【学术论文】
1. Ai Long, Di Li, Bo Yan, Yue Yuan, Haoqi Liu, Lan Yang, Yang Chen*, Shuzhong He* General one-step access to unsymmetric propargylic acetals via alcohol functionalization with allenyl ethers RSC Adv.2025, 15, 11770–11773.
2. Tao Long; Shuzhong He*; Chao Li* Research progress on the radical-polar crossover reaction in total synthesis of natural products. Chin. J. Org. Chem.2025, 45, 748–763.
3. Yanyan Que, Wenli Lei, Yin Fang, Shuzhong He*, Yang Chen* Recent advances in (4 + 3) cycloaddition of allenes. Green Synth. Catal., 2024, 5(4), 270–276.
4. Wenli Lei, Yuyang Song, Ai Long, Yanyan Que, Shuzhong He*; Hang Zhong*; Yang Chen* Stereoselective (4 + 3) cycloadditions of allenyl ethers-furans by chiral auxiliaries inducing and evaluation of anti-breast cancer activity. Front. Plant Sci.2022,12, 1087899–1087909.
5. Gang Yang, Xiangyu Feng, Congcong Han, Yang Chen, Shuzhong He* Synthesis of the ABC Ring System of Wallichanol Natural Product. Chin. J. Org. Chem.2021, 41, 726–730.
6. Xuefeng Liang, Weijian Ye, Waygen Thor, Lantian Sun, Bo Wang, Shuzhong He*, Yuen-Kit Cheng*, Chi-Sing Lee*, Construction of cyclopenta[b]pyran-2-ones viachemoselective (3 + 2) cycloaddition between 2-pyrones and vinyl cyclopropanes. Org. Chem. Front., 2020,7, 840–845.
7. Xian Huang, Waygen Thor, Xiangyu Feng, Liangliang Kang, Min Yang, Chi-Sing Lee*, Yuen-Kit Cheng*, Shuzhong He* (4 + 3) Cycloadditions of Allenyl Ether-Derived Oxygen-Stabilized Oxyallyls with Furans. Org. Chem. Front., 2020,7, 255–260.
8. Congcong Han, Yang Chen, Yin-Cheung Ching, Chi-Sing Lee, Shuzhong He* An approach towards the construction of the tetracyclic skeleton of palhinine alkaloids. Org. Chem. Front., 2020,7, 2243–2246.
9. Shuzhong He,Wei Yang, Lizhi Zhu, Guangyan Du, Chi-Sing Lee* Bioinspired total synthesis of (±)-yezo’otogirin C, Org. Lett.2014, 16(2), 496–499.
10. Shuzhong He, Richard P. Hsung,* William R. Presser, Zhi-Xiong Ma, and Bryan J. HaugenAn approach to cyclohepta[b]indoles through an allenamide (4 + 3) cycloaddition–Grignard cyclization–Chugaev elimination sequence, Org. Lett. 2014, 16, 2180–2183.