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For: 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]
Number Citing Articles
1 Zhai S, Qiu S, Yang S, Gao X, Feng X, Yun C, Han N, Niu Y, Wang J, Zhai H. Facile access to β-hydroxyl ketones via a cobalt-catalyzed ring-opening/hydroxylation cascade of cyclopropanols. Chinese Chemical Letters 2022. [DOI: 10.1016/j.cclet.2022.06.080] [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 Xu L, Shi H. Cobalt-catalyzed divergent functionalization of N-sulfonyl amines via β-carbon elimination. Sci China Chem . [DOI: 10.1007/s11426-022-1251-4] [Reference Citation Analysis]
4 Yan H, Smith GS, Chen F. Recent advances using cyclopropanols and cyclobutanols in ring-opening asymmetric synthesis. Green Synthesis and Catalysis 2022. [DOI: 10.1016/j.gresc.2022.05.007] [Reference Citation Analysis]
5 Kitabayashi A, Mizushima S, Higashida K, Yasuda Y, Shimizu Y, Sawamura M. Insights into the Mechanism of Enantioselective Copper‐Catalyzed Ring‐Opening Allylic Alkylation of Cyclopropanols. Adv Synth Catal 2022;364:1855-62. [DOI: 10.1002/adsc.202200157] [Reference Citation Analysis]
6 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]
7 Pati BV, Ghosh A, Yadav K, Banjare SK, Pandey S, Lourderaj U, Ravikumar PC. Palladium-catalyzed selective C-C bond cleavage and stereoselective alkenylation between cyclopropanol and 1,3-diyne: one-step synthesis of diverse conjugated enynes. Chem Sci 2022;13:2692-700. [PMID: 35340856 DOI: 10.1039/d1sc04780a] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 4.0] [Reference Citation Analysis]
8 Zhou G, Shen X. Synthesis of Cyclopropenols Enabled by Visible-Light-Induced Organocatalyzed [2+1] Cyclization. Angew Chem Int Ed Engl 2022;61:e202115334. [PMID: 34994996 DOI: 10.1002/anie.202115334] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 6.0] [Reference Citation Analysis]
9 Sekiguchi Y, Yoshikai N. Zinc-Mediated Hydroxyallylation of Aldehydes with Cyclopropanols: Direct Access to Vicinal anti-sec,tert-Diols via Enolized Homoenolates. Org Lett 2022. [PMID: 35030003 DOI: 10.1021/acs.orglett.1c04331] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
10 Xu H, Fang X, Huang W, Xu Z, Li L, Ye F, Cao J, Xu L. Catalytic regio- and stereoselective silicon–carbon bond formations on unsymmetric gem -difluorocyclopropenes by capture of silyl metal species. Org Chem Front . [DOI: 10.1039/d2qo00943a] [Reference Citation Analysis]
11 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]
12 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]
13 Zhang Q, Zhou SW, Shi CY, Yin L. Catalytic Asymmetric Allylic Substitution with Copper(I) Homoenolates Generated from Cyclopropanols. Angew Chem Int Ed Engl 2021;60:26351-6. [PMID: 34617380 DOI: 10.1002/anie.202110709] [Cited by in Crossref: 2] [Cited by in F6Publishing: 6] [Article Influence: 2.0] [Reference Citation Analysis]
14 Sekiguchi Y, Yoshikai N. Zinc-Catalyzed β-Functionalization of Cyclopropanols via Enolized Homoenolate. J Am Chem Soc 2021;143:18400-5. [PMID: 34714060 DOI: 10.1021/jacs.1c10109] [Reference Citation Analysis]
15 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]
16 Liang Z, Chong Q, Meng F. Cobalt-catalyzed atom-economical, diastereo- and enantioselective coupling of aldimines and cyclopropanols. Sci China Chem 2021;64:1750-5. [DOI: 10.1007/s11426-021-1062-y] [Cited by in Crossref: 1] [Cited by in F6Publishing: 5] [Article Influence: 1.0] [Reference Citation Analysis]
17 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]
18 Hu Y, Zhang Z, Liu Y, Zhang W. Cobalt-Catalyzed Chemo- and Enantioselective Hydrogenation of Conjugated Enynes. Angew Chem Int Ed Engl 2021;60:16989-93. [PMID: 34062038 DOI: 10.1002/anie.202106566] [Cited by in F6Publishing: 12] [Reference Citation Analysis]
19 Hu Y, Zhang Z, Liu Y, Zhang W. Cobalt‐Catalyzed Chemo‐ and Enantioselective Hydrogenation of Conjugated Enynes. Angew Chem 2021;133:17126-30. [DOI: 10.1002/ange.202106566] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
20 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]
21 Sekiguchi Y, Yoshikai N. Enantioselective Conjugate Addition of Catalytically Generated Zinc Homoenolate. J Am Chem Soc 2021;143:4775-81. [PMID: 33724809 DOI: 10.1021/jacs.1c00869] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 4.0] [Reference Citation Analysis]