| Year |
Citation |
Score |
| 2020 |
Schuster CH, Dropinski JF, Shevlin M, Li H, Chen S. Ruthenium-Catalyzed Enantioselective Hydrogenation of Hydrazones. Organic Letters. PMID 32946691 DOI: 10.1021/acs.orglett.0c02756 |
0.477 |
|
| 2020 |
Patel NR, Nawrat CC, McLaughlin M, Xu Y, Huffman MA, Yang H, Li H, Whittaker AM, Andreani T, Lévesque F, Fryszkowska A, Brunskill A, Tschaen DM, Maloney KM. Synthesis of Islatravir Enabled by a Catalytic, Enantioselective Alkynylation of a Ketone. Organic Letters. PMID 32516536 DOI: 10.1021/Acs.Orglett.0C01431 |
0.421 |
|
| 2018 |
Wang F, Shi X, Nan F, Li H, Wang Q, Yu H, Huang Q, Yang W. The investigation of terpolymerization of ethylene/propylene/ω-cl-α-vinyl monomers catalyzed by Cat.L-Pd catalyst Scientia Sinica Chimica. 48: 609-619. DOI: 10.1360/N032017-00199 |
0.33 |
|
| 2017 |
Ji Y, Li H, Hyde AM, Chen Q, Belyk KM, Lexa KW, Yin J, Sherer EC, Williamson RT, Brunskill A, Ren S, Campeau LC, Davies IW, Ruck RT. A rational pre-catalyst design for bis-phosphine mono-oxide palladium catalyzed reactions. Chemical Science. 8: 2841-2851. PMID 28553522 DOI: 10.1039/C6Sc05472B |
0.361 |
|
| 2016 |
Li H, Wang J, He L, Nan F, Wang F, Yang W, Zhang M, Sun T, Huang Q, Yi J. Study on Hydrogen Sensitivity of Ziegler⁻Natta Catalysts with Novel Cycloalkoxy Silane Compounds as External Electron Donor. Polymers. 8. PMID 30974714 DOI: 10.3390/polym8120433 |
0.338 |
|
| 2010 |
Li H, Liu X, Wu F, Tang L, Deng L. Elucidation of the active conformation of cinchona alkaloid catalyst and chemical mechanism of alcoholysis of meso anhydrides. Proceedings of the National Academy of Sciences of the United States of America. 107: 20625-9. PMID 20566889 DOI: 10.1073/Pnas.1004439107 |
0.664 |
|
| 2009 |
Li H, Song J, Deng L. Catalytic enantioselective conjugate additions with α,β-unsaturated sulfones. Tetrahedron. 65: 3139-3148. PMID 20161246 DOI: 10.1016/J.Tet.2008.11.054 |
0.584 |
|
| 2007 |
Wang Y, Li H, Wang YQ, Liu Y, Foxman BM, Deng L. Asymmetric Diels-Alder reactions of 2-pyrones with a bifunctional organic catalyst. Journal of the American Chemical Society. 129: 6364-5. PMID 17469829 DOI: 10.1021/Ja070859H |
0.609 |
|
| 2006 |
Li H, Wang YQ, Deng L. Enantioselective Friedel-Crafts reaction of indoles with carbonyl compounds catalyzed by bifunctional cinchona alkaloids. Organic Letters. 8: 4063-5. PMID 16928074 DOI: 10.1021/ol061552a |
0.552 |
|
| 2006 |
Wang YQ, Song J, Hong R, Li H, Deng L. Asymmetric Friedel-crafts reaction of indoles with imines by an organic catalyst. Journal of the American Chemical Society. 128: 8156-7. PMID 16787078 DOI: 10.1021/Ja062700V |
0.632 |
|
| 2006 |
Li H, Wang B, Deng L. Enantioselective nitroaldol reaction of alpha-ketoesters catalyzed by cinchona alkaloids. Journal of the American Chemical Society. 128: 732-3. PMID 16417358 DOI: 10.1021/Ja057237L |
0.638 |
|
| 2006 |
Wu F, Li H, Hong R, Deng L. Construction of quaternary stereocenters by efficient and practical conjugate additions to alpha,beta-unsaturated ketones with a chiral organic catalyst. Angewandte Chemie (International Ed. in English). 45: 947-50. PMID 16385604 DOI: 10.1002/Anie.200502658 |
0.653 |
|
| 2005 |
Li H, Song J, Liu X, Deng L. Catalytic enantioselective C-C bond forming conjugate additions with vinyl sulfones. Journal of the American Chemical Society. 127: 8948-9. PMID 15969561 DOI: 10.1021/Ja0511063 |
0.569 |
|
| 2005 |
Liu X, Li H, Deng L. Highly enantioselective amination of alpha-substituted alpha-cyanoacetates with chiral catalysts accessible from both quinine and quinidine. Organic Letters. 7: 167-9. PMID 15646949 DOI: 10.1021/Ol048190W |
0.566 |
|
| 2004 |
Li H, Wang Y, Tang L, Wu F, Liu X, Guo C, Foxman BM, Deng L. Stereocontrolled creation of adjacent quaternary and tertiary stereocenters by a catalytic conjugate addition. Angewandte Chemie (International Ed. in English). 44: 105-8. PMID 15565669 DOI: 10.1002/Anie.200461923 |
0.663 |
|
| 2004 |
Li H, Wang Y, Tang L, Deng L. Highly enantioselective conjugate addition of malonate and beta-ketoester to nitroalkenes: asymmetric C-C bond formation with new bifunctional organic catalysts based on cinchona alkaloids. Journal of the American Chemical Society. 126: 9906-7. PMID 15303849 DOI: 10.1021/Ja047281L |
0.668 |
|
| 2002 |
Hang J, Li H, Deng L. Development of a rapid, room-temperature dynamic kinetic resolution for efficient asymmetric synthesis of alpha-aryl amino acids. Organic Letters. 4: 3321-4. PMID 12227779 DOI: 10.1021/Ol026660L |
0.638 |
|
| 2002 |
Hang J, Li H, Deng L. Development of a rapid, room-temperature dynamic kinetic resolution for efficient asymmetric synthesis of α-aryl amino acids Organic Letters. 4: 3321-3324. DOI: 10.1021/ol026660l |
0.562 |
|
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