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2025
151. Liu, Y., Wang J., Yin, Y.,* and Jiang, Z.,Recent Advances in Catalytic Atroposelective Synthesis of Axially Chiral Quinazolinones   Catalysts  2025,  DOI: 10.3390/catal1505042.
https://doi.org/10.3390/catal15050426
 

150. Dong, T.,Pan, Y.,# Zhao, X., Yin, Y., and Jiang, Z.,* Chiral Lewis Acid-Catalyzed Intramolecular [2 + 2] Photocycloaddition: Enantioselective Synthesis of Azaarene Functionalized Azabicyclo[2.1.1]hexanes and Bicyclo[1.1.1]pentanes  J. Am. Chem. Soc.   2025,  DOI: 10.1021/jacs.5c03542.
https://doi.org/10.1021/jacs.5c03542

149. Shao, T., Nie, F.,Cao, S., Li, Q.,  Zhao, X., Yin, Y., and Jiang, Z.,Kinetic Resolution of Racemic Radicals in Asymmetric Photoredox Minisci Reactions with Azaarenes for Precise Construction of Two Non-adjacent StereocentersJ. Am. Chem. Soc.   2025,  DOI: 10.1021/jacs.5c01623.
http://doi.org/10.1021/jacs.5c01623


148. Zhang, J.,‡ Guo, J., Xu, R., Zheng, D., Lian, K., Zhang, Z., Cao, S.,* and Jiang, Z., *  Catalytic asymmetric photocycloaddition reactions mediated by enantioselective radical approachesChem. Sci.  2025,  DOI: 10.1039/D5SC00358J.

147. Yin, Y., You, M., Li, X., Jiang, Z.*  Catalytic asymmetric photocycloaddition reactions mediated by enantioselective radical approachesChem. Soc. Rev.   2025,  DOI: 10.1039/d5cs00019j.

146. Sun, X., Zhu, W.Yin, Y., Zhao, X., Jiang, Z.*  From Radical Coupling to Enantioselective Controlled Protonation: Advancing Precise Construction of Stereocenters.   J. Am. Chem. Soc.   2025DOI: 10.1021/jacs.4c15276.

 



145. Jiang,C.,†  Meng, Y.,† Huang, Y., Liu, C., Yin, Y., Zhao, X., Cao, S.*Jiang, Z.* Chiral Primary Amine-Catalyzed Asymmetric Photochemical Reactions of Pyridotriazoles with Boronic Acids to Access Triarylmethanes.  J. Am. Chem. Soc.  2025DOI: 10.1021/jacs.4c16811.
http://doi.org/10.1021/jacs.4c16811

 

144. Li, Q., Zhao, X.,Yin, Y., Shao, T.,  Jiang, Z.*   Asymmetric Photoredox Catalytic Minisci-Type Reactions of αBromide AmidesOrg. Lett.  2025, DOI: 10.1021/acs.orglett.4c04791. 

 


​2024
 
143. Guo, Y.-Y.*, Tian, Z.-H., Zhang, L., Han, Y.-C., Zhang, B.-B., Xing, Q., Shao, T., Liu, Y., Jiang, Z.*J. Am. Chem. Soc.  2024DOI: 10.1021/jacs.4c10441
http://pubs.acs.org/doi/epdf/10.1021/jacs.4c10441


​142. Li, F., Liu, F.-Y., Zhao, X*, Yin, Y., Yu, B., Zhang, J.*, Jiang, Z.* Unified Enantioselective Allylations and Vinylogous Reactions Enabled by Visible Light-Driven Chiral Lewis Acid Catalysis. ACS Catal. 2024, 14, 16479−16487. DOI: 10.1021/acscatal.4c04638. 
https://pubs.acs.org/doi/10.1021/acscatal.4c04638
 


141. JiangC., Yin, Y.*, Jiang, Z.* Advances in Photoenzyme-Catalyzed Asymmetric Radical Addition Reactions. Chin. J. Org. Chem. 2024, DOI: 10.6023/cjoc202408004.
https://sioc-journal.cn/Jwk_yjhx/CN/10.6023/cjoc202408004

 


140. Wang, J., Fu, Q., Cao, S., Lv, X., Yin, Y., Ban, X., Zhao, X., Jiang, Z.* Enantioselective [2 + 2]  Photocycloreversion Enables De Novo Deracemization Synthesis of Cyclobutanes. J. Am. Chem. Soc.  2024146, 22840−22849. DOI: 10.1021/jacs.4c08290.
https://pubs.acs.org/doi/10.1021/jacs.4c08290
 

 

 
139. Liu, Y., Chu, M., Li, X., Cao, Z., Zhao, X., Yin, Y.*, Jiang, Z.* Photoredox Catalytic Deracemization Enabled Enantioselective and Modular Access to Axially Chiral N-Arylquinazolinones. Angew. Chem. Int. Ed. 2024, DOI: 10.1002/anie.202411236.
https://onlinelibrary.wiley.com/doi/10.1002/anie.202411236
 

 

 
138. Tian, D., Shi, W., Sun, X., Zhao, X.Yin, Y., Jiang, Z.*, Catalytic asymmetric [4+2] dearomative photocycloadditions of anthracene and its derivatives with alkenylazaarenes. Nat. Commun. 2024, 15 (1), 4563.
https://doi.org/10.1038/s41467-024-48982-y
 

 
 

 
137. Sun, X., Liu, Y., Yin, Y., Ban, X., Zhao, X.Jiang, Z.*, Asymmetric Photoredox Catalytic Formal De Mayo Reaction Enabled by Sensitization-Initiated Electron transferNat. Chem. 2024, 16, 1169-1176.
https://www.nature.com/articles/s41557-024-01502-3

 
 

 
136. Kong, M., Wang, Z., Ban, X., Zhao, X., Yin, Y., Zhang, J., Jiang, Z.*, Radical Cross Coupling and Enantioselective Protonation through Asymmetric Photoredox CatalysisAdv. Sci. 2024, 11 (12), 2307773 
https://doi.org/10.1002/advs.202307773
 

 

 
135. Fu, Q., Cao, S., Wang, J.*, Lv, X.*, Wang, H., Zhao, X.Jiang, Z.*, Enantioselective [2π + 2σ] Cycloadditions of Bicyclo[1.1.0]butanes with Vinylazaarenes through Asymmetric Photoredox CatalysisJ. Am. Chem. Soc. 2024, 146 (12), 8372-8380.
https://doi.org/10.1021/jacs.3c14077
 

 
 


 
134. Wei, W., Li, C., Fan, Y., Chen, X., Zhao, X., Qiao, B.*, Jiang, Z.*, Catalytic Asymmetric Redox-Neutral [3 + 2] Photocycloadditions of Cyclopropyl Ketones with Vinylazaarenes Enabled by Consecutive Photoinduced Electron TransferAngew. Chem. Int. Ed. 2024, e202406845.
https://doi.org/10.1002/anie.202406845
 


 


 
133. Zhang, L., You, M., Ban, X., Zhao, X., Yin, Y., Cao, S.*Jiang, Z.*, Visible Light-Driven Dearomative Ring Expansion of (Aza)arenes to Access Dihydrofuran-based Polycyclic Compounds. Chem. Sci.  2024, 15, 8828-8834.
https://doi.org/10.1039/D4SC00748D
 

 



132Ban, X.*, Jiang, Z.*, Asymmetric Photochemical Transformations Using a Chiral Hydrogen Bond DonorReference Module in Chemistry, Molecular Sciences and Chemical Engineering. 2024, DOI:org/10.1016/B978-0-32-390644-9.00135-9
https://doi.org/10.1016/B978-0-32-390644-9.00135-9

 


 
131. Wang, E.-M., Wang, Z., Ban, X., Zhao, X., Yin, Y.*Jiang, Z.*, Chemoselective Photocatalytic Sulfenylamination of Alkenes with Sulfenamides via Energy TransferChin. Chem. Lett. 2024, DOI:org/10.1016/j.cclet.2024.109843
https://doi.org/10.1016/j.cclet.2024.109843
 

 
 


 
130. Zhang, L., Ma, J., Ban, X., Zhao, X., Yin, Y., Jiang, Z.*, Direct Enantioselective Reduction of C=C Bond of β-Polyfluoro-alkylated Enones via Asymmetric Photoredox CatalysisSci China Chem. 2024, 67, 2016-2021.
http://doi.org/10.1007/s11426-023-1896-5
 
 


 
129. Jiang, Y., Yin, Y.*, Jiang, Z.* Recent Advances in Strategies for Halide Atom Transfer (XAT) and their ApplicationsChinese J. Org. Chem. 2024, 44, 1733-1759.
 

 
 
 


2023
 
 
128. Ma, C., Shen, J., Qu, C., Shao, T.*, Cao, S.*, Yin, Y., Zhao, X., Jiang, Z.*, Enantioselective Chemodivergent Three-Component Radical Tandem Reactions through Asymmetric Photoredox Catalysis. J. Am. Chem. Soc. 2023, 145 (36) 20141-20148.  
https://doi.org/10.1021/jacs.3c08883

 

 
127. Liu, Y., Zhang, L., Zhang, Y., Cao, S., Ban, X., Yin, Y., Zhao, X., Jiang, Z.*, Asymmetric Olefin Isomerization via Photoredox Catalytic Hydrogen Atom Transfer and Enantioselective Protonation. J. Am. Chem. Soc. 2023, 145 (33), 18307-18315.

 
126. Wang, B., Liu, Y., Jiang, C., Cao, Z., Cao, S., Zhao, X., Ban, X.*, Yin, Y.*, Jiang, Z.* Catalytic Asymmetric Hydrophosphinylation of 2-Vinylazaarenes to Access P-Chiral 2-Azaaryl-Ethylphosphine Oxides. Angew. Chem. Int. Ed. 2023, e202216605.

125. Wang, G., Li, L., Jiang, Y., Zhao, X., Ban, X. , Shao, T., Yin, Y. , Jiang, Z.* Kinetic Resolution of Azaarylethynyl Tertiary Alcohols by Chiral Bronsted Acid Catalysed Phosphine-Mediated Deoxygenation. Angew. Chem. Int. Ed. 2023, 62, e202214838.

124. Guo, Y.-Y., Tian, Z.-H., Ma, C., Han, Y.-C., Bai, D., Jiang, Z., Unlocking Mild-condition Benzene Ring Contraction Using Nonheme Diiron N-oxygenaseChem. Sci. 2023, 14 (42) 11907-11913.  
DOI
 

123. Yao, S., Zhao, X., Ban, X., Shao, T., Yin, Y., Hu, W.*, Jiang, Z.* Visible light-driven direct access to imine-containing azaarene-substituted highly functionalized pyrroles. Org. Chem. Front. 2023, 10 (19), 4779-4785. 
https://doi.org/10.1039/d3qo01056b.
 

 
122. Luo, C., Yin, Y., Jiang, Z.* Recent Advances in Asymmetric Synthesis of P-Chiral Phosphine Oxides. Chinese J. Org. Chem. 2023, 43 (6), 1963-1976.
https://doi.org/10.6023/cjoc202212024

 
121. Yin. Y., Jiang, Z.* Copper(I)-Catalyzed Asymmetric Conjugate Addition of 1,4-Dienes to β-Substituted Alkenyl Azaarenes. Chinese J. Org. Chem. 2023, 43 (3), 1203-1205.
https://doi.org/10.6023/cjoc202300014

 
120. Song, X., Zhang, Y., Li, Y., Zhao, X., Yin, Y., Ban, X., Jiang, Z.* Catalytic Asymmetric Synthesis of Azaarene-Functionalized Tertiary Amines and α-Amino Acid Derivatives from E/Z-Ketimine Mixtures via Enantioselective Radical Coupling. ACS Catal. 2023, 13 (9), 6396-6402.
https://doi.org/10.1021/acscatal.3c00756

 
119. Lv, X., Qi, Y.-N., Wang, J., Zhao, X., Jiang, Z.* Photoinduced Vinylogous Dearomatization. Org. Lett. 2023, 25 (17), 3114-3119.
https://doi.org/10.1021/acs.orglett.3c00966

 
118. Wang, J., Lv, X., Jiang, Z.* Visible-Light-Mediated Photocatalytic Deracemization. Chem. Eur. J. 2023, 29 (29), e202204029.
https://doi.org/10.1002/chem.202204029

 
117. Lv, X.*, Gao, P., Zhao, X., Jiang, Z.* Metal-Free Construction of Multisubstituted Indolizines via Intramolecular Amination of Allylic Alcohols. J. Org. Chem. 2023, 88 (13), 9459-9468.
https://doi.org/10.1021/acs.joc.3c00469

 
116. Guo, Y.-Y. *, Tian, Z.-H., Han, Y.-C., Ma, D., Shao, T., Jiang, Z.*, Hantzsch Ester as Efficient and Economical NAD(P)H Mimic for In Vitro Bioredox Reactions. Chem. Eur. J. 2023, 29 (45), e202301180.
https://doi.org/10.1002/chem.202301180

 
115. Shao, T.*, Ban, X., Jiang, Z.* α-Amino Acids: An Emerging Versatile Synthon in Visible Light-Driven Decarboxylative Transformations. Chem. Rec. 2023, e202300122.
https://doi.org/10.1002/tcr.202300122

 

114. Dai, Y., Huang, H., Liang, S., Yin, Y., Ban, X., Zhao, X., Jiang, Z.* Catalytic Asymmetric Intermolecular [3 + 2] Photocycloaddition of Cyclopropylamines with Electron-Deficient Olefins. Org. Lett. 2023, 25 (24), 4551-4555.
https://doi.org/10.1021/acs.orglett.3c01585