At NWU

22) X. Xin, J. Geng, D. Zhang, H. T. Ang, H. Wang, Y. Cheng, Y. Liu, R. W. Toh, J. Wu* and H. Wang.* Mechano-photoexcitation for organic synthesis using mechanoluminescent materials as photon sources. Nat. Synth. 2024, https://doi.org/10.1038/s44160-024-00681-8

21) L. Li, D. Wang, Y. Zhang, J. Liu, H. Wang,* and X. Luan.*  Diversification of Naphthol Skeletons Triggered by Aminative Dearomatization. Org. Lett. 2024, 26, 4910−4915.

20) S. Dong, C. Fu, Y. Ge, J. Liu,* H. Wang,* X. Luan.* Dearomatization/Spiroannulation of Halophenols Enables the Forging of Contiguous Quaternary Carbon Cyclohexadienones. Org. Lett. 2023, 25, 7841–7846.

19) L. Han, T. Liu, H. Wang,* X. Luan.* Palladium-Catalyzed Alkenyl C–H Activation/Diamination toward Tetrahydrocarbazole and Analogs Using Hydroxylamines as Single-Nitrogen Sources. Org. Lett. 2023, 25, 58–63.

18) W. Gao, H. Wang, Y. Liu, Qin Tang , Peng Wu, Tingting Lin, Tong Li,* Di Sun*. Sodium alginate-hydrogel coatings on extracorporeal membrane oxygenation for anticoagulation. Frontiers in Cardiovascular Medicine 2022, 9, 966649.

17) D. Sun,† H. Wang,† J. Liu,† X. Wang, H. Guo, L. Xue, L. Li, J. Li, B. Zhang, Y. Xue, S. Li, Y. Liu.* An enzyme cross-linked hydrogel as a minimally invasive arterial tissue sealing and anti-adhesion barrier. Nano Today 2022, 44, 101467.

16) N. Zhang,† Y. Ye,† L. Bai, J. Liu, H. Wang,* X. Luan.* Transition metal-free dearomatization of halonaphthols with C(sp3)-electrophiles. Chinese Chemical Letters 2021, 10.1016/j.cclet.2021.10.037

Prior to NWU

15) J. Xu, J. Cao, X. Wu, H. Wang, X. Yang, X. Tang, R. W. Toh, R. Zhou,* E. K. L. Yeow, J. Wu.* Unveiling extreme photoreduction potentials of donor−acceptor cyanoarenes to access aryl radicals from aryl chlorides. J. Am. Chem. Soc. 2021, 143, 33, 13266.

14) H. Wang,† H. Liu,† M. Wang,† M. Huang, X. Shi, T. Wang, X. Cong, J. Yan, J. Wu.* Bromine radical as a visible-light-mediated polarity-reversal catalyst. iScience 2021, 24, 102693.

13) C. Wang,† H.Wang,† C. Bolm.* Sulfoximines with α-ketoester functionalities at nitrogen from cyanoacetates and air. Adv.Synth. Catal. 2021, 363,747.

12) H. Wang,† R. W. Toh,† X. Shi, T. Wang, X. Cong, J. Wu.* Photo-mediated selective deconstructive geminal dihalogenation of trisubstituted alkenes. Nat Commun. 2020, 11, 4462. 

11) H. Wang, D. Zhang, M. Cao, C. Bolm.* Electrophilic sulfoximidations of thiols by hypervalent iodine reagents. Synthesis 2019, 51, 271. 

10) H. Wang, D. Zhang, C. Bolm.* Sulfoximidations of benzylic C-H bonds by photocatalysis. Angew. Chem. Int. Ed. 2018, 57, 5863. 

9) H. Wang, D. Zhang, C. Bolm.* Photocatalytic additions of 1-sulfoximidoyl-1,2-benziodoxoles to styrenes. Chem. Eur. J. 2018, 24, 14942. 

8) D. Zhang, H. Wang, C. Bolm.* Photocatalytic difunctionalisations of alkenes with N-SCN sulfoximines. Chem. Commun. 2018, 54, 5772. 

7) D. Zhang, H. Wang, H. Cheng, J. G. Hernández, C. Bolm.* An iodine-mediated hofmann-löffler-freytag reaction of sulfoximines leading to dihydroisothiazole oxides. Adv. Synth. Catal. 2017, 359, 4274. 

6) H. Wang, D. Zhang, H. Sheng, C. Bolm.* Sulfoximidoyl-containing hypervalent iodine(III) reagents: 1-sulfoximidoyl-1,2-benziodoxoles. J. Org. Chem. 2017, 82, 11854. 

5) H. Wang, Y. Cheng, P. Becker, G. Raabe, C. Bolm.* Synthesis of sulfoximidoyl-containing hypervalent  iodine(III) reagents and their use in transition-metal-free sulfoximidations of  alkynes. Angew. Chem. Int. Ed. 2016, 55, 12655. Highlighted by Synfacts (2016, 12, 1030). 

4) H. Wang, M. Frings, C. Bolm.* Halocyclizations of unsaturated sulfoximines. Org. Lett. 2016, 18, 2431. 

3) Y. Cheng, W. Dong, H. Wang, C. Bolm.* Rhodium-catalyzed ortho-amidations in the preparation of thiadiazine 1-oxides. Chem. Eur. J. 2016, 22, 10821.

2) H. Wang, Y. Xia, S. Lv, J. Xu, Z. Sun.* Facial and practical synthesis of benzimidazole-based N-heterocyclic carbenes. Tetrahedron Lett. 2013, 54, 2124.

1) K. Wen,† H. Wang,† J. Chen, H. Zhang, X. Cui, C. Wei, E. Fan, Z. Sun.* Improving carbene-copper-catalyzed  asymmetric  synthesis  of  α-aminoboronic  esters  using benzimidazole-based precursors. J. Org. Chem. 2013, 78, 3405.