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For: 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: 34] [Article Influence: 9.3] [Reference Citation Analysis]
Number Citing Articles
1 Cohen Y, Marek I. Regio- and Diastereoselective Carbometalation Reaction of Cyclopropenes. Acc Chem Res . [DOI: 10.1021/acs.accounts.2c00424] [Reference Citation Analysis]
2 Wang L, Lu W, Zhang J, Chong Q, Meng F. Cobalt‐Catalyzed Regio‐, Diastereo‐ and Enantioselective Intermolecular Hydrosilylation of 1,3‐Dienes with Prochiral Silanes. Angewandte Chemie. [DOI: 10.1002/ange.202205624] [Reference Citation Analysis]
3 Patel K, Lanke V, Marek I. Stereospecific Construction of Quaternary Carbon Stereocenters from Quaternary Carbon Stereocenters. J Am Chem Soc 2022. [PMID: 35412821 DOI: 10.1021/jacs.2c01695] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
4 Lu W, Zhao Y, Meng F. Cobalt-Catalyzed Sequential Site- and Stereoselective Hydrosilylation of 1,3- and 1,4-Enynes. J Am Chem Soc 2022. [PMID: 35298144 DOI: 10.1021/jacs.2c00288] [Cited by in Crossref: 10] [Cited by in F6Publishing: 4] [Article Influence: 10.0] [Reference Citation Analysis]
5 Zhu D, Zhao Y, Chong Q, Meng F. Cobalt‐Catalyzed Enantioselec tive Ring‐Opening Reactions of Oxa‐ and Aza‐bicyclic Alkenes with Alkenylboronic Acids. Chin J Chem 2022;40:190-4. [DOI: 10.1002/cjoc.202100622] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
6 Cohen Y, Marek I. Directed Regioselective Carbometallation of 1,2-Dialkyl-Substituted Cyclopropenes. Angew Chem Int Ed Engl 2021;60:26368-72. [PMID: 34617656 DOI: 10.1002/anie.202111382] [Cited by in F6Publishing: 8] [Reference Citation Analysis]
7 Cohen Y, Marek I. Directed Regioselective Carbometallation of 1,2‐Dialkyl‐Substituted Cyclopropenes. Angew Chem 2021;133:26572-6. [DOI: 10.1002/ange.202111382] [Cited by in Crossref: 4] [Cited by in F6Publishing: 1] [Article Influence: 4.0] [Reference Citation Analysis]
8 Wang L, Wang L, Li M, Chong Q, Meng F. Cobalt-Catalyzed Diastereo- and Enantioselective Reductive Allyl Additions to Aldehydes with Allylic Alcohol Derivatives via Allyl Radical Intermediates. J Am Chem Soc 2021;143:12755-65. [PMID: 34352174 DOI: 10.1021/jacs.1c05690] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
9 Li YL, Zhang SQ, Chen J, Xia JB. Highly Regio- and Enantioselective Reductive Coupling of Alkynes and Aldehydes via Photoredox Cobalt Dual Catalysis. J Am Chem Soc 2021;143:7306-13. [PMID: 33951915 DOI: 10.1021/jacs.1c03527] [Cited by in Crossref: 7] [Article Influence: 7.0] [Reference Citation Analysis]
10 Zhang H, Huang J, Meng F. Cobalt-catalyzed diastereo- and enantioselective allyl addition to aldehydes and α-ketoesters through allylic C–H functionalization. Cell Reports Physical Science 2021;2:100406. [DOI: 10.1016/j.xcrp.2021.100406] [Cited by in Crossref: 6] [Cited by in F6Publishing: 4] [Article Influence: 6.0] [Reference Citation Analysis]
11 Nie S, Lu A, Kuker EL, Dong VM. Enantioselective Hydrothiolation: Diverging Cyclopropenes through Ligand Control. J Am Chem Soc 2021;143:6176-84. [PMID: 33856804 DOI: 10.1021/jacs.1c00939] [Cited by in Crossref: 3] [Article Influence: 3.0] [Reference Citation Analysis]
12 Schuppe AW, Knippel JL, Borrajo-Calleja GM, Buchwald SL. Enantioselective Hydroalkenylation of Olefins with Enol Sulfonates Enabled by Dual Copper Hydride and Palladium Catalysis. J Am Chem Soc 2021;143:5330-5. [PMID: 33784090 DOI: 10.1021/jacs.1c02117] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
13 Muriel B, Waser J. Azide Radical Initiated Ring Opening of Cyclopropenes Leading to Alkenyl Nitriles and Polycyclic Aromatic Compounds. Angew Chem Int Ed Engl 2021;60:4075-9. [PMID: 33205851 DOI: 10.1002/anie.202013516] [Cited by in Crossref: 3] [Cited by in F6Publishing: 5] [Article Influence: 3.0] [Reference Citation Analysis]
14 Muriel B, Waser J. Azide Radical Initiated Ring Opening of Cyclopropenes Leading to Alkenyl Nitriles and Polycyclic Aromatic Compounds. Angew Chem 2021;133:4121-5. [DOI: 10.1002/ange.202013516] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
15 Wu L, Wei H, Shen J, Chen J, Zhang W. Development of Earth-Abundant Metals-Catalyzed Enantioselective Alkenylations Using Alkenyl Metal Reagents. Acta Chimica Sinica 2021;79:1331. [DOI: 10.6023/a21070338] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
16 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: 21] [Article Influence: 3.5] [Reference Citation Analysis]
17 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: 8] [Article Influence: 1.0] [Reference Citation Analysis]
18 Pierrot D, Marek I. Stereospecific Reactions Leading to Allylboronic Esters Within Acyclic Systems Bearing Distant Stereocenters. Angew Chem Int Ed Engl 2020;59:20434-8. [PMID: 32757448 DOI: 10.1002/anie.202010135] [Cited by in Crossref: 1] [Cited by in F6Publishing: 3] [Article Influence: 0.5] [Reference Citation Analysis]
19 Zhang Y, Li Y, Zhou W, Zhang M, Zhang Q, Jia R, Zhao J. Assembly of polysubstituted chiral cyclopropylamines via highly enantioselective Cu-catalyzed three-component cyclopropene alkenylamination. Chem Commun (Camb) 2020;56:12250-3. [PMID: 32929423 DOI: 10.1039/d0cc01060j] [Cited by in Crossref: 2] [Article Influence: 1.0] [Reference Citation Analysis]
20 Wang D, He Y, Dai H, Huang C, Yuan X, Xie J. Manganese‐Catalyzed Hydrocarbofunctionalization of Internal Alkenes . Chin J Chem 2020;38:1497-502. [DOI: 10.1002/cjoc.202000376] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
21 Lanke V, Marek I. Stereospecific nucleophilic substitution at tertiary and quaternary stereocentres. Chem Sci 2020;11:9378-85. [PMID: 34094203 DOI: 10.1039/d0sc02562c] [Cited by in Crossref: 5] [Article Influence: 2.5] [Reference Citation Analysis]
22 Prasad Raiguru B, Nayak S, Ranjan Mishra D, Das T, Mohapatra S, Priyadarsini Mishra N. Synthetic Applications of Cyclopropene and Cyclopropenone: Recent Progress and Developments. Asian J Org Chem 2020;9:1088-132. [DOI: 10.1002/ajoc.202000193] [Cited by in Crossref: 12] [Cited by in F6Publishing: 13] [Article Influence: 6.0] [Reference Citation Analysis]
23 Dian L, Marek I. Cobalt-Catalyzed Diastereoselective and Enantioselective Hydrosilylation of Achiral Cyclopropenes. Org Lett 2020;22:4914-8. [PMID: 32506912 DOI: 10.1021/acs.orglett.0c01833] [Cited by in Crossref: 9] [Article Influence: 4.5] [Reference Citation Analysis]
24 Cohen A, Chagneau J, Marek I. Stereoselective Preparation of Distant Stereocenters (1,5) within Acyclic Molecules. ACS Catal 2020;10:7154-61. [DOI: 10.1021/acscatal.0c01762] [Cited by in Crossref: 14] [Cited by in F6Publishing: 5] [Article Influence: 7.0] [Reference Citation Analysis]
25 Wang D, Dong J, Fan W, Yuan XA, Han J, Xie J. Dimeric Manganese-Catalyzed Hydroarylation and Hydroalkenylation of Unsaturated Amides. Angew Chem Int Ed Engl 2020;59:8430-4. [PMID: 32129534 DOI: 10.1002/anie.201916305] [Cited by in Crossref: 13] [Cited by in F6Publishing: 15] [Article Influence: 6.5] [Reference Citation Analysis]
26 Wang D, Dong J, Fan W, Yuan X, Han J, Xie J. Dimeric Manganese‐Catalyzed Hydroarylation and Hydroalkenylation of Unsaturated Amides. Angew Chem 2020;132:8508-12. [DOI: 10.1002/ange.201916305] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
27 Liu X, Liu B, Liu Q. Migratory Hydrogenation of Terminal Alkynes by Base/Cobalt Relay Catalysis. Angew Chem Int Ed Engl 2020;59:6750-5. [PMID: 32118345 DOI: 10.1002/anie.201916014] [Cited by in Crossref: 7] [Cited by in F6Publishing: 10] [Article Influence: 3.5] [Reference Citation Analysis]
28 Zheng G, Zhou Z, Zhu G, Zhai S, Xu H, Duan X, Yi W, Li X. Rhodium(III)‐Catalyzed Enantio‐ and Diastereoselective C−H Cyclopropylation of N‐Phenoxylsulfonamides: Combined Experimental and Computational Studies. Angew Chem Int Ed 2020;59:2890-6. [DOI: 10.1002/anie.201913794] [Cited by in Crossref: 42] [Cited by in F6Publishing: 51] [Article Influence: 21.0] [Reference Citation Analysis]
29 Dian L, Marek I. Pd-Catalyzed Enantioselective Hydroalkynylation of Cyclopropenes. ACS Catal 2020;10:1289-93. [PMID: 32953232 DOI: 10.1021/acscatal.9b04960] [Cited by in Crossref: 23] [Cited by in F6Publishing: 14] [Article Influence: 11.5] [Reference Citation Analysis]
30 Zheng G, Zhou Z, Zhu G, Zhai S, Xu H, Duan X, Yi W, Li X. Rhodium(III)‐Catalyzed Enantio‐ and Diastereoselective C−H Cyclopropylation of N‐Phenoxylsulfonamides: Combined Experimental and Computational Studies. Angew Chem 2020;132:2912-8. [DOI: 10.1002/ange.201913794] [Cited by in Crossref: 16] [Cited by in F6Publishing: 15] [Article Influence: 8.0] [Reference Citation Analysis]
31 Wang H, Zhang G, Zhang Q, Wang Y, Li Y, Xiong T, Zhang Q. Copper-catalyzed non-directed hydrosilylation of cyclopropenes: highly diastereoselective synthesis of fully substituted cyclopropylsilanes. Chem Commun 2020;56:1819-22. [DOI: 10.1039/c9cc09584e] [Cited by in Crossref: 8] [Cited by in F6Publishing: 12] [Article Influence: 4.0] [Reference Citation Analysis]
32 Liu J, Yao H, Li X, Wu H, Lin A, Yao H, Xu J, Xu S. Organocatalytic 1,5-trifluoromethylthio-sulfonylation of vinylcyclopropane mediated by visible light in the water phase. Org Chem Front 2020;7:1314-20. [DOI: 10.1039/d0qo00343c] [Cited by in Crossref: 6] [Article Influence: 3.0] [Reference Citation Analysis]
33 Li P, Zhang X, Shi M. Recent developments in cyclopropene chemistry. Chem Commun 2020;56:5457-71. [DOI: 10.1039/d0cc01612h] [Cited by in Crossref: 20] [Article Influence: 10.0] [Reference Citation Analysis]
34 Zhang Z, Meng X, Sheng J, Lan Q, Wang X. Enantioselective Copper-Catalyzed 1,5-Cyanotrifluoromethylation of Vinylcyclopropanes. Org Lett 2019;21:8256-60. [DOI: 10.1021/acs.orglett.9b03012] [Cited by in Crossref: 16] [Cited by in F6Publishing: 9] [Article Influence: 5.3] [Reference Citation Analysis]