, Jung YH, Phung NB, Gopinatth V, Shah Q, Patterson AT, Randle JCR, Chen Z, Salvemini D, Lieberman DI, Whitehead GS, Karcz TP, Cook DN, Jacobson KA. Bridged Piperidine Analogues of a High Affinity Naphthalene-Based P2Y14R Antagonist. J Med Chem 2022. [PMID: 35113556 DOI: 10.1021/acs.jmedchem.1c01964] [Reference Citation Analysis]
21 Chang H, Zheng W, Zheng Y, Zhu D, Wang J. The DFT study on Rh–C bond dissociation enthalpies of (iminoacyl)rhodium(III)hydride and (iminoacyl)rhodium(III)alkyl. Tetrahedron Letters 2019;60:310-21. [DOI: 10.1016/j.tetlet.2018.12.042] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
22 Ayub R, Papadakis R, Jorner K, Zietz B, Ottosson H. Cyclopropyl Group: An Excited-State Aromaticity Indicator? Chemistry 2017;23:13684-95. [PMID: 28683165 DOI: 10.1002/chem.201701404] [Cited by in Crossref: 7] [Cited by in F6Publishing: 3] [Article Influence: 1.4] [Reference Citation Analysis]
23 Fu X, Tang J, Hua R, Li X, Kang Z, Qiu H, Hu W. Functionalization of DNA-Tagged Alkenes with Diazo Compounds via Photocatalysis. Org Lett 2022. [PMID: 35289626 DOI: 10.1021/acs.orglett.2c00516] [Reference Citation Analysis]
24 Carminati DM, Fasan R. Stereoselective Cyclopropanation of Electron-Deficient Olefins with a Cofactor Redesigned Carbene Transferase Featuring Radical Reactivity. ACS Catal 2019;9:9683-97. [PMID: 32257582 DOI: 10.1021/acscatal.9b02272] [Cited by in Crossref: 35] [Cited by in F6Publishing: 25] [Article Influence: 11.7] [Reference Citation Analysis]
25 Mitchell ML, Xu L, Newby ZE, Desai MC. Synthesis of novel HIV-1 protease inhibitors via diastereoselective Henry reaction with nitrocyclopropane. Tetrahedron Letters 2017;58:1123-6. [DOI: 10.1016/j.tetlet.2017.01.104] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 0.6] [Reference Citation Analysis]
26 Carminati DM, Moore EJ, Fasan R. Strategies for the expression and characterization of artificial myoglobin-based carbene transferases. Methods Enzymol 2020;644:35-61. [PMID: 32943150 DOI: 10.1016/bs.mie.2020.07.007] [Reference Citation Analysis]
27 Mayer C, Ladd CL, Charette AB. Utilization of BozPhos as an Effective Ligand in Enantioselective C-H Functionalization of Cyclopropanes: Synthesis of Dihydroisoquinolones and Dihydroquinolones. Org Lett 2019;21:2639-44. [PMID: 30924670 DOI: 10.1021/acs.orglett.9b00627] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
28 Ladd CL, Charette AB. Access to Cyclopropyl-Fused Azacycles via a Palladium-Catalyzed Direct Alkenylation Strategy. Org Lett 2016;18:6046-9. [PMID: 27934342 DOI: 10.1021/acs.orglett.6b02982] [Cited by in Crossref: 25] [Cited by in F6Publishing: 18] [Article Influence: 4.2] [Reference Citation Analysis]
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30 Pirovano V, Brambilla E, Tseberlidis G. [Copper(I)(Pyridine-Containing Ligand)] Catalyzed Regio- and Steroselective Synthesis of 2-Vinylcyclopropa[ b ]indolines from 2-Vinylindoles. Org Lett 2018;20:405-8. [DOI: 10.1021/acs.orglett.7b03704] [Cited by in Crossref: 19] [Cited by in F6Publishing: 10] [Article Influence: 4.8] [Reference Citation Analysis]
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33 Ercan S, Çınar E, Özaydın C, Efe Ertürk N, Çakmak R. Inhibitor design for 3‐hydroxy‐3‐methyl‐glutaryl‐CoA reductase enzyme; molecular docking and determination of molecular and electronic properties of ligands by density functional theory method. J Heterocyclic Chem 2020;57:2875-88. [DOI: 10.1002/jhet.3996] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
34 Zhang J, Jin H, Sun J, Wang J, Zhao L. Time-Economical Synthesis of Bis-Spiro Cyclopropanes via Cascade 1,6-Conjugate Addition/Dearomatization Reaction of para -Quinone Methides with 3-Chlorooxindoles: Time-Economical Synthesis of Bis-Spiro Cyclopropanes via Cascade 1,6-Conjugate Addition/Dearomatization Reaction of para-Quinone Methides with 3-Chlor. Eur J Org Chem 2020;2020:4988-94. [DOI: 10.1002/ejoc.202000830] [Cited by in Crossref: 11] [Cited by in F6Publishing: 3] [Article Influence: 5.5] [Reference Citation Analysis]
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36 Jerhaoui S, Chahdoura F, Rose C, Djukic J, Wencel-delord J, Colobert F. Enantiopure Sulfinyl Aniline as a Removable and Recyclable Chiral Auxiliary for Asymmetric C(sp 3 )−H Bond Activation. Chem Eur J 2016;22:17397-406. [DOI: 10.1002/chem.201603507] [Cited by in Crossref: 36] [Cited by in F6Publishing: 29] [Article Influence: 6.0] [Reference Citation Analysis]
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42 Jerhaoui S, Djukic J, Wencel-delord J, Colobert F. Asymmetric, Nearly Barrierless C(sp 3 )–H Activation Promoted by Easily-Accessible N- Protected Aminosulfoxides as New Chiral Ligands. ACS Catal 2019;9:2532-42. [DOI: 10.1021/acscatal.8b04946] [Cited by in Crossref: 25] [Cited by in F6Publishing: 7] [Article Influence: 8.3] [Reference Citation Analysis]
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45 Wu Y, Cao S, Douair I, Maron L, Bi X. Computational Insights into Different Mechanisms for Ag-, Cu-, and Pd-Catalyzed Cyclopropanation of Alkenes and Sulfonyl Hydrazones. Chemistry 2021;27:5999-6006. [PMID: 33443293 DOI: 10.1002/chem.202005193] [Cited by in Crossref: 4] [Article Influence: 4.0] [Reference Citation Analysis]
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48 Carreras J, Caballero A, Pérez PJ. Enantio- and Diastereoselective Cyclopropanation of 1-Alkenylboronates: Synthesis of 1-Boryl-2,3-Disubstituted Cyclopropanes. Angew Chem 2018;130:2358-62. [DOI: 10.1002/ange.201710415] [Cited by in Crossref: 9] [Cited by in F6Publishing: 6] [Article Influence: 2.3] [Reference Citation Analysis]
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54 Spencer JA, Jamieson C, Talbot EPA. One-Pot, Three-Step Synthesis of Cyclopropylboronic Acid Pinacol Esters from Synthetically Tractable Propargylic Silyl Ethers. Org Lett 2017;19:3891-4. [DOI: 10.1021/acs.orglett.7b01778] [Cited by in Crossref: 14] [Cited by in F6Publishing: 10] [Article Influence: 2.8] [Reference Citation Analysis]
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