Year |
Citation |
Score |
2023 |
Chen P, Lv MJ, Cheng JK, Xiang SH, Ren XZ, Zhang J, Tan B. Enantioselective construction of triaryl-substituted all-carbon quaternary stereocenters organocatalytic arylation of oxindoles with azonaphthalenes. Chemical Science. 14: 2330-2335. PMID 36873834 DOI: 10.1039/d2sc07103g |
0.347 |
|
2022 |
Qiu SQ, Chen Y, Peng XJ, He SJ, Cheng JK, Wang YB, Xiang SH, Song J, Yu P, Zhang JM, Tan B. Asymmetric Construction of Aryl-Alkene Axis by Palladium-Catalyzed Suzuki-Miyaura Coupling Reaction. Angewandte Chemie (International Ed. in English). PMID 36111538 DOI: 10.1002/anie.202211211 |
0.371 |
|
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 |
0.66 |
|
2021 |
Yang J, Zhang JW, Bao W, Qiu SQ, Li S, Xiang SH, Song J, Zhang J, Tan B. Chiral Phosphoric Acid-Catalyzed Remote Control of Axial Chirality at Boron-Carbon Bond. Journal of the American Chemical Society. PMID 34384026 DOI: 10.1021/jacs.1c05079 |
0.321 |
|
2021 |
Jin J, Huang X, Xu J, Li T, Peng X, Zhu X, Zhang J, Jin Z, Chi YR. Carbene-Catalyzed Atroposelective Annulation and Desymmetrization of Urazoles. Organic Letters. PMID 33979174 DOI: 10.1021/acs.orglett.1c01191 |
0.598 |
|
2021 |
Xie Y, Yang X, Xu J, Chai H, Liu H, Zhang J, Song J, Gao Y, Jin Z, Chi YR. Access to Allene-Containing Molecules via Enantioselective Reactions of Azolium Cumulenolate Intermediates. Angewandte Chemie (International Ed. in English). PMID 33834597 DOI: 10.1002/anie.202102177 |
0.585 |
|
2020 |
Li Z, Ma P, Tan Y, Liu Y, Gao M, Zhang Y, Yang B, Huang X, Gao Y, Zhang J. Photocatalyst- and transition-metal-free α-allylation of N-aryl tetrahydroisoquinolines mediated by visible light Green Chemistry. 22: 646-650. DOI: 10.1039/C9Gc04191E |
0.338 |
|
2020 |
Wang K, Liang G, Waqas M, Yang B, Xiao K, Zhu C, Zhang J. Peroxymonosulfate enhanced photoelectrocatalytic degradation of ofloxacin using an easily coated cathode Separation and Purification Technology. 236: 116301. DOI: 10.1016/J.Seppur.2019.116301 |
0.311 |
|
2020 |
Liang G, Waqas M, Yang B, Xiao K, Li J, Zhu C, Zhang J, Duan H. Enhanced photocatalytic hydrogen evolution under visible light irradiation by p-type MoS2/n-type Ni2P doped g-C3N4 Applied Surface Science. 504: 144448. DOI: 10.1016/J.Apsusc.2019.144448 |
0.325 |
|
2019 |
Wei L, Zhou B, Xiao K, Yang B, Yu G, Li J, Zhu C, Zhang J, Duan H. Highly efficient degradation of 2,2',4,4'-tetrabromodiphenyl ether through combining surfactant-assisted Zn reduction with subsequent Fenton oxidation. Journal of Hazardous Materials. 121551. PMID 31708290 DOI: 10.1016/J.Jhazmat.2019.121551 |
0.353 |
|
2019 |
Liang H, Xiao K, Wei L, Yang B, Yu G, Deng S, Duan H, Zhu C, Li J, Zhang J. Decomplexation removal of Ni(II)-citrate complexes through heterogeneous Fenton-like process using novel CuO-CeO-CoO composite nanocatalyst. Journal of Hazardous Materials. 374: 167-176. PMID 30999140 DOI: 10.1016/J.Jhazmat.2019.04.031 |
0.373 |
|
2019 |
Xiao K, Liang H, Chen S, Yang B, Zhang J, Li J. Enhanced photoelectrocatalytic degradation of bisphenol A and simultaneous production of hydrogen peroxide in saline wastewater treatment. Chemosphere. 222: 141-148. PMID 30703653 DOI: 10.1016/J.Chemosphere.2019.01.109 |
0.332 |
|
2018 |
Huang Y, Xin Z, Yao W, Hu Q, Li Z, Xiao L, Yang B, Zhang J. A recyclable self-assembled composite catalyst consisting of FeO-rose bengal-layered double hydroxides for highly efficient visible light photocatalysis in water. Chemical Communications (Cambridge, England). PMID 30444510 DOI: 10.1039/C8Cc08130A |
0.672 |
|
2018 |
Wei T, Waqas M, Xiao K, Yang B, Luo Y, Luo Q, Zhang J, Wang M, Zhu C, He T, Lu Z. Effective degradation of refractory nitrobenzene in water by the natural 4-hydroxycoumarin under solar illumination. Chemosphere. 215: 199-205. PMID 30317090 DOI: 10.1016/J.Chemosphere.2018.10.034 |
0.357 |
|
2018 |
Zhang T, Liang W, Huang Y, Li X, Liu Y, Yang B, He C, Zhou X, Zhang J. Correction: Bifunctional organic sponge photocatalyst for efficient cross-dehydrogenative coupling of tertiary amines to ketones. Chemical Communications (Cambridge, England). PMID 30151529 DOI: 10.1039/c8cc90374c |
0.651 |
|
2018 |
Liang W, Zhang T, Liu Y, Huang Y, Liu Z, Liu Y, Yang B, Zhou X, Zhang J. Polydimethylsiloxane Sponge Supported Nanometer Gold: Highly Efficient Recyclable Catalyst for Cross-Dehydrogenative Coupling in Water. Chemsuschem. PMID 30125475 DOI: 10.1002/Cssc.201801180 |
0.71 |
|
2018 |
Xiao L, Huang Y, Luo Y, Yang B, Liu Y, Zhou X, Zhang J. Organic Cotton Photocatalysis Acs Sustainable Chemistry & Engineering. 6: 14759-14766. DOI: 10.1021/Acssuschemeng.8B03308 |
0.696 |
|
2018 |
Luo Y, Xie W, Huang Y, Zhang T, Yang B, Liu Y, Zhou X, Zhang J. Polydimethylsiloxane sponge supported DMAP on polymer brushes: Highly efficient recyclable base catalyst and ligand in water Journal of Catalysis. 367: 264-268. DOI: 10.1016/J.Jcat.2018.09.015 |
0.699 |
|
2017 |
Zhang Y, Zhao Y, Luo Y, Xiao L, Huang Y, Li X, Peng Q, Liu Y, Yang B, Zhu C, Zhou X, Zhang J. Directed Aromatic C-H Activation/Acetoxylation Catalyzed by Pd Nanoparticles Supported on Graphene Oxide. Organic Letters. 19: 6470-6473. PMID 29199835 DOI: 10.1021/Acs.Orglett.7B02967 |
0.69 |
|
2017 |
Zhang T, Liang W, Huang Y, Li X, Liu Y, Yang B, He C, Zhou X, Zhang J. Bifunctional organic sponge photocatalyst for efficient cross-dehydrogenative coupling of tertiary amines to ketones. Chemical Communications (Cambridge, England). PMID 29109986 DOI: 10.1039/C7Cc06997A |
0.697 |
|
2017 |
He T, Li J, Li X, Ren C, Luo Y, Zhao F, Chen R, Lin X, Zhang J. Spectroscopic studies of chiral perovskite nanocrystals Applied Physics Letters. 111: 151102. DOI: 10.1063/1.5001151 |
0.304 |
|
2017 |
Liu Z, Yang Z, Huang X, Xuan C, Xie J, Fu H, Wu Q, Zhang J, Zhou X, Liu Y. High-absorption recyclable photothermal membranes used in a bionic system for high-efficiency solar desalination via enhanced localized heating Journal of Materials Chemistry. 5: 20044-20052. DOI: 10.1039/C7Ta06384A |
0.312 |
|
2017 |
Li X, Li Y, Huang Y, Zhang T, Liu Y, Yang B, He C, Zhou X, Zhang J. Organic sponge photocatalysis Green Chemistry. 19: 2925-2930. DOI: 10.1039/C6Gc03558B |
0.701 |
|
2016 |
Lin Z, Zhang J, Gao Y. An Efficient Synthesis of Tetracyclic Pyrano[2,3-d]pyrimidines Journal of Heterocyclic Chemistry. 54: 596-602. DOI: 10.1002/Jhet.2630 |
0.408 |
|
2013 |
Zhang J, Xing C, Tiwari B, Chi YR. Catalytic activation of carbohydrates as formaldehyde equivalents for Stetter reaction with enones. Journal of the American Chemical Society. 135: 8113-6. PMID 23688031 DOI: 10.1021/Ja401511R |
0.751 |
|
2012 |
Zhang J, Tiwari B, Xing C, Chen X, Chi YR. Enantioselective oxidative cross-dehydrogenative coupling of tertiary amines to aldehydes. Angewandte Chemie (International Ed. in English). 51: 3649-52. PMID 22389195 DOI: 10.1002/Anie.201109054 |
0.756 |
|
2012 |
Tiwari B, Zhang J, Chi YR. Facile access to chiral ketones through metal-free oxidative C-C bond cleavage of aldehydes by O2. Angewandte Chemie (International Ed. in English). 51: 1911-4. PMID 22253214 DOI: 10.1002/Anie.201107473 |
0.717 |
|
2011 |
Xing C, Sun H, Zhang J, Li G, Chi YR. Brønsted acid catalyzed α-alkylation of aldehydes with diaryl methyl alcohols. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 12272-5. PMID 21932270 DOI: 10.1002/Chem.201102623 |
0.61 |
|
2011 |
Li XM, Wang B, Zhang JM, Yan M. Asymmetric organocatalytic double-conjugate addition of malononitrile to dienones: efficient synthesis of optically active cyclohexanones. Organic Letters. 13: 374-7. PMID 21188969 DOI: 10.1021/Ol102570B |
0.536 |
|
2011 |
Li X, Wang B, Zhang J, Yan M. ChemInform Abstract: Asymmetric Organocatalytic Double-Conjugate Addition of Malononitrile to Dienones: Efficient Synthesis of Optically Active Cyclohexanones. Cheminform. 42: no-no. DOI: 10.1002/chin.201119059 |
0.403 |
|
2010 |
Hu Z, Zhang J, Lou C, Wang J, Nie S, Yan aM. Efficient conjugate addition of carbonyl compounds to3-nitro-2H-chromenes in the presence of bases Arkivoc. 2010. DOI: 10.3998/Ark.5550190.0011.A03 |
0.422 |
|
2009 |
Xuan YN, Nie SZ, Dong LT, Zhang JM, Yan M. Highly enantioselective synthesis of nitrocyclopropanes via organocatalytic conjugate addition of bromomalonate to alpha,beta-unsaturated nitroalkenes. Organic Letters. 11: 1583-6. PMID 19260703 DOI: 10.1021/Ol900227J |
0.539 |
|
2009 |
Yan M, Dong L, Du Q, Lou C, Zhang J, Lu R. Asymmetric Synthesis of Nitrocyclopropanes Catalyzed by Chiral Primary Amines Synlett. 2010: 266-270. DOI: 10.1055/S-0029-1218570 |
0.559 |
|
2009 |
Zhang J, Hu Z, Dong L, Xuan Y, Lou C, Yan M. Enantioselective conjugate addition of 1-bromonitroalkanes to α,β-unsaturated aldehydes catalyzed by chiral secondary amines Tetrahedron: Asymmetry. 20: 355-361. DOI: 10.1016/J.Tetasy.2009.01.003 |
0.546 |
|
2009 |
Dong L, Lu R, Du Q, Zhang J, Liu S, Xuan Y, Yan M. Highly enantioselective conjugate addition of 1-bromonitroalkanes to α,β-unsaturated ketones catalyzed by 9-amino-9-deoxyepiquinine Tetrahedron. 65: 4124-4129. DOI: 10.1016/J.Tet.2009.03.055 |
0.532 |
|
2009 |
Zhang J, Hu Z, Zhao S, Yan M. Organocatalytic conjugate addition of 1-bromonitroalkanes to α,β-unsaturated aldehydes: synthesis of nitrocyclopropanes Tetrahedron. 65: 802-806. DOI: 10.1016/J.Tet.2008.11.060 |
0.549 |
|
2009 |
Zhang J, Hu Z, Dong L, Xuan Y, Lou C, Yan M. ChemInform Abstract: Enantioselective Conjugate Addition of 1-Bromonitroalkanes to α,β-Unsaturated Aldehydes Catalyzed by Chiral Secondary Amines. Cheminform. 40. DOI: 10.1002/chin.200934046 |
0.393 |
|
2009 |
Xuan Y, Nie S, Dong L, Zhang J, Yan M. ChemInform Abstract: Highly Enantioselective Synthesis of Nitrocyclopropanes via Organocatalytic Conjugate Addition of Bromomalonate to α,β-Unsaturated Nitroalkenes. Cheminform. 40. DOI: 10.1002/chin.200933060 |
0.368 |
|
2009 |
Zhang J, Hu Z, Zhao S, Yan M. ChemInform Abstract: Organocatalytic Conjugate Addition of 1-Bromonitroalkanes to α,β-Unsaturated Aldehydes: Synthesis of Nitrocyclopropanes. Cheminform. 40. DOI: 10.1002/chin.200922061 |
0.353 |
|
2008 |
ZHANG S, ZHANG J. Ytterbium(III) Triflate as an Efficient Catalyst for the Synthesis of Perimidine Derivatives under Mild Conditions Chinese Journal of Chemistry. 26: 185-189. DOI: 10.1002/Cjoc.200890019 |
0.496 |
|
2008 |
Zhang J, Zhang SL, Zhang JM. ChemInform Abstract: Ruthenium(III) Chloride as an Efficient Catalyst for the Synthesis of Perimidine Derivatives under Mild Conditions. Cheminform. 39. DOI: 10.1002/CHIN.200822166 |
0.32 |
|
2008 |
Zhang S, Zhang J. ChemInform Abstract: Ytterbium(III) Triflate as an Efficient Catalyst for the Synthesis of Perimidine Derivatives under Mild Conditions. Cheminform. 39. DOI: 10.1002/CHIN.200819152 |
0.315 |
|
2007 |
Zhang J, Zhang S. Bismuth(III) Chloride–Promoted Efficient Synthesis of Perimidine Derivatives under Ambient Conditions Synthetic Communications. 37: 2615-2624. DOI: 10.1080/00397910701463011 |
0.436 |
|
2007 |
Zhang J, Zhang SL, Zhang JM. Ruthenium(III) chloride as an efficient catalyst for the synthesis of perimidine derivatives under mild conditions Chinese Chemical Letters. 18: 1057-1060. DOI: 10.1016/J.Cclet.2007.07.004 |
0.493 |
|
2006 |
Li Y, Zhang J, Dong L, Yan M. Imino Diels-Alder Reaction Catalyzed by Iodine: Efficient Synthesis of Tetrahydroquinolines Chinese Journal of Chemistry. 24: 929-932. DOI: 10.1002/Cjoc.200690176 |
0.581 |
|
2006 |
Li Y, Zhang J, Dong L, Yan M. Imino Diels—Adler Reaction Catalyzed by Iodine: Efficient Synthesis of Tetrahydroquinolines. Cheminform. 37. DOI: 10.1002/chin.200647156 |
0.501 |
|
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