| Year |
Citation |
Score |
| 2023 |
Shao H, Adebomi V, Bruce A, Raj M, Houk KN. Intramolecular Hydrogen Bonding Enables a Zwitterionic Mechanism for Macrocyclic Peptide Formation: Computational Mechanistic Studies of CyClick Chemistry. Angewandte Chemie (International Ed. in English). e202307210. PMID 37475575 DOI: 10.1002/anie.202307210 |
0.365 |
|
| 2023 |
Hejna BG, Ganley JM, Shao H, Tian H, Ellefsen JD, Fastuca NJ, Houk KN, Miller SJ, Knowles RR. Catalytic Asymmetric Hydrogen Atom Transfer: Enantioselective Hydroamination of Alkenes. Journal of the American Chemical Society. PMID 37432783 DOI: 10.1021/jacs.3c04591 |
0.459 |
|
| 2023 |
Kleinmans R, Dutta S, Ozols K, Shao H, Schäfer F, Thielemann RE, Chan HT, Daniliuc CG, Houk KN, Glorius F. -Selective Dearomative [2π + 2σ] Photocycloadditions of Bicyclic Aza-Arenes. Journal of the American Chemical Society. PMID 37232562 DOI: 10.1021/jacs.3c02961 |
0.484 |
|
| 2021 |
Shao H, Chakrabarty S, Qi X, Takacs JM, Liu P. Ligand Conformational Flexibility Enables Enantioselective Tertiary C-B Bond Formation in the Phosphonate-Directed Catalytic Asymmetric Alkene Hydroboration. Journal of the American Chemical Society. PMID 33750118 DOI: 10.1021/jacs.1c01303 |
0.627 |
|
| 2020 |
Gao DW, Gao Y, Shao H, Qiao TZ, Wang X, Sanchez BB, Chen JS, Liu P, Engle KM. Cascade CuH-Catalysed Conversion of Alkynes to Enantioenriched 1,1-Disubstituted Products. Nature Catalysis. 3: 23-29. PMID 32420528 DOI: 10.1038/s41929-019-0384-6 |
0.415 |
|
| 2020 |
Shao H, Wang Y, Bielawski CW, Liu P. Computational Investigations of the Effects of N-Heterocyclic Carbene Ligands on the Mechanism, Reactivity, and Regioselectivity of Rh-Catalyzed Hydroborations Acs Catalysis. 10: 3820-3827. DOI: 10.1021/Acscatal.0C00111 |
0.443 |
|
| 2019 |
Medina JM, Kang T, Erbay TG, Shao H, Gallego GM, Yang S, Tran-Dubé M, Richardson PF, Derosa J, Helsel RT, Patman RL, Wang F, Ashcroft CP, Braganza JF, McAlpine I, et al. Cu-Catalyzed Hydroboration of Benzylidenecyclopropanes: Reaction Optimization, (Hetero)Aryl Scope, and Origins of Pathway Selectivity. Acs Catalysis. 9: 11130-11136. PMID 32617185 DOI: 10.1021/Acscatal.9B03557 |
0.623 |
|
| 2019 |
Ryu Y, Shao H, Ahumada G, Liu P, Bielawski CW. Redox-switchable olefin cross metathesis (CM) reactions and acyclic diene metathesis (ADMET) polymerizations Materials Chemistry Frontiers. 3: 2083-2089. DOI: 10.1039/C9Qm00391F |
0.452 |
|
| 2019 |
Medina JM, Kang T, Erbay TG, Shao H, Gallego GM, Yang S, Tran-Dubé M, Richardson PF, Derosa J, Helsel RT, Patman RL, Wang F, Ashcroft CP, Braganza JF, McAlpine I, et al. Cu-Catalyzed Hydroboration of Benzylidenecyclopropanes: Reaction Optimization, (Hetero)Aryl Scope, and Origins of Pathway Selectivity Acs Catalysis. 9: 11130-11136. DOI: 10.1021/acscatal.9b03557 |
0.631 |
|
| 2018 |
Chu CK, Lin TP, Shao H, Liberman-Martin AL, Liu P, Grubbs RH. Disentangling Ligand Effects on Metathesis Catalyst Activity: Experimental and Computational Studies of Ruthenium-Aminophosphine Complexes. Journal of the American Chemical Society. PMID 29621881 DOI: 10.1021/Jacs.8B02324 |
0.513 |
|
| 2017 |
Grandner JM, Shao H, Grubbs RH, Liu P, Houk KN. The Origins of the Stereoretentive Mechanism of Olefin Metathesis with Ru-Dithiolate Catalysts. The Journal of Organic Chemistry. PMID 28841319 DOI: 10.1021/Acs.Joc.7B02129 |
0.54 |
|
| 2017 |
Lastovickova DN, Teator AJ, Shao H, Liu P, Bielawski CW. A redox-switchable ring-closing metathesis catalyst Inorganic Chemistry Frontiers. 4: 1525-1532. DOI: 10.1039/C7Qi00018A |
0.45 |
|
| 2017 |
Teator AJ, Shao H, Lu G, Liu P, Bielawski CW. A Photoswitchable Olefin Metathesis Catalyst Organometallics. 36: 490-497. DOI: 10.1021/Acs.Organomet.6B00913 |
0.591 |
|
| 2016 |
Lastovickova D, Shao H, Lu G, Liu P, Bielawski CW. A Ring-Opening Metathesis Polymerization Catalyst That Exhibits Redox-Switchable Monomer Selectivities. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27977049 DOI: 10.1002/Chem.201605738 |
0.556 |
|
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