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For: Montesinos-Magraner M, Costantini M, Ramírez-Contreras R, Muratore ME, Johansson MJ, Mendoza A. General Cyclopropane Assembly by Enantioselective Transfer of a Redox-Active Carbene to Aliphatic Olefins. Angew Chem Int Ed Engl 2019;58:5930-5. [PMID: 30675970 DOI: 10.1002/anie.201814123] [Cited by in Crossref: 28] [Cited by in F6Publishing: 19] [Article Influence: 9.3] [Reference Citation Analysis]
Number Citing Articles
1 Shi X, Li S, Wu L. H 2 ‐Acceptorless Dehydrogenative Boration and Transfer Boration of Alkenes Enabled by Zirconium Catalyst. Angew Chem 2019;131:16313-7. [DOI: 10.1002/ange.201908931] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 1.7] [Reference Citation Analysis]
2 Hryschuk OV, Yurov Y, Tymtsunik AV, Kovtunenko VO, Komarov IV, Grygorenko OO. Multigram Synthesis and C−C/C−N Couplings of Functionalized 1,2‐Disubstituted Cyclopropyltrifluoroborates. Adv Synth Catal 2019;361:5428-39. [DOI: 10.1002/adsc.201900879] [Cited by in Crossref: 9] [Article Influence: 3.0] [Reference Citation Analysis]
3 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]
4 Mato M, Franchino A, Garcı A-Morales C, Echavarren AM. Gold-Catalyzed Synthesis of Small Rings. Chem Rev 2021;121:8613-84. [PMID: 33136374 DOI: 10.1021/acs.chemrev.0c00697] [Cited by in Crossref: 16] [Cited by in F6Publishing: 6] [Article Influence: 8.0] [Reference Citation Analysis]
5 Konik YA, Kananovich DG. Asymmetric synthesis with titanacyclopropane reagents: From early results to the recent achievements. Tetrahedron Letters 2020;61:152036. [DOI: 10.1016/j.tetlet.2020.152036] [Cited by in Crossref: 2] [Article Influence: 1.0] [Reference Citation Analysis]
6 Chowdhury R, Mendoza A. N-Hydroxyphthalimidyl diazoacetate (NHPI-DA): a modular methylene linchpin for the C-H alkylation of indoles. Chem Commun (Camb) 2021;57:4532-5. [PMID: 33956022 DOI: 10.1039/d1cc01026c] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
7 Zhao C, Feng Z, Xu G, Gao A, Chen J, Wang Z, Xu P. Highly Enantioselective Construction of Strained Spiro[2,3]hexanes through a Michael Addition/Ring Expansion/Cyclization Cascade. Angew Chem 2020;132:3082-6. [DOI: 10.1002/ange.201912834] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.5] [Reference Citation Analysis]
8 Zhang Y, Zhou G, Gong X, Guo Z, Qi X, Shen X. Diastereoselective Transfer of Tri(di)fluoroacetylsilanes‐Derived Carbenes to Alkenes. Angewandte Chemie. [DOI: 10.1002/ange.202202175] [Reference Citation Analysis]
9 Mato M, Montesinos-Magraner M, Sugranyes AR, Echavarren AM. Rh(II)-Catalyzed Alkynylcyclopropanation of Alkenes by Decarbenation of Alkynylcycloheptatrienes. J Am Chem Soc 2021;143:10760-9. [PMID: 34236835 DOI: 10.1021/jacs.1c05422] [Reference Citation Analysis]
10 Zubrytski DM, Elek GZ, Lopp M, Kananovich DG. Generation of Mixed Anhydrides via Oxidative Fragmentation of Tertiary Cyclopropanols with Phenyliodine(III) Dicarboxylates. Molecules 2020;26:E140. [PMID: 33396847 DOI: 10.3390/molecules26010140] [Reference Citation Analysis]
11 Guo JY, Zhang ZY, Guan T, Mao LW, Ban Q, Zhao K, Loh TP. Photoredox-catalyzed stereoselective alkylation of enamides with N-hydroxyphthalimide esters via decarboxylative cross-coupling reactions. Chem Sci 2019;10:8792-8. [PMID: 31803451 DOI: 10.1039/c9sc03070k] [Cited by in Crossref: 28] [Article Influence: 9.3] [Reference Citation Analysis]
12 Pons A, Decaens J, Najjar R, Otog N, Arribat M, Jolly S, Couve-Bonnaire S, Sebban M, Coadou G, Oulyadi H, Speybrouck D, Iwasa S, Charette AB, Poisson T, Jubault P. Fluorocyclopropane-Containing Proline Analogue: Synthesis and Conformation of an Item in the Peptide Chemist's Toolbox. ACS Omega 2022;7:4868-78. [PMID: 35187307 DOI: 10.1021/acsomega.1c05337] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
13 Elek GZ, Koppel K, Zubrytski DM, Konrad N, Järving I, Lopp M, Kananovich DG. Divergent Access to Histone Deacetylase Inhibitory Cyclopeptides via a Late-Stage Cyclopropane Ring Cleavage Strategy. Short Synthesis of Chlamydocin. Org Lett 2019;21:8473-8. [PMID: 31596600 DOI: 10.1021/acs.orglett.9b03305] [Cited by in Crossref: 8] [Cited by in F6Publishing: 5] [Article Influence: 2.7] [Reference Citation Analysis]
14 Zhang H, Huang W, Wang T, Meng F. Cobalt‐Catalyzed Diastereo‐ and Enantioselective Hydroalkenylation of Cyclopropenes with Alkenylboronic Acids. Angew Chem Int Ed 2019;58:11049-53. [DOI: 10.1002/anie.201904994] [Cited by in Crossref: 28] [Cited by in F6Publishing: 16] [Article Influence: 9.3] [Reference Citation Analysis]
15 Huang W, Meng F. Cobalt‐Catalyzed Diastereo‐ and Enantioselective Hydroalkylation of Cyclopropenes with Cobalt Homoenolates. Angew Chem Int Ed 2021;60:2694-8. [DOI: 10.1002/anie.202012122] [Cited by in Crossref: 7] [Cited by in F6Publishing: 4] [Article Influence: 3.5] [Reference Citation Analysis]
16 Zhang L, Oestreich M. Copper-Catalyzed Enantio- and Diastereoselective Addition of Silicon Nucleophiles to 3,3-Disubstituted Cyclopropenes. Chemistry 2019;25:14304-7. [PMID: 31531992 DOI: 10.1002/chem.201904272] [Cited by in Crossref: 12] [Article Influence: 4.0] [Reference Citation Analysis]
17 Herraiz AG, Suero MG. A transition-metal-free & diazo-free styrene cyclopropanation. Chem Sci 2019;10:9374-9. [PMID: 32110302 DOI: 10.1039/c9sc02749a] [Cited by in Crossref: 6] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
18 Planas F, Costantini M, Montesinos-Magraner M, Himo F, Mendoza A. Combined Experimental and Computational Study of Ruthenium N-Hydroxyphthalimidoyl Carbenes in Alkene Cyclopropanation Reactions. ACS Catal 2021;11:10950-63. [PMID: 34504736 DOI: 10.1021/acscatal.1c02540] [Reference Citation Analysis]
19 Zhang H, Huang W, Wang T, Meng F. Cobalt‐Catalyzed Diastereo‐ and Enantioselective Hydroalkenylation of Cyclopropenes with Alkenylboronic Acids. Angew Chem 2019;131:11165-9. [DOI: 10.1002/ange.201904994] [Cited by in Crossref: 12] [Cited by in F6Publishing: 8] [Article Influence: 4.0] [Reference Citation Analysis]
20 Harada S, Yanagawa M, Nemoto T. Dual-Functional Enone-Directing Group/Electrophile for Sequential C–C Bond Formation with α-Diazomalonates: A Short Synthesis of Chiral 3,4-Fused Tricyclic Indoles. ACS Catal 2020;10:11971-9. [DOI: 10.1021/acscatal.0c03940] [Cited by in Crossref: 17] [Cited by in F6Publishing: 9] [Article Influence: 8.5] [Reference Citation Analysis]
21 Huang W, Meng F. Cobalt‐Catalyzed Diastereo‐ and Enantioselective Hydroalkylation of Cyclopropenes with Cobalt Homoenolates. Angew Chem 2021;133:2726-30. [DOI: 10.1002/ange.202012122] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
22 Neouchy Z, Verhoeven J, Kong H, Zhao Y, Wang W, Brambilla M, Van Hecke K, Meerpoel L, Thuring JW, Verniest G, Winne J. Stereodivergent Synthesis of Biologically Active Spironucleoside Scaffolds via Catalytic Cyclopropanation of 4-exo-Methylene Furanosides. J Org Chem 2021;86:17344-61. [PMID: 34748342 DOI: 10.1021/acs.joc.1c01611] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
23 Otog N, Inoue H, Trinh DTT, Batgerel Z, Langendorf NM, Fujisawa I, Iwasa S. Ru(II)‐Pheox Catalyzed Highly Stereoselective Cyclopropanation of Allyl‐ and Vinylsilanes with Diazoesters and Their Synthetic Applications. ChemCatChem 2021;13:328-37. [DOI: 10.1002/cctc.202001427] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
24 Chan CM, Xing Q, Chow YC, Hung SF, Yu WY. Photoredox Decarboxylative C(sp3)-N Coupling of α-Diazoacetates with Alkyl N-Hydroxyphthalimide Esters for Diversified Synthesis of Functionalized N-Alkyl Hydrazones. Org Lett 2019;21:8037-43. [PMID: 31524416 DOI: 10.1021/acs.orglett.9b03020] [Cited by in Crossref: 13] [Cited by in F6Publishing: 7] [Article Influence: 4.3] [Reference Citation Analysis]
25 Yu Z, Mendoza A. Enantioselective Assembly of Congested Cyclopropanes using Redox-Active Aryldiazoacetates. ACS Catal 2019;9:7870-5. [DOI: 10.1021/acscatal.9b02615] [Cited by in Crossref: 22] [Cited by in F6Publishing: 11] [Article Influence: 7.3] [Reference Citation Analysis]
26 He Y, Huang Z, Wu K, Ma J, Zhou YG, Yu Z. Recent advances in transition-metal-catalyzed carbene insertion to C-H bonds. Chem Soc Rev 2022. [PMID: 35297455 DOI: 10.1039/d1cs00895a] [Cited by in Crossref: 10] [Cited by in F6Publishing: 7] [Article Influence: 10.0] [Reference Citation Analysis]
27 Zhao C, Feng Z, Xu G, Gao A, Chen J, Wang Z, Xu P. Highly Enantioselective Construction of Strained Spiro[2,3]hexanes through a Michael Addition/Ring Expansion/Cyclization Cascade. Angew Chem Int Ed 2020;59:3058-62. [DOI: 10.1002/anie.201912834] [Cited by in Crossref: 12] [Cited by in F6Publishing: 5] [Article Influence: 6.0] [Reference Citation Analysis]
28 Trifonova EA, Ankudinov NM, Chusov DA, Nelyubina YV, Perekalin DS. Asymmetric cyclopropanation of electron-rich alkenes by the racemic diene rhodium catalyst: the chiral poisoning approach. Chem Commun (Camb) 2022;58:6709-12. [PMID: 35593764 DOI: 10.1039/d2cc01648f] [Reference Citation Analysis]
29 Zhang Y, Zhou G, Gong X, Guo Z, Qi X, Shen X. Diastereoselective Transfer of Tri(di)fluoroacetylsilanes-Derived Carbenes to Alkenes. Angew Chem Int Ed Engl 2022;61:e202202175. [PMID: 35415937 DOI: 10.1002/anie.202202175] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
30 Bratt E, Suárez-Pantiga S, Johansson MJ, Mendoza A. Mechanism and regioselectivity of the anionic oxidative rearrangement of 1,3-diketones towards all-carbon quaternary carboxylates. Chem Commun (Camb) 2019;55:8844-7. [PMID: 31169839 DOI: 10.1039/c9cc03331a] [Cited by in Crossref: 7] [Cited by in F6Publishing: 2] [Article Influence: 2.3] [Reference Citation Analysis]
31 Costantini M, Mendoza A. Modular Enantioselective Synthesis of cis-Cyclopropanes through Self-Sensitized Stereoselective Photodecarboxylation with Benzothiazolines. ACS Catal 2021;11:13312-9. [PMID: 34765283 DOI: 10.1021/acscatal.1c03949] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
32 Green SP, Wheelhouse KM, Payne AD, Hallett JP, Miller PW, Bull JA. Thermal Stability and Explosive Hazard Assessment of Diazo Compounds and Diazo Transfer Reagents. Org Process Res Dev 2020;24:67-84. [PMID: 31983869 DOI: 10.1021/acs.oprd.9b00422] [Cited by in Crossref: 41] [Cited by in F6Publishing: 18] [Article Influence: 13.7] [Reference Citation Analysis]
33 Findlay MT, Domingo-Legarda P, McArthur G, Yen A, Larrosa I. Catalysis with cycloruthenated complexes. Chem Sci 2022;13:3335-62. [PMID: 35432864 DOI: 10.1039/d1sc06355c] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
34 Shi X, Li S, Wu L. H 2 ‐Acceptorless Dehydrogenative Boration and Transfer Boration of Alkenes Enabled by Zirconium Catalyst. Angew Chem Int Ed 2019;58:16167-71. [DOI: 10.1002/anie.201908931] [Cited by in Crossref: 11] [Cited by in F6Publishing: 6] [Article Influence: 3.7] [Reference Citation Analysis]
35 Chowdhury R, Yu Z, Tong ML, Kohlhepp SV, Yin X, Mendoza A. Decarboxylative Alkyl Coupling Promoted by NADH and Blue Light. J Am Chem Soc 2020;142:20143-51. [PMID: 33125842 DOI: 10.1021/jacs.0c09678] [Cited by in Crossref: 10] [Cited by in F6Publishing: 4] [Article Influence: 5.0] [Reference Citation Analysis]
36 Caló FP, Zimmer A, Bistoni G, Fürstner A. From Serendipity to Rational Design: Heteroleptic Dirhodium Amidate Complexes for Diastereodivergent Asymmetric Cyclopropanation. J Am Chem Soc 2022. [PMID: 35420801 DOI: 10.1021/jacs.2c02258] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
37 Ma X, Pinto W, Pham LN, Sloman DL, Han Y. Synthetic Studies of 2,2-Difluorobicyclo[1.1.1]pentanes (BCP-F 2 ): The Scope and Limitation of Useful Building Blocks for Medicinal Chemists: Synthetic Studies of 2,2-Difluorobicyclo[1.1.1]pentanes (BCP-F 2 ): The Scope and Limitation of Useful Building Blocks for Medicinal Chemists. Eur J Org Chem 2020;2020:4581-605. [DOI: 10.1002/ejoc.202000679] [Cited by in Crossref: 6] [Cited by in F6Publishing: 4] [Article Influence: 3.0] [Reference Citation Analysis]