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Liejin Zhou - Publications

Affiliations: 
Zhejiang Normal University, Jinhua Shi, Zhejiang Sheng, China 
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30 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 Wang Y, Jin Z, Zhou L, Lv X. Recent advances in [4 + 4] annulation of conjugated heterodienes with 1,4-dipolar species for the synthesis of eight-membered heterocycles. Organic & Biomolecular Chemistry. PMID 38062977 DOI: 10.1039/d3ob01626a  0.422
2023 Zhang B, Jin Z, Huang C, Zhang Y, Shen G, Kang H, Lv X, Zhou L. Highly Diastereoselective One-Pot Synthesis of 4,5-Dihydrofuro[2,3-]azocin-6-one Derivatives through Cyclization/[4+4] Annulation Reactions. The Journal of Organic Chemistry. PMID 37155326 DOI: 10.1021/acs.joc.3c00003  0.605
2023 Wei S, Zhang G, Wang Y, You M, Wang Y, Zhou L, Zhang Z. Modular synthesis of unsaturated aza-heterocycles via copper catalyzed multicomponent cascade reaction. Iscience. 26: 106137. PMID 36895640 DOI: 10.1016/j.isci.2023.106137  0.563
2022 Yang X, Wei L, Wu Y, Zhou L, Zhang X, Chi YR. Atroposelective Access to 1,3-Oxazepine-Containing Bridged Biaryls via Carbene-Catalyzed Desymmetrization of Imines. Angewandte Chemie (International Ed. in English). PMID 36087019 DOI: 10.1002/anie.202211977  0.674
2022 Wang X, Yu J, Xu M, Mao H, Shan Y, Lv X, Zhou L. Metal-Free [5 + 1] Cycloaddition-Aromatization of Benzotriazoles and Sulfur Ylides to Construct 1,2,4-Benzotriazines. Organic Letters. PMID 35929849 DOI: 10.1021/acs.orglett.2c02064  0.385
2022 Lei Z, Wei S, Zhou L, Zhang Z, Lopez SE, Dolbier WR. Photocatalytic difluoromethylarylation of unactivated alkenes a (hetero)aryl neophyl-like radical migration. Organic & Biomolecular Chemistry. PMID 35838250 DOI: 10.1039/d2ob00813k  0.588
2022 Zhang B, Yu J, Wu X, Chai Z, Zhao G, Li Z, Kang H, Lv X, Zhou L. Synthesis of Furo[2,3-][1,4]diazepin-3-one Derivatives through Tandem Cyclization/[4 + 3] Annulation Reactions. The Journal of Organic Chemistry. PMID 35076248 DOI: 10.1021/acs.joc.1c02561  0.55
2021 Ye Z, Lei Z, Ye X, Zhou L, Wang Y, Yuan Z, Gao F, Britton R. Decatungstate Catalyzed Synthesis of Trifluoromethylthioesters from Aldehydes via a Radical Process. The Journal of Organic Chemistry. PMID 34882428 DOI: 10.1021/acs.joc.1c02244  0.345
2021 Zhou L, Liu L. Highly enantioselective tandem cycloisomerization/Diels-Alder reaction of 2-(1-alkynyl)-2-alken-1-ones and enals: dual catalysis with platinum and amines. Chemical Communications (Cambridge, England). PMID 33982035 DOI: 10.1039/d1cc02080c  0.659
2021 Zhang Z, Zhou L, Wei S, Lei Z, Zhu G. Transition-Metal-Free α Csp3-H Cyanation of Sulfonamides. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 33769613 DOI: 10.1002/chem.202100902  0.309
2021 Yang X, Xie Y, Xu J, Ren S, Mondal B, Zhou L, Tian W, Zhang X, Hao L, Jin Z, Chi YR. Carbene-Catalyzed Activation of Remote Nitrogen Atoms of (benz)imidazole-derived aldimines for Enantioselective Synthesis of Heterocycles. Angewandte Chemie (International Ed. in English). PMID 33469976 DOI: 10.1002/anie.202016506  0.726
2020 Yang X, Majhi PK, Chai H, Liu B, Sun J, Liu T, Liu Y, Zhou L, Xu J, Liu J, Wang D, Zhao Y, Jin Z, Chi YR. Carbene-Catalyzed Enantioselective Aldol Reaction: Post-Aldol Stereochemistry Control and Formation of Quaternary Stereogenic Centers. Angewandte Chemie (International Ed. in English). PMID 32931603 DOI: 10.1002/anie.202008369  0.75
2020 Mou C, Zhou L, Song R, Chai H, Hao L, Chi YR. Carbene-Catalyzed Reaction of Indolyl Methylenemalononitriles and Enals for Access to Complex Tetrahydrocarbazoles. Organic Letters. PMID 32191040 DOI: 10.1021/acs.orglett.0c00418  0.695
2020 Lin Y, Li E, Wu X, Wang L, Wang H, Li X, Kang H, Zhou L, Shen G, Lv X. One-pot synthesis of 2-azolylimidazole derivatives through a domino addition/A coupling/cyclization process under copper catalysis. Organic & Biomolecular Chemistry. PMID 32026913 DOI: 10.1039/c9ob02532d  0.342
2019 Zhou L, Wu X, Yang X, Mou C, Song R, Yu S, Chai H, Pan L, Jin Z, Chi YR. ---------------Gold and Carbene Relay Catalytic Enantioselective Cycloisomerization/Cyclization Reactions of Ynamides and Enals. Angewandte Chemie (International Ed. in English). PMID 31724277 DOI: 10.1002/anie.201910922  0.715
2019 Ke J, Wang H, Zhou L, Mou C, Zhang J, Pan L, Chi YR. Catalyst- and Metal-Free Hydrodehalogenation of Aryl Halides through Direct Electrolysis. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 30950097 DOI: 10.1002/chem.201901082  0.673
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  0.619
2018 Wu X, Zhou L, Maiti R, Mou C, Pan L, Chi YR. Sulfinate and Carbene Co-catalyzed Rauhut-Currier Reaction for Enantioselective Access to Azepino[1,2-a]indole. Angewandte Chemie (International Ed. in English). PMID 30398684 DOI: 10.1002/anie.201810879  0.739
2017 Mao H, You BX, Zhou LJ, Xie TT, Wen YH, Lv X, Wang XX. SmI2-mediated reductive cyclization of β-arylthio ketones: a facile and diastereoselective synthesis of thiochroman derivatives. Organic & Biomolecular Chemistry. PMID 28686268 DOI: 10.1039/c7ob01082f  0.343
2016 Li W, Zhou L, Zhang J. Recent Progress in Dehydro(genative) Diels-Alder Reaction. Chemistry (Weinheim An Der Bergstrasse, Germany). 22: 1558-71. PMID 26786814 DOI: 10.1002/Chem.201503571  0.528
2015 Zhou L, Xu B, Zhang J. Metal-Free Dehydrogenative Diels-Alder Reactions of 2-Methyl-3-Alkylindoles with Dienophiles: Rapid Access to Tetrahydrocarbazoles, Carbazoles, and Heteroacenes. Angewandte Chemie (International Ed. in English). PMID 26096824 DOI: 10.1002/Anie.201503549  0.306
2014 Zhou L, Zhang M, Li W, Zhang J. Furan-based o-quinodimethanes by gold-catalyzed dehydrogenative heterocyclization of 2-(1-alkynyl)-2-alken-1-ones: a modular entry to 2,3-furan-fused carbocycles. Angewandte Chemie (International Ed. in English). 53: 6542-5. PMID 24838396 DOI: 10.1002/Anie.201403709  0.382
2014 Zhou L, Zhang M, Li W, Zhang J. ChemInform Abstract: Furan-Based o-Quinodimethanes by Gold-Catalyzed Dehydrogenative Heterocyclization of 2-(1-Alkynyl)-2-alken-1-ones: A Modular Entry to 2,3-Furan-Fused Carbocycles. Cheminform. 45: no-no. DOI: 10.1002/CHIN.201449103  0.301
2013 Yin R, Zhou L, Liu H, Lue X, Mao H, Wang X. ChemInform Abstract: Reactivity of AllylSmBr/HMPA: Facile Synthesis of 3-Aryl-1,2,4-benzotriazines. Cheminform. 44: no-no. DOI: 10.1002/CHIN.201343181  0.394
2012 Tu Y, Zhou L, Yin R, Lv X, Flowers RA, Choquette KA, Liu H, Niu Q, Wang X. Study on the coupling of acyclic esters with alkenes--the synthesis of 2-(2-hydroxyalkyl)cyclopropanols via cascade cyclization using allylsamarium bromide. Chemical Communications (Cambridge, England). 48: 11026-8. PMID 23038019 DOI: 10.1039/C2Cc34630C  0.345
2012 Liu H, Lv X, Zhou L, Yin R, Wang X. Preparation of 2-heteroatom substituted 4-oxo-4-arylbutanoates via thio- and aza-Michael addition Journal of the Serbian Chemical Society. 77: 581-588. DOI: 10.2298/JSC110526202L  0.391
2012 Yin R, Zhou L, Liu H, Mao H, Lü X, Wang X. Reactivity of AllylSmBr/HMPA: Facile Synthesis of 3-Aryl-1,2,4-benzotriazines Chinese Journal of Chemistry. 31: 143-148. DOI: 10.1002/CJOC.201200989  0.407
2011 Lv X, Zhang Y, Zhou L, Wang X. Facile and efficient conjugate additions of β-dicarbonyl compounds and nitroalkanes to 4-aryl-4-oxobut-2-enoates Journal of the Serbian Chemical Society. 76: 947-954. DOI: 10.2298/JSC100909066L  0.335
2011 Zhou L, Lv X, Mao H, Wang X. Selective substitution reactions of methoxycarbonylamino-1-(1-benzotriazolyl)alkanes with active methylene compounds Journal of Heterocyclic Chemistry. 48: 434-440. DOI: 10.1002/JHET.612  0.407
2011 Zhou L, Lv X, Mao H, Wang X. ChemInform Abstract: Selective Substitution Reactions of Methoxycarbonylamino-1-(1-benzotriazolyl)alkanes with Active Methylene Compounds. Cheminform. 42: no-no. DOI: 10.1002/CHIN.201133116  0.414
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