Year |
Citation |
Score |
2023 |
Kong D, Zhang M, Zhang Y, Yu Z, Cao H, Wu J. Photocatalyzed regioselective hydrosilylation for the divergent synthesis of geminal and vicinal borosilanes. Nature Communications. 14: 2525. PMID 37130840 DOI: 10.1038/s41467-023-38224-y |
0.408 |
|
2023 |
Fan X, Zhang M, Gao Y, Zhou Q, Zhang Y, Yu J, Xu W, Yan J, Liu H, Lei Z, Ter YC, Chanmungkalakul S, Lum Y, Liu X, Cui G, et al. Stepwise on-demand functionalization of multihydrosilanes enabled by a hydrogen-atom-transfer photocatalyst based on eosin Y. Nature Chemistry. PMID 36894703 DOI: 10.1038/s41557-023-01155-8 |
0.383 |
|
2023 |
Tang H, Zhang M, Zhang Y, Luo P, Ravelli D, Wu J. Direct Synthesis of Thioesters from Feedstock Chemicals and Elemental Sulfur. Journal of the American Chemical Society. 145: 5846-5854. PMID 36854068 DOI: 10.1021/jacs.2c13157 |
0.424 |
|
2023 |
Yuan Y, Zhang M, Tang X, Piper JL, Peng ZH, Ma JA, Wu J, Zhang FG. Photoinduced Defluorinative Branch-Selective Olefination of Multifluoro (Hetero)arenes. Organic Letters. PMID 36728281 DOI: 10.1021/acs.orglett.3c00115 |
0.339 |
|
2022 |
Zhang M, Zhang J, Li Q, Shi Y. Iron-mediated ligand-to-metal charge transfer enables 1,2-diazidation of alkenes. Nature Communications. 13: 7880. PMID 36564406 DOI: 10.1038/s41467-022-35344-9 |
0.31 |
|
2022 |
Li Q, Dai P, Tang H, Zhang M, Wu J. Photomediated reductive coupling of nitroarenes with aldehydes for amide synthesis. Chemical Science. 13: 9361-9365. PMID 36093005 DOI: 10.1039/d2sc03047k |
0.492 |
|
2021 |
Yan J, Tang H, Kuek EJR, Shi X, Liu C, Zhang M, Piper JL, Duan S, Wu J. Divergent functionalization of aldehydes photocatalyzed by neutral eosin Y with sulfone reagents. Nature Communications. 12: 7214. PMID 34893628 DOI: 10.1038/s41467-021-27550-8 |
0.424 |
|
2020 |
Zhang J, Zhang M. Retraction of "Harnessing Thiol as a Benzyl Reagent for Photocatalytic Reductive Benzylation of Imines". Organic Letters. 22: 2112. PMID 31984751 DOI: 10.1021/acs.orglett.0c00065 |
0.303 |
|
2018 |
Zhang M, Xie J, Zhu C. A general deoxygenation approach for synthesis of ketones from aromatic carboxylic acids and alkenes. Nature Communications. 9: 3517. PMID 30158628 DOI: 10.1038/s41467-018-06019-1 |
0.431 |
|
2017 |
Ruzi R, Zhang M, Ablajan K, Zhu C. Photoredox-Catalyzed Deoxygenative Intramolecular Acylation of Biarylcarboxylic Acids: Access to Fluorenones. The Journal of Organic Chemistry. PMID 28949539 DOI: 10.1021/Acs.Joc.7B02197 |
0.475 |
|
2017 |
Zhang M, Li N, Tao X, Ruzi R, Yu S, Zhu C. Selective reduction of carboxylic acids to aldehydes with hydrosilane via photoredox catalysis. Chemical Communications (Cambridge, England). PMID 28861564 DOI: 10.1039/C7Cc05570F |
0.385 |
|
2017 |
Zhang M, Xi J, Ruzi R, Li N, Wu Z, Li W, Zhu C. Domino-fluorination-protodefluorination enables decarboxylative cross-coupling of α-oxocarboxylic acids with styrene via photoredox catalysis. The Journal of Organic Chemistry. PMID 28809563 DOI: 10.1021/acs.joc.7b01054 |
0.323 |
|
2017 |
Zhang M, Ruzi R, Xi J, Li N, Wu Z, Li W, Yu S, Zhu C. Photoredox-Catalyzed Hydroacylation of Olefins Employing Carboxylic Acids and Hydrosilanes. Organic Letters. PMID 28612606 DOI: 10.1021/Acs.Orglett.7B01391 |
0.356 |
|
2017 |
Wu Z, Xu P, Zhou N, Duan Y, Zhang M, Zhu C. [3+2] Cycloaddition of azide with aldehyde hydrazone through an aminyl radical-polar crossover strategy. Chemical Communications (Cambridge, England). PMID 28044151 DOI: 10.1039/c6cc08779e |
0.32 |
|
2016 |
Zhang M, Li W, Duan Y, Xu P, Zhang S, Zhu C. Cascade Photoredox/Iodide Catalysis: Access to Difluoro-γ-lactams via Aminodifluoroalkylation of Alkenes. Organic Letters. PMID 27337532 DOI: 10.1021/acs.orglett.6b01515 |
0.408 |
|
2016 |
Li W, Duan Y, Zhang M, Cheng J, Zhu C. A photoredox catalyzed radical-radical coupling reaction: facile access to multi-substituted nitrogen heterocycles. Chemical Communications (Cambridge, England). PMID 27226386 DOI: 10.1039/c6cc02027e |
0.466 |
|
2016 |
Zhang M, Duan Y, Li W, Cheng Y, Zhu C. Visible-light-induced aerobic dearomative reaction of indole derivatives: access to heterocycle fused or spirocyclo indolones. Chemical Communications (Cambridge, England). PMID 26974291 DOI: 10.1039/c6cc00818f |
0.325 |
|
Show low-probability matches. |