{"id":12108,"date":"2023-10-18T10:22:33","date_gmt":"2023-10-18T14:22:33","guid":{"rendered":"http:\/\/149.4.100.129\/academics\/chem\/?page_id=12108"},"modified":"2025-03-07T16:13:31","modified_gmt":"2025-03-07T21:13:31","slug":"yu-chen-publications","status":"publish","type":"page","link":"https:\/\/www.qc.cuny.edu\/academics\/chem\/yu-chen-publications\/","title":{"rendered":"Publications"},"content":{"rendered":"

[et_pb_section fb_built=”1″ fullwidth=”on” _builder_version=”4.22.2″ _module_preset=”default” global_colors_info=”{}”][et_pb_fullwidth_image src=”https:\/\/www.qc.cuny.edu\/academics\/chem\/wp-content\/uploads\/sites\/32\/2023\/10\/aerial-shot-clock-tower-QC.jpg” title_text=”aerial-shot-clock-tower-QC” _builder_version=”4.22.2″ _module_preset=”default” global_colors_info=”{}”][\/et_pb_fullwidth_image][et_pb_fullwidth_header title=”Dr. Yu Chen” subhead=”Professor” _builder_version=”4.27.4″ _module_preset=”default” title_font_size=”45px” content_font_size=”16px” subhead_font_size=”25px” background_color=”#E71939″ global_colors_info=”{}”]<\/p>\n

Department of Chemistry and Biochemistry<\/p>\n

[\/et_pb_fullwidth_header][\/et_pb_section][et_pb_section fb_built=”1″ _builder_version=”4.27.4″ _module_preset=”default” global_colors_info=”{}”][et_pb_row column_structure=”1_4,3_4″ _builder_version=”4.27.4″ _module_preset=”default” global_colors_info=”{}”][et_pb_column type=”1_4″ _builder_version=”4.22.2″ _module_preset=”default” global_colors_info=”{}”][et_pb_text _builder_version=”4.22.2″ _module_preset=”default” global_colors_info=”{}”]<\/p>\n

Home<\/a>
\nResearch<\/a>
\nPublications<\/a>
\nGroup Members<\/a>
\nGallery<\/a><\/div>\n

[\/et_pb_text][\/et_pb_column][et_pb_column type=”3_4″ _builder_version=”4.22.2″ _module_preset=”default” global_colors_info=”{}”][dsm_text_divider header=”Chen Group Publications” text_alignment=”left” color=”#333333″ _builder_version=”4.27.4″ _module_preset=”default” header_font=”Open Sans|600|||||||” global_colors_info=”{}”][\/dsm_text_divider][et_pb_text admin_label=”Text” _builder_version=”4.27.4″ _module_preset=”default” text_font=”Open Sans||||||||” text_font_size=”16px” header_4_font=”Open Sans|600|||on||||” header_4_text_color=”#000000″ global_colors_info=”{}”]<\/p>\n

24) Yang, W.; Guo, J.; Hee, S.; Chen. Y.* \u201cRecent Advances in Iodine-Mediated Radical Reactions\u201d, Adv. Synth. Catal.<\/em> 2025<\/strong>, 367<\/em>, e202401486. https:\/\/doi.org\/10.1002\/adsc.202401486<\/a><\/span><\/span><\/p>\n

23) Liu, X.; Hee, S.; Sapir, N. G.; Li, A.; Farkruzzaman, S.; Liu, J.;* Chen, Y.* \u201cn<\/em>-Bu4<\/sub>NI\/K2<\/sub>S2<\/sub>O8<\/sub> Mediated C\u2013N Coupling between Aldehydes and Amides\u201d, Eur. J. Org. Chem.<\/em> 2024<\/strong>, 27, e202400067. https:\/\/doi.org\/10.1002\/ejoc.202400067<\/a><\/span><\/p>\n

22) Liu, X.; Hee, S.; Sapir, N. G.; Li, A.; Liu, J.;* Chen, Y.* <\/sup>\u201cn<\/em>-Bu4<\/sub>NI\/K2<\/sub>S2<\/sub>O8<\/sub>-Mediated Csp2<\/sup>-Csp2<\/sup> Bond Cleavage \u2013 Transformylation from p<\/em>-Anisaldehyde to Primary Amides\u201d, Adv. Synth. Catal.<\/em> 2024<\/strong>, 366<\/em>, 2489-2494. https:\/\/doi.org\/10.1002\/adsc.202301505<\/a><\/span><\/p>\n

21) Ghosh, P.;* Chhetri, G.; Mandal, A.; Chen, Y.; Hersh, W. H.; Das, S.* \u201cC(sp2<\/sup>)\u2013H selenylation of substituted benzo[4,5] imidazo[2,1-b<\/em>]thiazoles using phenyliodine(III) bis(trifluoroacetate) as a mediator\u201d, RSC Adv.<\/em> 2024<\/strong>, 14<\/em>, 4462\u20134470. https:\/\/doi.org\/10.1039\/D4RA00057A<\/a><\/span><\/p>\n

20) Barman, K.; Chen, Y.; Wu, S.; Hu, G.;* Mirkin, M. V.* \u201cVoltage-Driven Molecular Catalysis: A Promising Approach to Electrosynthesis\u201d, ACS Catal.<\/em> 2023<\/strong>, 13<\/em>, 15869-15876. https:\/\/doi.org\/10.1021\/acscatal.3c03644<\/a><\/span><\/p>\n

19) Chen, Y.;* Hee, S.; Liu, X.; Das, S.; Hong, D.; <\/sup>Leung, P.-H.; Li, Y.; <\/sup>Li, J.; Liu, J.* \u201cICl-Mediated Functional Group Interconversion from Methyl Homopropargyl Ether to \u03b1-Iodo-\u03b3-chloroketone\u201d, J. Org. Chem.<\/em> 2022<\/strong>, 87<\/em>, 15129\u221215138. https:\/\/doi.org\/10.1021\/acs.joc.2c01638<\/a><\/span><\/p>\n

18) Domaradzki, M. E.; Liu, X.; Ong, J.; Yu, G.; Zhang, G.; Simantov, A.; Perl, E.; Chen, Y.* \u201cTriflic Acid Mediated Sequential Cyclization of ortho-Alkynylarylesters with Ammonium Acetate\u201d, Tetrahedron<\/em> 2020<\/strong>, 76<\/em>, 131437. https:\/\/doi.org\/10.1016\/j.tet.2020<\/a><\/p>\n

17) Yang, W.; Liu, X.; Leung, P.-H.; Li, Y.; Yang, D.; Chen, Y.* \u201cIron-Mediated Ring-Opening and Rearrangement Cascade Synthesis of Polysubstituted Pyrroles from 4-Alkenylisoxazoles\u201d, Adv. Synth. Catal.<\/em> 2020<\/strong>, 362<\/em>, 1868-1876. https:\/\/doi.org\/10.1002\/adsc.201901649<\/a><\/p>\n

16) Liu, X.; Hong, D.; Sapir, N. G.; Yang, W.; Hersh, W. H.; Leung, P.-H.; Yang, D.; Chen, Y.* \u201cIron-\u200bCatalyzed Transfer Hydrogenation in Aged N-\u200bMethyl-\u200b2-\u200bpyrrolidone: Reductive Ring-\u200bOpening of 3,\u200b5-\u200bDisubstituted Isoxazoles and Isoxazolines\u201d, J. Org. Chem.<\/em> 2019<\/strong>, 84<\/em>, 16204-16213. https:\/\/doi.org\/10.1021\/acs.joc.9b02733<\/a><\/p>\n

15) Yang, W.; Chen, Y.; Yao, Y.; Lin, Q.; Yang, D.* \u201cIron-\u200bPromoted Reductive Ring-\u200bOpening and Isomerization Reactions of C4-\u200bAlkynylisoxazoles Leading to 2-\u200bAlkynylenaminones and Polysubstituted Furans\u201d, Adv. Synth. Catal.<\/em> 2019<\/strong>, 361<\/em>, 5634-5642. https:\/\/doi.org\/10.1002\/adsc.201901176<\/a><\/p>\n

14) Li, X.-R.; Chen, H. J.; Wang, W.; Ma, M.; Chen, Y.; Li, Y.; Pullarkat, S. A.; Leung, P.-H.* \u201cPalladacycle promoted asymmetric hydrophosphination of \u03b1,\u03b2-unsaturated sulfonylfluorides\u201d, J. Organomet. Chem.<\/em> 2019<\/strong>, 899<\/em>, 120912. https:\/\/doi.org\/10.1016\/j.jorganchem.2019.120912<\/a><\/p>\n

13) Yang. W.; Chen, Y.; Yao, Y.; Yang, X.; Lin, Q.; Yang, D.* \u201cICl\/AgNO3 Co-Catalyzed Radical Oxidation of Diaryl- and Alkylarylalkynes into 1,2-Diketones\u201d, J. Org. Chem.<\/em> 2019<\/strong>, 84<\/em>, 11080-11090. https:\/\/doi.org\/10.1021\/acs.joc.9b01667<\/a><\/p>\n

12) Li, X. R.; Chen, Y.; Pang, B. P.; Tan, J.; Li, Y.; Pullarkat, S. A.; Leung, P.-H.* \u201cEfficient Synthesis of Malonate Functionalized Chiral Phosphapalladacycles and their Catalytic Evaluation in Asymmetric Hydrophosphination of Chalcone\u201d, Eur. J. Inorg. Chem.<\/em> 2018<\/strong>, 4385\u20134390. https:\/\/doi.org\/10.1002\/ejic.201800720<\/a><\/p>\n

11) Liu, X.; Hong, D.; She, Z.; Hersh, W. H.; Yoo, B.; Chen, Y.* \u201cComplementary regioselective synthesis of 3,5-disubstituted isoxazoles from ynones\u201d, Tetrahedron<\/em> 2018<\/strong>, 74<\/em>, 6593-6606. https:\/\/doi.org\/10.1016\/j.tet.2018.09.043<\/a><\/p>\n

10) Wang, S.; Jia, K.; Cheng, J.; Chen, Y.;* Yuan, Y.* \u201cDual roles of substituted thiourea as reductant and ligand in CuAAC reaction\u201d, Tetrahedron Lett.<\/em>\u00a02017<\/strong>, 58<\/em>, 3717-3721. https:\/\/doi.org\/10.1016\/j.tetlet.2017.08.029<\/a><\/p>\n

9) Ouyang, J.; Su, X.; Chen, Y.; Yuan, Y.;* Li, Y.* \u201cCopper-Catalyzed Carbochlorination or Carbobromination via Radical Cyclization of Aryl Amines\u201d, Tetrahedron Lett.<\/em> 2016<\/strong>, 57<\/em>, 1438-1441. https:\/\/doi.org\/10.1016\/j.tetlet.2016.02.054<\/a><\/p>\n

8) Das, S.; Hong, D.; Chen, Z.; She, Z.; Hersh, W. H.; Subramaniam, G.; Chen, Y.* \u201cAuto-Tandem Palladium Catalysis: From Isoxazole to 2-Azafluorenone\u201d, Org. Lett.<\/em> 2015<\/strong>, 17<\/em>, 5578-5581. https:\/\/doi.org\/10.1021\/acs.orglett.5b02731<\/a><\/p>\n

7) Domaradzki, M. E.; Long, Y.; She, Z.; Liu, X.; Zhang, G.; Chen, Y.* \u201cGold-Catalyzed Ammonium Acetate-Assisted Cascade Cyclization of 2-Alkynylarylketones\u201d, J. Org. Chem.<\/em> 2015<\/strong>, 80<\/em>, 11360-11368. https:\/\/doi.org\/10.1021\/acs.joc.5b01939<\/a><\/p>\n

6) Chen, Y.;* Huang, C.; Liu, X.; Perl, E.; Chen, Z.; Namgung, J.; Subramaniam, G.; Zhang, G.; Hersh, W. H. \u201cSynthesis of Dibenzocyclohepten-5-ones by Electrophilic Iodocyclization of 1-([1,1′-Biphenyl]-2-yl)-alkynones\u201d, J. Org. Chem.<\/em> 2014<\/strong>, 79<\/em>, 3452-3464. https:\/\/doi.org\/10.1021\/jo5001803<\/a><\/p>\n

5) Chen, Y.;* Liu, X.; Lee, M.; Huang, C.; Inoyatov, I.; Chen, Z.; Perl, A. C.; Hersh, W. H. \u201cICl-Induced Intramolecular Electrophilic Cyclization of 1-(4′-Methoxy-[1,1′-biphenyl]-2-yl)-alkynones\u2014A Facile Approach to Spiroconjugated Molecules\u201d, Chem. Eur. J.<\/em> 2013<\/strong>, 19<\/em>, 9795-9799. https:\/\/doi.org\/10.1002\/chem.201301582<\/a><\/p>\n

4) Long, Y.; She, Z.; Liu, X.; Chen, Y.* \u201cSynthesis of 1-Aminoisoquinolines by Gold(III)-Mediated Domino Reactions from 2-Alkynylbenzamides and Ammonium Acetate\u201d, J. Org. Chem.<\/em> 2013<\/strong>, 78<\/em>, 2579-2588. https:\/\/doi.org\/10.1021\/jo302794z<\/a><\/p>\n

3) Yang, D.; Burugupalli, S.; Daniel, D.; Chen, Y.* \u201cMicrowave-Assisted One-Pot Synthesis of Isoquinolines, Furopyridines and Thienopyridines by Palladium-Catalyzed Sequential Coupling-Imination-Annulation of 2-Bromoarylaldehydes with Terminal Acetylenes and Ammonium Acetate\u201d, J. Org. Chem.<\/em> 2012<\/strong>, 77<\/em>, 4466-4472. [highlighted in SYNFACTS<\/em> \u201cOne-Pot Pd-Catalyzed Synthesis of Isoquinolines and Furo\/Thienopyridines.\u201dSYNFACTS <\/em>2012<\/strong>, 8<\/em>, 830.] https:\/\/doi.org\/10.1021\/jo300494a<\/a><\/p>\n

2) She, Z.; Niu, D.; Chen, L.; Gunawan, M. A.; Shanja, X.; Hersh, W. H.; Chen, Y.* “Synthesis of Trisubstituted Isoxazoles by Palladium(II)-Catalyzed Cascade Cyclization-Alkenylation of 2-Alkyn-1-one O-Methyl Oximes,” J. Org. Chem.<\/em> 2012<\/strong>, 77<\/em>, 3627\u22123633. https:\/\/doi.org\/10.1021\/jo300090k<\/a><\/p>\n

1) Long, Y.; Yang, D.;* Zhang, Z.; Wu, Y.; Zeng, H.; Chen, Y.* \u201cIridium-Catalyzed Asymmetric Ring-Opening of Azabicyclic Alkenes by Amines,\u201d J. Org. Chem.<\/em> 2010<\/strong>, 75<\/em>, 7291-7299. https:\/\/pubs.acs.org\/doi\/10.1021\/jo101470r<\/a><\/p>\n

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Department of Chemistry and BiochemistryHome Research Publications Group Members Gallery

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Chen Group Publications<\/span><\/h3>\n\t\t\t\t
<\/div>\n\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t<\/div>24) Yang, W.; Guo, J.; Hee, S.; Chen. Y.* \u201cRecent Advances in Iodine-Mediated Radical Reactions\u201d, Adv. Synth. Catal. 2025, 367, e202401486. https:\/\/doi.org\/10.1002\/adsc.202401486 23) Liu, X.; Hee, S.; Sapir, N. G.; Li, A.; Farkruzzaman, S.; Liu, J.;* […]<\/p>\n","protected":false},"author":197,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_et_pb_use_builder":"on","_et_pb_old_content":"","_et_gb_content_width":"","inline_featured_image":false,"footnotes":""},"page_category":[],"wf_page_folders":[282],"class_list":["post-12108","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/www.qc.cuny.edu\/academics\/chem\/wp-json\/wp\/v2\/pages\/12108","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.qc.cuny.edu\/academics\/chem\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/www.qc.cuny.edu\/academics\/chem\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/www.qc.cuny.edu\/academics\/chem\/wp-json\/wp\/v2\/users\/197"}],"replies":[{"embeddable":true,"href":"https:\/\/www.qc.cuny.edu\/academics\/chem\/wp-json\/wp\/v2\/comments?post=12108"}],"version-history":[{"count":0,"href":"https:\/\/www.qc.cuny.edu\/academics\/chem\/wp-json\/wp\/v2\/pages\/12108\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.qc.cuny.edu\/academics\/chem\/wp-json\/wp\/v2\/media?parent=12108"}],"wp:term":[{"taxonomy":"page_category","embeddable":true,"href":"https:\/\/www.qc.cuny.edu\/academics\/chem\/wp-json\/wp\/v2\/page_category?post=12108"},{"taxonomy":"wf_page_folders","embeddable":true,"href":"https:\/\/www.qc.cuny.edu\/academics\/chem\/wp-json\/wp\/v2\/wf_page_folders?post=12108"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}