Year |
Citation |
Score |
2024 |
Wu Q, Zhang Z, Chong Q, Meng F. Photoredox/Cobalt-Catalyzed Chemo-, Regio-, Diastereo- and Enantioselective Reductive Coupling of 1,1-Disubstituted Allenes and Cyclobutenes. Angewandte Chemie (International Ed. in English). e202416524. PMID 39715712 DOI: 10.1002/anie.202416524 |
0.499 |
|
2024 |
Lin C, Wu Q, Wang Y, Chong Q, Meng F. Recent advances in catalytic enantioselective carbometallation of cyclopropenes and cyclobutenes. Chemical Communications (Cambridge, England). PMID 39380324 DOI: 10.1039/d4cc04192e |
0.432 |
|
2024 |
Wang Y, Wang D, Wang S, Chong Q, Zhang Z, Meng F. Cobalt-Catalyzed Regio-, Diastereo- and Enantioselective Reductive Coupling of 1,3-Dienes and Aldehydes. Angewandte Chemie (International Ed. in English). e202413313. PMID 39230052 DOI: 10.1002/anie.202413313 |
0.506 |
|
2024 |
Wang H, Jie X, Su T, Wu Q, Kuang J, Sun Z, Zhao Y, Chong Q, Guo Y, Zhang Z, Meng F. Cobalt-Catalyzed Chemo- and Stereoselective Transfer Semihydrogenation of 1,3-Dienes with Water as a Hydrogen Source. Journal of the American Chemical Society. PMID 39110419 DOI: 10.1021/jacs.4c06925 |
0.438 |
|
2024 |
Lin C, Zhang J, Sun Z, Guo Y, Chong Q, Zhang Z, Meng F. Cobalt-Catalyzed Enantioselective Alkenylation of Aldehydes. Angewandte Chemie (International Ed. in English). e202405290. PMID 38818654 DOI: 10.1002/anie.202405290 |
0.487 |
|
2024 |
Wang H, Jie X, Chong Q, Meng F. Pathway-divergent coupling of 1,3-enynes with acrylates through cascade cobalt catalysis. Nature Communications. 15: 3427. PMID 38654019 DOI: 10.1038/s41467-024-47719-1 |
0.465 |
|
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 |
0.444 |
|
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 |
0.439 |
|
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 |
0.535 |
|
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 |
0.331 |
|
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 |
0.413 |
|
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 |
0.428 |
|
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 |
0.514 |
|
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 |
0.54 |
|
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 |
0.535 |
|
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 |
0.58 |
|
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 |
0.615 |
|
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 |
0.529 |
|
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 |
0.534 |
|
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 |
0.578 |
|
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 |
0.728 |
|
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 |
0.7 |
|
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 |
0.71 |
|
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 |
0.616 |
|
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 |
0.709 |
|
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 |
0.697 |
|
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 |
0.495 |
|
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 |
0.435 |
|
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 |
0.44 |
|
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