Qiuling Song, Ph.D.
Affiliations: | 2012- | Chemical Engineering | Huaqiao University |
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"Qiuling Song"Mean distance: 8.57
Parents
Sign in to add mentorZhenfeng Xi | grad student | 1998-2001 | Peking University |
Robert Anthony Pascal Jr. | grad student | 2002-2007 | Princeton |
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Publications
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Wang Y, Huang X, Chen J, et al. (2025) Diastereoselective radical cascade cyclization to access indole-fused diazepine derivatives. Organic & Biomolecular Chemistry |
Yao T, Zhao C, Li C, et al. (2025) Photoinduced Assembly of Diverse Homoallylic Boronates from -Diborons. Organic Letters. 27: 2597-2601 |
Li W, Lu Y, Cheng S, et al. (2025) Synthesis of Polysubstituted Aromatics via the Pd(II)-Initiated Borono-Catellani Reaction. Organic Letters |
Mu S, Xuan Q, Luo Y, et al. (2025) Synthesis of Polysubstituted Benzo[][1,5]naphthyridine via Mn(III)-Mediated Domino Cascade Reactions of Cyclopropanols and 2-(2-Isocyanophenyl)acetonitriles. Organic Letters |
Qiu W, Tao R, He Y, et al. (2024) Enantioselective construction of C-B axially chiral alkenylborons by nickel-catalyzed radical relayed reductive coupling. Nature Communications. 15: 10432 |
Lin G, Guo Y, Zhang M, et al. (2024) Photogeneration of β-Borylsilyl Radical via Decarboxylation of -Hydroxyphthalimide Esters. Organic Letters |
Ma X, An Y, Li L, et al. (2024) Interception of Alkynyl Tetracoordinate Borons with Sulfur Electrophiles beyond the Zweifel Pathway. Angewandte Chemie (International Ed. in English). e202416579 |
Yang Y, Chen M, Xuan Q, et al. (2024) Rh(III)-Catalyzed Regioselective Alkyne Insertion in the Context of C-H Activation and Lactonization Reactions: Synthesis of Fused 1,2-Oxaphospholenes. Organic Letters |
Guo Y, Lin G, Zhang M, et al. (2024) Photo-induced decarboxylative C-S bond formation to access sterically hindered unsymmetric S-alkyl thiosulfonates and SS-alkyl thiosulfonates. Nature Communications. 15: 7313 |
Chen S, Wang YN, Xie J, et al. (2024) Chemo-, regio- and stereoselective access to polysubstituted 1,3-dienes via Nickel-catalyzed four-component reactions. Nature Communications. 15: 5479 |