| Year |
Citation |
Score |
| 2022 |
Qu J, Yan Z, Wang X, Deng J, Liu F, Rong ZQ. Nickel-catalyzed cross-coupling of epoxides with aryltriflates: rapid and regioselective construction of aryl ketones. Chemical Communications (Cambridge, England). 58: 9214-9217. PMID 35894937 DOI: 10.1039/d2cc02891c |
0.438 |
|
| 2020 |
Yang LC, Wang YN, Liu R, Luo Y, Ng XQ, Yang B, Rong ZQ, Lan Y, Shao Z, Zhao Y. Stereoselective access to [5.5.0] and [4.4.1] bicyclic compounds through Pd-catalysed divergent higher-order cycloadditions. Nature Chemistry. PMID 32719481 DOI: 10.1038/s41557-020-0503-7 |
0.472 |
|
| 2019 |
Lu S, Poh SB, Rong ZQ, Zhao Y. NHC-Catalyzed Atroposelective Acylation of Phenols: Access to Enantiopure NOBIN Analogs by Desymmetrization. Organic Letters. PMID 31339326 DOI: 10.1021/acs.orglett.9b02425 |
0.539 |
|
| 2018 |
Zhao Y, Yang LC, Tan ZY, Rong ZQ, Liu R, Wang YN. Pd-Titanium Relay Catalysis Enables Switch of Alkoxide-π-Allyl to Dienolate Reactivity for Spiro-Heterocycle Synthesis. Angewandte Chemie (International Ed. in English). PMID 29744984 DOI: 10.1002/anie.201804160 |
0.466 |
|
| 2017 |
Zhao Y, Wang YN, Yang LC, Rong ZQ, Liu TL, Liu R. Pd-Catalyzed Enantioselective [6+4] Cycloaddition of Vinyl Oxetanes with Azadienes to Access Ten-Membered Heterocycles. Angewandte Chemie (International Ed. in English). PMID 29265722 DOI: 10.1002/anie.201711648 |
0.514 |
|
| 2017 |
Rong ZQ, Lim HN, Dong G. Intramolecular Acetyl Transfer to Olefins via Catalytic C-C Bond Activation of Unstrained Ketones. Angewandte Chemie (International Ed. in English). PMID 29171904 DOI: 10.1002/Anie.201711394 |
0.483 |
|
| 2017 |
Rong ZQ, Yang LC, Liu S, Yu Z, Wang YN, Tan ZY, Huang RZ, Lan Y, Zhao Y. Nine-Membered Benzofuran-Fused Heterocycles: Enantioselective Synthesis by Pd-Catalysis and Rearrangement via Transannular Bond Formation. Journal of the American Chemical Society. PMID 29039659 DOI: 10.1021/jacs.7b09161 |
0.492 |
|
| 2017 |
Yang LC, Rong ZQ, Wang YN, Tan ZY, Wang M, Zhao Y. Construction of Nine-Membered Heterocycles through Palladium-Catalyzed Formal [5+4] Cycloaddition. Angewandte Chemie (International Ed. in English). PMID 28165185 DOI: 10.1002/anie.201611474 |
0.543 |
|
| 2016 |
Zhao Y, Rong ZQ, Wang M, Chow CH. Catalyst-Enabled Diastereodivergent aza-Diels-Alder Reaction: Complementarity of N-Heterocyclic Carbene and Chiral Amine. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27219298 DOI: 10.1002/chem.201601626 |
0.529 |
|
| 2015 |
Rong ZQ, Zhang Y, Chua RH, Pan HJ, Zhao Y. Dynamic Kinetic Asymmetric Amination of Alcohols: From A Mixture of Four Isomers to Diastereo- and Enantiopure α-Branched Amines. Journal of the American Chemical Society. 137: 4944-7. PMID 25837014 DOI: 10.1021/jacs.5b02212 |
0.321 |
|
| 2014 |
Wang M, Rong ZQ, Zhao Y. Stereoselective synthesis of ε-lactones or spiro-heterocycles through NHC-catalyzed annulation: divergent reactivity by catalyst control. Chemical Communications (Cambridge, England). 50: 15309-12. PMID 25352217 DOI: 10.1039/c4cc07788a |
0.492 |
|
| 2013 |
Rong ZQ, Pan HJ, Yan HL, Zhao Y. Enantioselective oxidation of 1,2-diols with quinine-derived urea organocatalyst. Organic Letters. 16: 208-11. PMID 24320008 DOI: 10.1021/ol4032045 |
0.418 |
|
| 2011 |
Rong ZQ, Jia MQ, You SL. Enantioselective N-heterocyclic carbene-catalyzed Michael addition to α,β-unsaturated aldehydes by redox oxidation. Organic Letters. 13: 4080-3. PMID 21732659 DOI: 10.1021/Ol201595F |
0.518 |
|
| 2011 |
Wu QF, Liu WB, Zhuo CX, Rong ZQ, Ye KY, You SL. Iridium-catalyzed intramolecular asymmetric allylic dearomatization of phenols. Angewandte Chemie (International Ed. in English). 50: 4455-8. PMID 21472834 DOI: 10.1002/Anie.201100206 |
0.452 |
|
| 2011 |
Jia MQ, Li Y, Rong ZQ, You SL. Synthesis of (1R,2R)-DPEN-derived triazolium salts and their application in asymmetric intramolecular Stetter reactions. Organic & Biomolecular Chemistry. 9: 2072-4. PMID 21340086 DOI: 10.1039/C1Ob00025J |
0.555 |
|
| 2010 |
Gu Q, Rong ZQ, Zheng C, You SL. Desymmetrization of cyclohexadienones via Brønsted acid-catalyzed enantioselective oxo-Michael reaction. Journal of the American Chemical Society. 132: 4056-7. PMID 20205477 DOI: 10.1021/Ja100207S |
0.617 |
|
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