| Year |
Citation |
Score |
| 2023 |
Xing L, Yang Q, Zhu C, Bai Y, Tang Y, Rueping M, Cai Y. Poly(heptazine imide) ligand exchange enables remarkable low catalyst loadings in heterogeneous metallaphotocatalysis. Nature Communications. 14: 1501. PMID 36932064 DOI: 10.1038/s41467-023-37113-8 |
0.556 |
|
| 2022 |
Li H, Yang Q, Xu L, Wei J, Tang Y, Cai Y. Cu(I)/Chiral Vanadium Complex Cooperatively Catalyzed Asymmetric Sulfonation/Rearrangement of Alkenylfurans. Organic Letters. PMID 36322889 DOI: 10.1021/acs.orglett.2c03304 |
0.439 |
|
| 2022 |
Wei J, Tang Y, Yang Q, Li H, He D, Cai Y. Asymmetric Ketoalkylation/Rearrangement of Alkyenlfurans via Synergistic Photoredox/Brønsted Acid Catalysis. Organic Letters. PMID 36269030 DOI: 10.1021/acs.orglett.2c03040 |
0.408 |
|
| 2022 |
Zou J, Xu L, Tang Y, Wang W, Cai Y. Organocatalytic Asymmetric Synthesis of Bridged Tetrahydrobenzo[]azepines/oxepines. Organic Letters. PMID 36169238 DOI: 10.1021/acs.orglett.2c02833 |
0.531 |
|
| 2021 |
Xu L, Li H, Xing L, Yang Q, Tang Y, Cai Y. -Aza-Piancatelli Rearrangement Triggered Cascade Reaction of Methyl Furylacrylates with Anilines to Access Cyclopenta[]pyrrolidinones. The Journal of Organic Chemistry. PMID 34905369 DOI: 10.1021/acs.joc.1c02546 |
0.363 |
|
| 2020 |
Xu L, Yang Q, Zhong S, Li H, Tang Y, Cai Y. Ln(III)/Chiral Brønsted Acid Catalyzed Asymmetric Cascade Ring Opening/Aza-Piancatelli Rearrangement of D-A Cyclopropanes. Organic Letters. PMID 33170722 DOI: 10.1021/acs.orglett.0c03413 |
0.495 |
|
| 2018 |
Cai Y, Liu X, Zhou P, Feng X. Asymmetric Catalytic Halofunctionalization of α,β-Unsaturated Carbonyl Compounds. The Journal of Organic Chemistry. PMID 30339377 DOI: 10.1021/Acs.Joc.8B01951 |
0.664 |
|
| 2018 |
Cai Y, Tang Y, Fan L, Lefebvre Q, Hou H, Rueping M. Heterogeneous Visible-Light Photoredox Catalysis with Graphitic Carbon Nitride for α-Aminoalkyl Radical Additions, Allylations, and Heteroarylations Acs Catalysis. 8: 9471-9476. DOI: 10.1021/Acscatal.8B02937 |
0.529 |
|
| 2017 |
Yue H, Guo L, Liao HH, Cai Y, Zhu C, Rueping M. Catalytic Ester and Amide to Amine Interconversion: Nickel-Catalyzed Decarbonylative Amination of Esters and Amides by C-O and C-C Bond Activation. Angewandte Chemie (International Ed. in English). PMID 28294473 DOI: 10.1002/Anie.201611819 |
0.604 |
|
| 2016 |
Cai Y, Tang Y, Atodiresei I, Rueping M. Catalytic Asymmetric Piancatelli Rearrangement: Brønsted Acid Catalyzed 4π Electrocyclization for the Synthesis of Multisubstituted Cyclopentenones. Angewandte Chemie (International Ed. in English). PMID 27723211 DOI: 10.1002/Anie.201608023 |
0.685 |
|
| 2016 |
Zhou P, Cai Y, Zhong X, Luo W, Kang T, Li J, Liu X, Lin L, Feng X. Catalytic Asymmetric Intra- and Intermolecular Haloetherification of Enones: An Efficient Approach to (−)-Centrolobine Acs Catalysis. 6: 7778-7783. DOI: 10.1021/Acscatal.6B02048 |
0.725 |
|
| 2015 |
Cai Y, Zhou P, Liu X, Zhao J, Lin L, Feng X. Diastereoselectively switchable asymmetric haloaminocyclization for the synthesis of cyclic sulfamates. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 6386-9. PMID 25760895 DOI: 10.1002/Chem.201500454 |
0.803 |
|
| 2015 |
Zhou P, Cai Y, Lin L, Lian X, Xia Y, Liu X, Feng X. ChemInform Abstract: Asymmetric Synthesis of Spirocyclic Oxindole-Fused Tetrahydrothiophenes via N,N′-Dioxide-Nickel(II) Catalyzed Domino Reaction of 1,4-Dithiane-2,5-diol with 3-Alkenyloxindoles. Cheminform. 46: no-no. DOI: 10.1002/chin.201530131 |
0.683 |
|
| 2015 |
Zhou P, Cai Y, Lin L, Lian X, Xia Y, Liu X, Feng X. Asymmetric synthesis of spirocyclic oxindole-fused tetrahydrothiophenes via n,n-dioxide-nickel(ii) catalyzed domino reaction of 1,4-dithiane-2,5-diol with 3-alkenyloxindoles Advanced Synthesis and Catalysis. 357: 695-700. DOI: 10.1002/Adsc.201400964 |
0.711 |
|
| 2014 |
Chen W, Lin L, Cai Y, Xia Y, Cao W, Liu X, Feng X. Catalytic asymmetric [3+2] cycloaddition of aromatic aldehydes with oxiranes by C-C bond cleavage of epoxides: highly efficient synthesis of chiral 1,3-dioxolanes. Chemical Communications (Cambridge, England). 50: 2161-3. PMID 24430105 DOI: 10.1039/C3Cc48606K |
0.7 |
|
| 2013 |
Cai Y, Liu X, Zhou P, Kuang Y, Lin L, Feng X. Iron-catalyzed asymmetric haloamination reactions. Chemical Communications (Cambridge, England). 49: 8054-6. PMID 23903004 DOI: 10.1039/C3Cc44421J |
0.698 |
|
| 2013 |
Wang Z, Zhang Z, Yao Q, Liu X, Cai Y, Lin L, Feng X. Highly stereoselective conjugate addition and α-alkynylation reaction with electron-deficient alkynes catalyzed by chiral scandium(III) complexes. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 8591-6. PMID 23670887 DOI: 10.1002/Chem.201300816 |
0.772 |
|
| 2013 |
Xie M, Liu X, Wu X, Cai Y, Lin L, Feng X. Catalytic asymmetric [8+2] cycloaddition: synthesis of cycloheptatriene-fused pyrrole derivatives. Angewandte Chemie (International Ed. in English). 52: 5604-7. PMID 23606276 DOI: 10.1002/Anie.201209601 |
0.711 |
|
| 2012 |
Xiao X, Liu X, Dong S, Cai Y, Lin L, Feng X. Asymmetric synthesis of 2,3-dihydroquinolin-4-one derivatives catalyzed by a chiral bisguanidium salt. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 15922-6. PMID 23154811 DOI: 10.1002/Chem.201203216 |
0.709 |
|
| 2012 |
Li J, Cai Y, Chen W, Liu X, Lin L, Feng X. Highly enantioselective fluorination of unprotected 3-substituted oxindoles: one-step synthesis of BMS 204352 (MaxiPost). The Journal of Organic Chemistry. 77: 9148-55. PMID 23030737 DOI: 10.1021/Jo301705T |
0.749 |
|
| 2012 |
Li W, Liu X, Hao X, Cai Y, Lin L, Feng X. A catalytic asymmetric ring-expansion reaction of isatins and α-alkyl-α-diazoesters: highly efficient synthesis of functionalized 2-quinolone derivatives. Angewandte Chemie (International Ed. in English). 51: 8644-7. PMID 22821752 DOI: 10.1002/Anie.201204594 |
0.755 |
|
| 2012 |
Cai Y, Li J, Chen W, Xie M, Liu X, Lin L, Feng X. Catalytic asymmetric sulfenylation of unprotected 3-substituted oxindoles. Organic Letters. 14: 2726-9. PMID 22587589 DOI: 10.1021/Ol3009446 |
0.749 |
|
| 2011 |
Cai Y, Liu X, Li J, Chen W, Wang W, Lin L, Feng X. Asymmetric iodoamination of chalcones and 4-aryl-4-oxobutenoates catalyzed by a complex based on scandium(III) and a N,N'-dioxide ligand. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 14916-21. PMID 22161911 DOI: 10.1002/Chem.201102453 |
0.713 |
|
| 2011 |
Chen W, Cai Y, Fu X, Liu X, Lin L, Feng X. Enantioselective one-pot synthesis of 2-amino-4-(indol-3-yl)-4H-chromenes. Organic Letters. 13: 4910-3. PMID 21859119 DOI: 10.1021/Ol2019949 |
0.724 |
|
| 2011 |
Cai Y, Liu X, Jiang J, Chen W, Lin L, Feng X. Catalytic asymmetric chloroamination reaction of α,β-unsaturated γ-keto esters and chalcones. Journal of the American Chemical Society. 133: 5636-9. PMID 21443187 DOI: 10.1021/Ja110668C |
0.648 |
|
| 2011 |
Jiang J, Cai Y, Chen W, Lin L, Liu X, Feng X. Enantioselective aza-Michael reaction of hydrazide to chalcones through the nonactivated amine moiety conjugated addition. Chemical Communications (Cambridge, England). 47: 4016-8. PMID 21344091 DOI: 10.1039/C0Cc05804A |
0.741 |
|
| 2011 |
Chen W, Cai Y, Fu X, Liu X, Lin L, Feng X. ChemInform Abstract: Enantioselective One-Pot Synthesis of 2-Amino-4-(indol-3-yl)-4H-chromenes. Cheminform. 43: no-no. DOI: 10.1002/chin.201203126 |
0.587 |
|
| 2011 |
Hui Y, Chen W, Wang W, Jiang J, Cai Y, Lin L, Liu X, Feng X. ChemInform Abstract: Highly Enantioselective Zinc-Catalyzed Friedel-Crafts Alkylation of Indoles with Ethyl Trifluoropyruvate. Cheminform. 42: no-no. DOI: 10.1002/chin.201118098 |
0.76 |
|
| 2010 |
Cai Y, Liu X, Hui Y, Jiang J, Wang W, Chen W, Lin L, Feng X. Catalytic asymmetric bromoamination of chalcones: highly efficient synthesis of chiral alpha-bromo-beta-amino ketone derivatives. Angewandte Chemie (International Ed. in English). 49: 6160-4. PMID 20648504 DOI: 10.1002/Anie.201002355 |
0.729 |
|
| 2010 |
Hui Y, Jiang J, Wang W, Chen W, Cai Y, Lin L, Liu X, Feng X. Highly enantioselective conjugate addition of thioglycolate to chalcones catalyzed by lanthanum: low catalyst loading and remarkable chiral amplification. Angewandte Chemie (International Ed. in English). 49: 4290-3. PMID 20449860 DOI: 10.1002/Anie.201000105 |
0.738 |
|
| 2010 |
Cai Y, Wang W, Shen K, Wang J, Hu X, Lin L, Liu X, Feng X. Highly enantioselective alpha-chlorination of cyclic beta-ketoesters catalyzed by N,N'-dioxide using NCS as the chlorine source. Chemical Communications (Cambridge, England). 46: 1250-2. PMID 20449266 DOI: 10.1039/B922769E |
0.687 |
|
| 2010 |
Feng X, Cai Y, Liu X, Hui Y, Jiang J, Wang W, Chen W, Lin L. Catalytic Asymmetric Bromoamination of Chalcones Synfacts. 2010: 1261-1261. DOI: 10.1055/S-0030-1258751 |
0.645 |
|
| 2010 |
Feng X, Hui Y, Jiang J, Wang W, Chen W, Cai Y, Lin L, Liu X. Catalytic Asymmetric Conjugate Addition of Thioglycolate to Chalcones Synfacts. 2010: 1025-1025. DOI: 10.1055/S-0030-1257943 |
0.668 |
|
| 2010 |
Chen W, Hui Y, Zhou X, Jiang J, Cai Y, Liu X, Lin L, Feng X. Chiral N,N′-dioxide-Yb(III) complexes catalyzed enantioselective hydrophosphonylation of aldehydes Tetrahedron Letters. 51: 4175-4178. DOI: 10.1016/J.Tetlet.2010.05.137 |
0.779 |
|
| 2010 |
Chen W, Hui Y, Zhou X, Jiang J, Cai Y, Liu X, Lin L, Feng X. ChemInform Abstract: Chiral N,N′-Dioxide-Yb(III) Complexes Catalyzed Enantioselective Hydrophosphonylation of Aldehydes. Cheminform. 41: no-no. DOI: 10.1002/chin.201048171 |
0.762 |
|
| 2010 |
Cai Y, Wang W, Shen K, Wang J, Hu X, Lin L, Liu X, Feng X. ChemInform Abstract: Highly Enantioselective α-Chlorination of Cyclic β-Ketoesters Catalyzed by N,N′-Dioxide Using NCS as the Chlorine Source. Cheminform. 41: no-no. DOI: 10.1002/chin.201026025 |
0.584 |
|
| 2010 |
Hui Y, Chen W, Wang W, Jiang J, Cai Y, Lin L, Liu X, Feng X. Highly Enantioselective Zinc-Catalyzed Friedel-Crafts Alkylation of Indoles with Ethyl Trifluoropyruvate Advanced Synthesis & Catalysis. 352: 3174-3178. DOI: 10.1002/Adsc.201000643 |
0.765 |
|
| 2009 |
Shen K, Liu X, Cai Y, Lin L, Feng X. Facile and efficient enantioselective Strecker reaction of ketimines by chiral sodium phosphate. Chemistry (Weinheim An Der Bergstrasse, Germany). 15: 6008-14. PMID 19418513 DOI: 10.1002/Chem.200900210 |
0.748 |
|
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