Year |
Citation |
Score |
2023 |
Li Q, Liu Y, Li C. Picolinaldehyde-Zinc(II)-Palladium(0) Catalytic System for the Asymmetric α-Allylation of N-unprotected Amino Esters. Chemistry (Weinheim An Der Bergstrasse, Germany). e202301348. PMID 37237423 DOI: 10.1002/chem.202301348 |
0.379 |
|
2022 |
Liu F, Ding C, Tian S, Lu SM, Feng C, Tu D, Liu Y, Wang W, Li C. Electrocatalytic NAD reduction hydrogen atom-coupled electron transfer. Chemical Science. 13: 13361-13367. PMID 36507184 DOI: 10.1039/d2sc02691k |
0.333 |
|
2021 |
Wang QN, Liu X, Wang K, Liu Y, Lu SM, Li C. Direct synthesis of -methyl benzaldehyde from acetaldehyde via an organic amine-catalyzed dehydrogenation mechanism. Iscience. 24: 103028. PMID 34522868 DOI: 10.1016/j.isci.2021.103028 |
0.423 |
|
2021 |
Lin X, Liu X, Wang K, Li Q, Liu Y, Li C. Biomimetic approach to the catalytic enantioselective synthesis of tetracyclic isochroman. Nature Communications. 12: 4958. PMID 34400633 DOI: 10.1038/s41467-021-25198-y |
0.434 |
|
2020 |
Li C, Liu X, Wang K, Liu Y. Divergent Asymmetric Reactions of ortho-Quinone Methides with α-Thiocyanato Indanones for the Synthesis of Spiro- and Fused-indanones. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 32909264 DOI: 10.1002/chem.202003647 |
0.441 |
|
2020 |
Lin X, Liu Y, Li C. Allylsilane Reagent-controlled Divergent Asymmetric Catalytic Reactions of 2-Naphthoquinone-1-Methide. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 32815199 DOI: 10.1002/chem.202002814 |
0.399 |
|
2019 |
Chen P, Wang K, Zhang B, Guo W, Liu Y, Li C. Water enables an asymmetric cross reaction of α-keto acids with α-keto esters for the synthesis of quaternary isotetronic acids. Chemical Communications (Cambridge, England). PMID 31595272 DOI: 10.1039/C9Cc06356K |
0.411 |
|
2019 |
Liu X, Wang K, Guo W, Liu Y, Li C. Correction: An organic-base catalyzed asymmetric 1,4-addition of tritylthiol to in situ generated aza-o-quinone methides at the HO/DCM interface. Chemical Communications (Cambridge, England). PMID 31355375 DOI: 10.1039/c9cc90341k |
0.338 |
|
2019 |
Liu X, Wang K, Guo W, Liu Y, Li C. An organic-base catalyzed asymmetric 1,4-addition of tritylthiol to in situ generated aza-o-quinone methides at the HO/DCM interface. Chemical Communications (Cambridge, England). PMID 30746537 DOI: 10.1039/C8Cc09382B |
0.387 |
|
2017 |
Chen P, Wang K, Guo W, Liu X, Liu Y, Li C. Enantioselective Reactions of 2-Sulfonylalkyl Phenols with Allenic Esters: Dynamic Kinetic Resolution and [4+2] Cycloaddition Involving ortho-Quinone Methide Intermediates. Angewandte Chemie (International Ed. in English). PMID 28240410 DOI: 10.1002/Anie.201700250 |
0.44 |
|
2017 |
Guo W, Liu Y, Li C. Asymmetric Catalytic 1,2-Hydroperoxidation of Isatin-Derived Ketimine with Hydrogen Peroxide in the Crowding Environment of PEGs. Organic Letters. PMID 28230371 DOI: 10.1021/acs.orglett.7b00032 |
0.43 |
|
2016 |
Cheng P, Guo W, Chen P, Liu Y, Du X, Li C. The enantioselective construction of chiral spirooxindole-based 4-thiazolidinone via asymmetric catalytic formal [3+2] annulation using a bifunctional catalyst. Chemical Communications (Cambridge, England). PMID 26831820 DOI: 10.1039/c5cc10292h |
0.415 |
|
2015 |
Wu Y, Yuan B, Li M, Zhang WH, Liu Y, Li C. Well-defined BiOCl colloidal ultrathin nanosheets: synthesis, characterization, and application in photocatalytic aerobic oxidation of secondary amines. Chemical Science. 6: 1873-1878. PMID 29308137 DOI: 10.1039/c4sc03229b |
0.379 |
|
2015 |
Chen P, Lu SM, Guo W, Liu Y, Li C. A highly enantioselective thiolation of sulfonyl indoles to access 3-sec-sulfur-substituted indoles in water. Chemical Communications (Cambridge, England). PMID 26497910 DOI: 10.1039/c5cc07721d |
0.424 |
|
2015 |
Guo W, Wu B, Zhou X, Chen P, Wang X, Zhou YG, Liu Y, Li C. Formal asymmetric catalytic thiolation with a bifunctional catalyst at a water-oil interface: synthesis of benzyl thiols. Angewandte Chemie (International Ed. in English). 54: 4522-6. PMID 25694264 DOI: 10.1002/Anie.201409894 |
0.429 |
|
2014 |
Yuan B, Chong R, Zhang B, Li J, Liu Y, Li C. Photocatalytic aerobic oxidation of amines to imines on BiVO4 under visible light irradiation. Chemical Communications (Cambridge, England). 50: 15593-6. PMID 25360458 DOI: 10.1039/c4cc07097f |
0.316 |
|
2014 |
Guo W, Wang X, Zhang B, Shen S, Zhou X, Wang P, Liu Y, Li C. Facile synthesis of chiral spirooxindole-based isotetronic acids and 5-1H-pyrrol-2-ones through cascade reactions with bifunctional organocatalysts. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 8545-50. PMID 24895171 DOI: 10.1002/chem.201402945 |
0.441 |
|
2012 |
Zhang B, Jiang Z, Zhou X, Lu S, Li J, Liu Y, Li C. The synthesis of chiral isotetronic acids with amphiphilic imidazole/pyrrolidine catalysts assembled in oil-in-water emulsion droplets. Angewandte Chemie (International Ed. in English). 51: 13159-62. PMID 23161532 DOI: 10.1002/anie.201206438 |
0.417 |
|
2012 |
Wang C, Jia G, Zhou J, Li Y, Liu Y, Lu S, Li C. Enantioselective Diels-Alder reactions with G-quadruplex DNA-based catalysts. Angewandte Chemie (International Ed. in English). 51: 9352-5. PMID 22893515 DOI: 10.1002/anie.201204850 |
0.378 |
|
2012 |
Wang C, Li Y, Jia G, Liu Y, Lu S, Li C. Enantioselective Friedel-Crafts reactions in water catalyzed by a human telomeric G-quadruplex DNA metalloenzyme. Chemical Communications (Cambridge, England). 48: 6232-4. PMID 22595813 DOI: 10.1039/c2cc31320k |
0.379 |
|
Show low-probability matches. |