Year |
Citation |
Score |
2023 |
Lai M, Zhang Y, Zhao L, Huang YH, Zhang L, Fu W, Chen P, Wang XD, Zhu T, Yang Z. Direct Arylation of Silicon Nanocrystals with Hexadehydro-Diels-Alder-Derived Benzynes. Angewandte Chemie (International Ed. in English). e202304056. PMID 37186058 DOI: 10.1002/anie.202304056 |
0.307 |
|
2022 |
Zhou P, Li W, Lan J, Zhu T. Electroredox carbene organocatalysis with iodide as promoter. Nature Communications. 13: 3827. PMID 35780238 DOI: 10.1038/s41467-022-31453-7 |
0.348 |
|
2022 |
Liu W, Hao L, Zhang J, Zhu T. Progress in the Electrochemical Reactions of Sulfonyl Compounds. Chemsuschem. e202102557. PMID 35174969 DOI: 10.1002/cssc.202102557 |
0.524 |
|
2021 |
Wang FX, Yan JL, Liu Z, Zhu T, Liu Y, Ren SC, Lv WX, Jin Z, Chi YR. Assembly of multicyclic isoquinoline scaffolds from pyridines: formal total synthesis of fredericamycin A. Chemical Science. 12: 10259-10265. PMID 34377413 DOI: 10.1039/d1sc02442f |
0.599 |
|
2020 |
Zhu T, Xu K, Wang Z. N-Heterocyclic Carbene-Organocatalyzed Arene Formation: Application in Atroposelective Synthesis of Polysubstituted Benzenes Synlett. 31: 925-932. DOI: 10.1055/S-0039-1690814 |
0.491 |
|
2019 |
Xu K, Li W, Zhu S, Zhu T. Atroposelective arene formation via carbene-catalyzed formal [4+2] cycloaddition. Angewandte Chemie (International Ed. in English). PMID 31553516 DOI: 10.1002/Anie.201910049 |
0.62 |
|
2019 |
Liu Y, Shen Y, Zhang W, Weng J, Zhao M, Zhu T, Chi YR, Yang Y, Zhang H, Huo F. Engineering channels of metal-organic frameworks to enhance catalytic selectivity. Chemical Communications (Cambridge, England). PMID 31513185 DOI: 10.1039/C9Cc06061H |
0.548 |
|
2019 |
Zhu T, Liu Y, Smetankova M, Zhuo S, Mou C, Chai H, Jin Z, Chi YR. Carbene-Catalyzed Desymmetrization and Direct Construction of Arenes with All-Carbon Quaternary Chiral Center. Angewandte Chemie (International Ed. in English). PMID 31464052 DOI: 10.1002/Anie.201910183 |
0.718 |
|
2018 |
Chen Q, Zhu T, Majhi PK, Mou C, Chai H, Zhang J, Zhuo S, Chi YR. Carbene-catalyzed enantioselective oxidative coupling of enals and di(hetero)arylmethanes. Chemical Science. 9: 8711-8715. PMID 30595836 DOI: 10.1039/C8Sc03480J |
0.617 |
|
2018 |
Zhuo S, Zhu T, Zhou L, Mou C, Chai H, Lu Y, Pan L, Jin Z, Chi YR. Access to All-Carbon Spirocycles through a Carbene and Thiourea Cocatalytic Desymmetrization Cascade Reaction. Angewandte Chemie (International Ed. in English). PMID 30476348 DOI: 10.1002/Anie.201810638 |
0.738 |
|
2017 |
Huang X, Zhu T, Huang Z, Zhang Y, Jin Z, Zanoni G, Chi YR. Carbene-Catalyzed Formal [5 + 5] Reaction for Coumarin Construction and Total Synthesis of Defucogilvocarcins. Organic Letters. PMID 29111757 DOI: 10.1021/Acs.Orglett.7B03102 |
0.679 |
|
2017 |
Chen X, Song R, Liu Y, Ooi CY, Jin Z, Zhu T, Wang H, Hao L, Chi YR. Carbene and Acid Cooperative Catalytic Reactions of Aldehydes and o-Hydroxybenzhydryl Amines for Highly Enantioselective Access to Dihydrocoumarins. Organic Letters. PMID 29068212 DOI: 10.1021/Acs.Orglett.7B02883 |
0.721 |
|
2016 |
Mou C, Zhu T, Zheng P, Yang S, Song B, Chi YR. ChemInform Abstract: Green and Rapid Access to Benzocoumarins via Direct Benzene Construction Through Base-Mediated Formal [4 + 2] Reaction and Air Oxidation. Cheminform. 47. DOI: 10.1002/CHIN.201628169 |
0.328 |
|
2016 |
Mou C, Zhu T, Zheng P, Yang S, Song BA, Chi YR. Green and Rapid Access to Benzocoumarins via Direct Benzene Construction through Base-Mediated Formal [4+2] Reaction and Air Oxidation Advanced Synthesis and Catalysis. DOI: 10.1002/Adsc.201500771 |
0.621 |
|
2015 |
Zhu T, Mou C, Li B, Smetankova M, Song BA, Chi YR. N-Heterocyclic Carbene-Catalyzed δ-Carbon LUMO Activation of Unsaturated Aldehydes. Journal of the American Chemical Society. 137: 5658-61. PMID 25910417 DOI: 10.1021/jacs.5b02219 |
0.663 |
|
2015 |
Su L, Zhu T, Xu M. ChemInform Abstract: Indium-Mediated Asymmetric Intramolecular Allenylation of N-tert-Butanesulfinyl Imines: Efficient and Practical Access to Chiral 3-Allenyl-4-aminochromanes. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201508213 |
0.337 |
|
2014 |
Zhu T, Zheng P, Mou C, Yang S, Song BA, Chi YR. Benzene construction via organocatalytic formal [3+3] cycloaddition reaction. Nature Communications. 5: 5027. PMID 25255058 DOI: 10.1038/Ncomms6027 |
0.666 |
|
2014 |
Su L, Zhu T, Xu M. Indium-mediated asymmetric intramolecular allenylation of N-tert-butanesulfinyl imines: efficient and practical access to chiral 3-allenyl-4-aminochromanes. Organic Letters. 16: 4118-4121. PMID 25068528 DOI: 10.1021/Ol501815E |
0.48 |
|
2014 |
Xu J, Mou C, Zhu T, Song BA, Chi YR. N-Heterocyclic carbene-catalyzed chemoselective cross-aza-benzoin reaction of enals with isatin-derived ketimines: access to chiral quaternary aminooxindoles. Organic Letters. 16: 3272-5. PMID 24877668 DOI: 10.1021/Ol501286E |
0.698 |
|
2014 |
Namitharan K, Zhu T, Cheng J, Zheng P, Li X, Yang S, Song BA, Chi YR. Metal and carbene organocatalytic relay activation of alkynes for stereoselective reactions. Nature Communications. 5: 3982. PMID 24865392 DOI: 10.1038/ncomms4982 |
0.605 |
|
2014 |
Fu Z, Jiang K, Zhu T, Torres J, Chi YR. Access to oxoquinoline heterocycles by N-heterocyclic carbene catalyzed ester activation for selective reaction with an enone. Angewandte Chemie (International Ed. in English). 53: 6506-10. PMID 24839111 DOI: 10.1002/Anie.201402620 |
0.705 |
|
2013 |
Fu Z, Xu J, Zhu T, Leong WW, Chi YR. β-Carbon activation of saturated carboxylic esters through N-heterocyclic carbene organocatalysis. Nature Chemistry. 5: 835-9. PMID 24056339 DOI: 10.1038/Nchem.1710 |
0.637 |
|
2013 |
Zhu T, Xu M. Chiral Sulfinamide-Olefin Ligands: Switchable Selectivity in Rhodium-Catalyzed Asymmetric 1,2-Addition of Arylboronic Acids to Aliphaticα-Ketoesters Chinese Journal of Chemistry. 31: 321-328. DOI: 10.1002/Cjoc.201300063 |
0.505 |
|
2013 |
Zhu T, Xu M. ChemInform Abstract: Chiral Sulfinamide-Olefin Ligands: Switchable Selectivity in Rhodium-Catalyzed Asymmetric 1,2-Addition of Arylboronic Acids to Aliphatic α-Ketoesters. Cheminform. 44: no-no. DOI: 10.1002/CHIN.201344091 |
0.384 |
|
2013 |
Wang H, Zhu T, Xu M. ChemInform Abstract: Rhodium-Catalyzed Enantioselective 1,2-Addition of Arylboronic Acids to Heteroaryl α-Ketoesters for Synthesis of Heteroaromatic α-Hydroxy Esters. Cheminform. 44: no-no. DOI: 10.1002/CHIN.201319115 |
0.346 |
|
2012 |
Zhu TS, Chen JP, Xu MH. Rhodium-catalyzed enantioselective addition to unsymmetrical α-diketones: tandem one-pot synthesis of optically active 3-tetrasubstituted isochroman derivatives. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 865-9. PMID 23239222 DOI: 10.1002/chem.201203701 |
0.458 |
|
2012 |
Wang H, Zhu T, Xu M. Rhodium-catalyzed enantioselective 1,2-addition of arylboronic acids to heteroaryl α-ketoesters for synthesis of heteroaromatic α-hydroxy esters. Organic and Biomolecular Chemistry. 10: 9158-9164. PMID 23011218 DOI: 10.1039/C2Ob26316E |
0.526 |
|
2012 |
Zhu T, Xu M. Efficient synthesis of optically active α-quaternary amino acids by highly diastereoselective [2,3]-rearrangement of allylic ammonium ylides. Chemical Communications. 48: 7274-7276. PMID 22705632 DOI: 10.1039/C2Cc33027J |
0.427 |
|
2012 |
Jin S, Wang H, Zhu T, Xu M. Design of N-cinnamyl sulfinamides as new sulfur-containing olefin ligands for asymmetric catalysis: achieving structural simplicity with a categorical linear framework. Organic and Biomolecular Chemistry. 10: 1764-1768. PMID 22234574 DOI: 10.1039/C2Ob06723D |
0.502 |
|
2012 |
Zhu T, Jin S, Xu M. Rhodium‐Catalyzed, Highly Enantioselective 1,2‐Addition of Aryl Boronic Acids to α‐Ketoesters and α‐Diketones Using Simple, Chiral Sulfur–Olefin Ligands Angewandte Chemie. 51: 780-783. PMID 22134900 DOI: 10.1002/Anie.201106972 |
0.447 |
|
2012 |
Zhu T, Xu M. ChemInform Abstract: Efficient Synthesis of Optically Active α-Quaternary Amino Acids by Highly Diastereoselective [2,3]-Rearrangement of Allylic Ammonium Ylides. Cheminform. 43: no-no. DOI: 10.1002/CHIN.201245208 |
0.319 |
|
2012 |
Zhu T, Jin S, Xu M. ChemInform Abstract: Rhodium-Catalyzed, Highly Enantioselective 1,2-Addition of Aryl Boronic Acids to α-Ketoesters and α-Diketones Using Simple, Chiral Sulfur-Olefin Ligands. Cheminform. 43: no-no. DOI: 10.1002/CHIN.201223023 |
0.386 |
|
2011 |
Qi W, Zhu T, Xu M. Design of chiral sulfoxide-olefins as a new class of sulfur-based olefin ligands for asymmetric catalysis. Organic Letters. 13: 3410-3413. PMID 21634419 DOI: 10.1021/Ol201151R |
0.542 |
|
2011 |
Qi W, Zhu T, Xu M. ChemInform Abstract: Design of Chiral Sulfoxide-Olefins as a New Class of Sulfur-Based Olefin Ligands for Asymmetric Catalysis. Cheminform. 42: no-no. DOI: 10.1002/CHIN.201145075 |
0.306 |
|
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