35. Zhao, C.;† Gao, R.;† Ma, W.; Li, M.; Li, Y.; Zhang, Q.; Guan, W.;* Fu, J.-K.*
A Facile Synthesis of α,β-Unsaturated Imines via Palladium-Catalyzed Dehydrogenation
Nat. Commun. 2024, 15, 4329.
https://www.nature.com/articles/s41467-024-48737-9
34. Dong, J.;† Liang, Y.;† Li, Y.;† Guan, W.;* Zhang, Q.; Fu, J.-K.*
A Catalytic Three-Component Aminofluorination of Unactivated Alkenes with Electron-Rich Amino Sources
Adv. Sci. 2024, 11, 2305006.
https://onlinelibrary.wiley.com/doi/10.1002/advs.202305006
33. Wang, T.;†,* Yu, W.;† Lan, J.;† Wang, H.; Jiang, Z.; Li, Y.; Fu, J.-K.*
Visible-Light-Driven Three-Component Reductive 1,2-Diarylation of Alkenes
Chem Catal. 2023, 3, 100619.
https://www.sciencedirect.com/science/article/pii/S2667109323001343
32. Li, Y.;† Dong, Y.;† Wang, X.;† Li, G.; Xue, H.; Xin, W.; Zhang, Q.; Guan, W.*; Fu, J.-K.*
Regio-, Site- and Stereoselective Three-Component Aminofluorination of 1,3-Dienes via Cooperative Silver Salt and Copper Catalysis
ACS Catal. 2023, 13, 2410-2421.
https://pubs.acs.org/doi/full/10.1021/acscatal.2c06025
31. Zhao, C.;† Li, Y.;† Dong, Y.;† Li, M.; Xia, D.; Gao, S.; Zhang, Q.; Liu, Q.; Guan, W.*; Fu, J.-K.*
Divergent Regioselective Heck-type Reaction of Unactivated Alkenes and N-Fluoro-sulfonamides
Nat. Commun. 2022, 13, 6297.
https://www.nature.com/articles/s41467-022-33996-1
30. Zhao, C.; Zhu, D.-S.*; Fu, J.-K.*
Alkene difunctionalization via aminyl radicals
Trends in Chemistry 2022, doi: org/10.1016/j.trechm.2022.08.003. (Invited Review, MOM).
https://www.sciencedirect.com/science/article/abs/pii/S2589597422001952?via%3Dihub
29. Huo, L.-Q.; Shi, L.-L.*; Fu, J.-K.*
Iron-Copper Dual Catalysis Enabling C−C and C−X (X = N, B, P, S, Sn) Bond Formation
Eur. J. Org. Chem. 2022, e202200454. (Invited Review).
https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/ejoc.202200454
28. Yang, L.;† Huang, Y.;† Yu, W.; Fan, L.; Wang, T.*; Fu, J.-K.*
Copper-Catalyzed Oxidative Coupling of Quinazoline-3-Oxides: Synthesis of O-Quinazolinic Carbamates
J. Org. Chem. 2022, 87, 5136-5148.
https://pubs.acs.org/doi/10.1021/acs.joc.1c03098
27. Li, Y.;† Bao, J.;† Zhang, Y.; Peng, X.; Yu, W.; Wang, T.; Yang, D.; Liu, Q.; Zhang, Q.; Fu, J.-K.*
Three-Component Aminofluorination of Alkenes with Electronically Rich Amino Sources
Chem 2022, 8, 1147-1163.
https://www.sciencedirect.com/science/article/pii/S2451929422000997
26. Wang, X.; Li, D.; Zhang, J.-L.; Gong, J.-X.; Fu, J.-K.*, Yang, Z.*
A Synthetic Route to The Core Structure of (−)-Retigeranic Acid A
Org. Lett. 2021, 23, 5092-5097.
https://pubs.acs.org/doi/10.1021/acs.orglett.1c01633
25. Li, Y.;† Ali, A.;† Dong, J.; Zhang, Y.; Shi, L.-L.; Liu, Q.; Fu, J.-K.*
Copper-Catalyzed Diamination of Unactivated Alkenes With Electron-Rich Amino Sources
Org. Lett. 2021, 23, 4072-4077. (†equal contribution)
https://pubs.acs.org/doi/10.1021/acs.orglett.1c01313
24. Liu, S.-Z.;† Yang, L.-Y.;† Tao, J.-S.; Yu, W.-J.; Wang, T.*; Fu, J.-K.*
Nickel-Catalyzed Oxidative Transamidation of Tertiary Aromatic Amines with N-Acylsaccharins
Synlett, 2021, DOI: 10.1055/a-1517-5895. (invited article as part of the Cluster "Modern Nickel-Catalyzed Reactions")
"Featured in Org. Chem. Highlights" (https://www.organic-chemistry.org/Highlights/2022/27June.shtm)
https://www.thieme-connect.de/products/ejournals/abstract/10.1055/a-1517-5895
23. Gao, S.-Q.; Shi, L.-L.*; Chang, L.; Wang, B.-L.; Fu, J.-K.*
Recent Developments in Heck-Type Reaction of Unactivated Alkenes and Alkyl Electrophiles
Synthesis, 2021, 53, 861–878. (invited short review)
https://www.thieme-connect.de/products/ejournals/abstract/10.1055/s-0040-1705966
22. Zhang, Z.-C.;† Zhao, D.-D.;† Zhang, Z.-C.; Tan, X.-Y.; Gong, J.-X.*; Fu, J.-K.*; Yang, Z.*
Synthesis of 4-Desmethyl-rippertenol and 7-Epi-rippertenol via Photo-induced Cyclization of Dienones
CCS Chemistry, 2020, 2, 2074-2083. (†equal contribution)
https://www.chinesechemsoc.org/doi/10.31635/ccschem.020.202000398
21. Deng, Y.;† Zhao, C.;† Zhou, Y.;† Wang, H.; Li, X.; Cheng, G.-J.; Fu, J.-K.*
Directing-Group-Based Strategy Enabling Intermolecular Heck-Type Reaction of Cycloketone Oxime Esters and Unactivated Alkenes
Org. Lett. 2020, 22, 3524-3530. (†equal contribution)
https://pubs.acs.org/doi/10.1021/acs.orglett.0c00963
20. Li, Y.;† Liang, Y.-J.;† Dong, J.-C.; Deng, Y.; Zhao, C.-Y.; Su, Z.-M.; Guan, W.*; Bi, X.-H.*; Liu, Q.; Fu, J.-K.* (Cover, †equal contribution)
Directed Copper-Catalyzed Intermolecular Aminative Difunctionalization of Unactivated Alkenes
J. Am. Chem. Soc. 2019, 141, 18475-18485. (†equal contribution)
东北师范大学主页报道：http://www.nenu.edu.cn/info/1055/11203.htm
“化学加”微信公众号推送：https://mp.weixin.qq.com/s/NkCyc3NAXh5JBH8xZPWQyQ
“研之成理”微信公众号推送：https://mp.weixin.qq.com/s/PBHMGzQdeDEjmJmdCVWm2g
https://pubs.acs.org/doi/10.1021/jacs.9b07607
19. Yu, W.-J.; Chen, L.; Tao, J.-S.; Wang, T.*; Fu, J.-K.*
Dual Nickel- and Photoredox-Catalyzed Reductive Cross-coupling of Aryl Vinyl Halides and Unactivated Tertiary Alkyl Bromides
Chem. Commun. 2019, 55, 5918-5921.
https://pubs.rsc.org/en/content/articlelanding/2019/CC/C9CC00768G#!divAbstract
18. Tian, L.; Gao, S.-Q.; Wang, R.; Li, Y.; Tang, C.-L.; Shi, L.-L.*; Fu, J.-K.*
Copper-catalyzed Ring-opening C(sp3)-N Coupling of Cycloketone Oxime Esters: Access to 1º, 2º and 3º Alkyl Amines
Chem. Commun. 2019, 55, 5347-5350.
https://pubs.rsc.org/en/content/articlelanding/2019/CC/C9CC02030F#!divAbstract
17. Tang, C.-L.;† Zhang, R.;† Zhu, B.;† Fu, J.-K.*; Deng, Y.; Tian, L.; Guan, W.*; Bi, X.-H.* (Cover, †equal contribution)
Directed Copper-Catalyzed Intermolecular Heck-Type Reaction of Unactivated Olefins and Alkyl Halides
J. Am. Chem. Soc. 2018, 140, 16929-16935.
东北师范大学主页报道：http://www.nenu.edu.cn/2018/1122/c139a33334/page.htm
CBG资讯报道：https://www.chembeango.com/zixun/32859
https://pubs.acs.org/doi/10.1021/jacs.8b10874
16. Yu, W.-J.; Yang, S.-W.; Xiong, F.; Fan, T.-X.; Feng, Y.; Huang, Y.-Y.; Fu, J.-K.*; Wang, T.*
Palladium-catalyzed carbonylation of benzylic ammonium salts to amides and esters via C–N bond activation
Org. Biomol. Chem. 2018, 16, 3099-3103.
https://pubs.rsc.org/en/content/articlelanding/2018/OB/C8OB00488A#!divAbstract
15. Li, Y.; Zhang, R.; Bi, X.-H.*; Fu, J.-K.*
Multifunctionalization of Unactivated Cyclic Ketones via Synergistic Catalysis of Copper and Diarylamine: Access to Cyclic α‑Enaminone
Org. Lett. 2018, 20, 1207-1211.
https://pubs.acs.org/doi/10.1021/acs.orglett.8b00125
14. Fu, J.-K.; Zanoni, G.; Anderson, E. A.; Bi, X.-H.*
α-Substituted vinyl azides: an emerging functionalized alkene
Chem. Soc. Rev. 2017, 46, 7208-7228.
https://pubs.rsc.org/en/content/articlelanding/2017/CS/C7CS00017K#!divAbstract
13. Zhang, R.; Li, Y.; Ali, A.; Hao, J.-M.; Bi, X.-H.*; Fu, J.-K.*
Rh(II)-Catalyzed Tandem Cyclization of Aliphatic N-Sulfonyl-1,2,3-triazoles and Alcohols for the Synthesis of 6-Alkoxy Piperidin-3-ones
Adv. Synth. Catal. 2017, 359, 4057-4061.
https://onlinelibrary.wiley.com/doi/full/10.1002/adsc.201700882
12. Gu, Y.-Q.; Yuan, H.; Fu, J.-K.*; Gong, J.-X.*; Yang, Z.*
Asymmetric Formal Synthesis of Cortistatins via a Gold-Catalyzed Semi-Pinacol Rearrangement Strategy
Acta Chim. Sinica 2017, 75, 798-807. (Invited Article)
http://sioc-journal.cn/Jwk_hxxb/CN/10.6023/A17040190
11. Li, Y.; Zhang, R.; Ali, A.; Zhang, J.; Bi, X.-H.*; Fu, J.-K.*
Synthesis of 6-Substituted Piperidin-3-ones via Rh(II)-Catalyzed Transannulation of N-Sulfonyl-1,2,3-triazoles with Electron-Rich Aromatic Nucleophiles
Org. Lett. 2017, 19, 3087-3090.
https://pubs.acs.org/doi/10.1021/acs.orglett.7b01180
10. Fang, G.-C.; Liu, J.-Q.; Fu, J.-K.*; Liu, Q.; Bi, X.-H.*
Silver-Catalyzed Cascade Reaction of β-Enaminones and Isocyanoacetates To Construct Functionalized Pyrroles
Org. Lett. 2017, 19, 1346-1349.
https://pubs.acs.org/doi/10.1021/acs.orglett.7b00201
Before NENU:
9. Fu, J.-K.; Gu, Y.-Q.; Yuan, H.; Luo, T.-P.; Liu, S.; Lan, Y.*; Gong, J.-X.*; Yang, Z.*
Towards a general diastereoselective route to oxabicyclo[3.2.1]octanes via a gold-catalysed cascade reaction
Nat. Commun. 2015, 6, 8617.
https://www.nature.com/articles/ncomms9617
8. Fu, J.-K.; Shen, H.-J.; Chang, Y.-Y.; Li, C.-C.; Gong, J.-X.; Yang, Z.*
Concise Stereoselective Synthesis of Oxaspirocycles with 1-Tosyl-1,2,3-triazoles: Application to the Total Syntheses of (±)-Tuberostemospiroline and (±)-Stemona-lactam R
Chem. Eur. J. 2014, 20, 12881-12888. (Highlighted in Org. Chem., May, 11th, 2015)
https://onlinelibrary.wiley.com/doi/full/10.1002/chem.201403756
7. Fu, J.-K.; Shang, H.; Wang, Z.-F.; Chang, L.; Shao, W.-B.; Yang, Z.*; Tang, Y.-F.*
Gold-Catalyzed Rearrangement of Allylic Oxonium Ylides: Efficient Synthesis of Highly Functionalized Dihydrofuran-3-ones
Angew. Chem. Int. Ed. 2013, 52, 4198-4202.
https://onlinelibrary.wiley.com/doi/full/10.1002/anie.201208305
6. Southgate, E.;† Pospech, J.;† Fu, J.-K.; Holycross, D. R.; Sarlah, D.* (†equal contribution)
Dearomative Dihydroxylation with Arenophiles
Nat. Chem. 2016, 8, 922-928.
https://www.nature.com/articles/nchem.2594
5. Shen, H.-J.; Fu, J.-K.; Hao, Y.; Gong, J.-X.*; Yang, Z*.
Synthesis of 2,3-Disubstituted Indoles and Benzofurans by the Tandem Reaction of Rhodium(II)-Catalyzed Intramolecular C–H Insertion and Oxygen-Mediated Oxidation
J. Org. Chem. 2016, 81, 10180-10192.
https://pubs.acs.org/doi/10.1021/acs.joc.6b00611
4. Gu, Y.-Q.; Zhang, P.-P.; Fu, J.-K.; Liu, S.; Lan, Y.*; Gong, J.-X.*; Yang, Z.*
Regio- and Stereoselective Syntheses of 7-Oxabicyclo[2.2.1]heptanes via a Gold(I)-Catalyzed Cycloisomerization of Alkynediols: Asymmetric Total Synthesis of Farnesiferol C
Adv. Synth. Catal. 2016, 358, 1392-1397.
https://onlinelibrary.wiley.com/doi/full/10.1002/adsc.201600218
3. Shen, H.-J.; Fu, J.-K.; Gong, J.-X.*; Yang, Z.*
Tunable and Chemoselective Syntheses of Dihydroisobenzofurans and Indanones via Rhodium-Catalyzed Tandem Reactions of 2-Triazole-benzaldehydes and 2-Triazole-alkylaryl ketones
Org. Lett. 2014, 16, 5588-5591.
https://pubs.acs.org/doi/10.1021/ol502617m
2. Wang, Z.-F.; Zhao, K.; Fu, J.-K.; Zhang, J.-L.; Yin, W.-Y.; Tang, Y. F.*
Organocatalytic 1,4-Conjugate Addition of Ascorbic Acid to α,β-unsaturated Aldehydes: Bio-inspired Total Syntheses of Leucodrin, Leudrin and Proposed Structure of Dilaspirolactone
Org. Biomol. Chem. 2013, 11, 2093-2097.
https://pubs.rsc.org/en/content/articlelanding/2013/OB/c3ob00046j#!divAbstract
1. Chang, L.; Jiang, H.; Fu, J.-K.; Liu, B.; Li, C.-C.*; Yang, Z*.
Synthesizing the Tetracyclic Core of Nanolobatolide
J. Org. Chem. 2012, 77, 3609-3614.