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Fanke Meng, Ph.D - Publications

Affiliations: 
2006-2010 Peking University, Beijing, Beijing Shi, China 
 2010-2016 Boston College, Newton, MA, United States 
 2016- SIOC,CAS 
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29 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 Wang L, Lin C, Chong Q, Zhang Z, Meng F. Photoredox cobalt-catalyzed regio-, diastereo- and enantioselective propargylation of aldehydes via propargyl radicals. Nature Communications. 14: 4825. PMID 37563134 DOI: 10.1038/s41467-023-40488-3  0.443
2023 Huang W, Bai J, Guo Y, Chong Q, Meng F. Cobalt-Catalyzed Regiodivergent and Enantioselective Intermolecular Coupling of 1,1-Disubstituted Allenes and Aldehydes. Angewandte Chemie (International Ed. in English). e202219257. PMID 36863999 DOI: 10.1002/anie.202219257  0.438
2023 Liang Z, Wang L, Wang Y, Wang L, Chong Q, Meng F. Cobalt-Catalyzed Diastereo- and Enantioselective Carbon-Carbon Bond Forming Reactions of Cyclobutenes. Journal of the American Chemical Society. PMID 36734874 DOI: 10.1021/jacs.2c12475  0.437
2022 Wang L, Lu W, Zhang J, Chong Q, Meng F. Corrigendum: Cobalt-Catalyzed Regio-, Diastereo- and Enantioselective Intermolecular Hydrosilylation of 1,3-Dienes with Prochiral Silanes. Angewandte Chemie (International Ed. in English). 61: e202213574. PMID 36258266 DOI: 10.1002/anie.202213574  0.534
2022 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 (International Ed. in English). e202205624. PMID 35606326 DOI: 10.1002/anie.202205624  0.33
2022 Lu W, Zhao Y, Meng F. Cobalt-Catalyzed Sequential Site- and Stereoselective Hydrosilylation of 1,3- and 1,4-Enynes. Journal of the American Chemical Society. PMID 35298144 DOI: 10.1021/jacs.2c00288  0.412
2021 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. Journal of the American Chemical Society. PMID 34352174 DOI: 10.1021/jacs.1c05690  0.427
2020 Huang W, Meng F. Cobalt-Catalyzed Diastereo- and Enantioselective Hydroalkylation of Cyclopropenes with Cobalt-Homoenolates. Angewandte Chemie (International Ed. in English). PMID 33052595 DOI: 10.1002/anie.202012122  0.502
2019 Zhang H, Huang W, Wang T, Meng F. Co-Catalyzed Diastereo- and Enantioselective Hydroalkenylation of Cyclopropenes with Alkenylboronic Acids. Angewandte Chemie (International Ed. in English). PMID 31162790 DOI: 10.1002/Anie.201904994  0.513
2018 Li M, Wang J, Meng F. Cu-Catalyzed Enantioselective Reductive Coupling of 1,3-Dienes and Aldimines. Organic Letters. PMID 30403358 DOI: 10.1021/Acs.Orglett.8B03216  0.538
2018 Wen L, Zhang H, Wang J, Meng F. Cu-catalyzed regioselective borylcyanation of 1,3-dienes. Chemical Communications (Cambridge, England). PMID 30371700 DOI: 10.1039/C8Cc07032F  0.533
2018 Chong Q, Zhang S, Cheng F, Wang J, Hong X, Meng F. N-Heterocyclic Carbene-Cu-Catalyzed Enantioselective Allenyl Conjugate Addition. Organic Letters. PMID 30350670 DOI: 10.1021/Acs.Orglett.8B03029  0.579
2018 Cheng F, Lu W, Huang W, Wen L, Li M, Meng F. Cu-catalyzed enantioselective synthesis of tertiary benzylic copper complexes and their addition to carbonyl compounds. Chemical Science. 9: 4992-4998. PMID 29938027 DOI: 10.1039/C8Sc00827B  0.614
2017 Wen L, Yue Z, Zhang H, Chong Q, Meng F. Cu-Catalyzed Enantioselective Boron Addition to N-Heteroaryl-Substituted Alkenes. Organic Letters. 19: 6610-6613. PMID 29172547 DOI: 10.1021/Acs.Orglett.7B03327  0.527
2017 Chong Q, Yue Z, Zhang S, Ji C, Cheng F, Zhang H, Hong X, Meng F. N-heterocyclic Carbene–Cu-Catalyzed Enantioselective Conjugate Additions with Alkenylboronic Esters as Nucleophiles Acs Catalysis. 7: 5693-5698. DOI: 10.1021/Acscatal.7B02132  0.533
2017 Wen L, Cheng F, Li H, Zhang S, Hong X, Meng F. Copper-Catalyzed Enantioselective Hydroboration of 1,1-Disubstituted Alkenes: Method Development, Applications and Mechanistic Studies Asian Journal of Organic Chemistry. 7: 103-106. DOI: 10.1002/Ajoc.201700503  0.577
2016 Meng F, Li X, Torker S, Shi Y, Shen X, Hoveyda AH. Catalytic enantioselective 1,6-conjugate additions of propargyl and allyl groups. Nature. PMID 27479320 DOI: 10.1038/Nature19063  0.729
2016 Li X, Meng F, Torker S, Shi Y, Hoveyda AH. Catalytic Enantioselective Conjugate Additions of (pin)B-Substituted Allylcopper Compounds Generated in situ from Butadiene or Isoprene. Angewandte Chemie (International Ed. in English). PMID 27436785 DOI: 10.1002/Anie.201605001  0.701
2014 Meng F, McGrath KP, Hoveyda AH. Multifunctional organoboron compounds for scalable natural product synthesis. Nature. 513: 367-74. PMID 25230659 DOI: 10.1038/Nature13735  0.743
2014 Meng F, Haeffner F, Hoveyda AH. Diastereo- and enantioselective reactions of bis(pinacolato)diboron, 1,3-enynes, and aldehydes catalyzed by an easily accessible bisphosphine-Cu complex. Journal of the American Chemical Society. 136: 11304-7. PMID 25089917 DOI: 10.1021/Ja5071202  0.713
2013 Meng F, Jang H, Jung B, Hoveyda AH. Cu-catalyzed chemoselective preparation of 2-(pinacolato)boron-substituted allylcopper complexes and their in situ site-, diastereo-, and enantioselective additions to aldehydes and ketones. Angewandte Chemie (International Ed. in English). 52: 5046-51. PMID 23553989 DOI: 10.1002/Anie.201301018  0.736
2013 Meng F, Jung B, Haeffner F, Hoveyda AH. NHC-Cu-catalyzed protoboration of monosubstituted allenes. Ligand-controlled site selectivity, application to synthesis and mechanism. Organic Letters. 15: 1414-7. PMID 23461762 DOI: 10.1021/Ol4004178  0.711
2013 Meng F, Jang H, Hoveyda AH. Exceptionally E- and β-selective NHC-Cu-catalyzed proto-silyl additions to terminal alkynes and site- and enantioselective proto-boryl additions to the resulting vinylsilanes: synthesis of enantiomerically enriched vicinal and geminal borosilanes. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 3204-14. PMID 23325733 DOI: 10.1002/Chem.201203803  0.732
2012 Ren WW, Chen ZX, Xiao Q, Li Y, Sun TW, Zhang ZY, Ye QD, Meng FK, You L, Zhao MZ, Xu LM, Tang YF, Chen JH, Yang Z. Diastereoselective total synthesis of (±)-Schindilactone A, Part 3: The final phase and completion Chemistry - An Asian Journal. 7: 2341-2350. PMID 22761030 DOI: 10.1002/Asia.201200365  0.62
2012 Li Y, Chen ZX, Xiao Q, Ye QD, Sun TW, Meng FK, Ren WW, You L, Xu LM, Wang YF, Chen JH, Yang Z. Diastereoselective total synthesis of (±)-Schindilactone A, Part 2: Construction of the fully functionalized CDEFGH ring system Chemistry - An Asian Journal. 7: 2334-2340. PMID 22761018 DOI: 10.1002/Asia.201200364  0.712
2012 Sun TW, Ren WW, Xiao Q, Tang YF, Zhang YD, Li Y, Meng FK, Liu YF, Zhao MZ, Xu LM, Chen JH, Yang Z. Diastereoselective total synthesis of (±)-schindilactone A, Part 1: Construction of the ABC and FGH ring systems and initial attempts to construct the CDEF ring system. Chemistry, An Asian Journal. 7: 2321-33. PMID 22761005 DOI: 10.1002/Asia.201200363  0.7
2011 Xiao Q, Ren WW, Chen ZX, Sun TW, Li Y, Ye QD, Gong JX, Meng FK, You L, Liu YF, Zhao MZ, Xu LM, Shan ZH, Shi Y, Tang YF, et al. Diastereoselective total synthesis of (±)-schindilactone A. Angewandte Chemie (International Ed. in English). 50: 7373-7. PMID 21739547 DOI: 10.1002/Anie.201103088  0.499
2011 Xiao Q, Ren W, Chen Z, Sun T, Li Y, Ye Q, Gong J, Meng F, You L, Liu Y, Zhao M, Xu L, Shan Z, Shi Y, Tang Y, et al. Cover Picture: Diastereoselective Total Synthesis of (±)-Schindilactone A (Angew. Chem. Int. Ed. 32/2011) Angewandte Chemie International Edition. 50: 7195-7195. DOI: 10.1002/Anie.201104437  0.439
2011 Xiao Q, Ren W, Chen Z, Sun T, Li Y, Ye Q, Gong J, Meng F, You L, Liu Y, Zhao M, Xu L, Shan Z, Shi Y, Tang Y, et al. Titelbild: Diastereoselective Total Synthesis of (±)-Schindilactone A (Angew. Chem. 32/2011) Angewandte Chemie. 123: 7333-7333. DOI: 10.1002/Ange.201104437  0.444
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