Zhanhui Yang

l  2025

1.      Yujie Zhang, Kangjia Zhang, Jiaxi Xu, Zhanhui Yang*. Iridium-catalyzed N-methylation of drug molecules. Green Chem.2025, 27, 5136-5148. https://doi.org/10.1039/d4gc05652c

2.      Tingting Wang, Zhanhui Yang*. Sterically Directed Site‐ and Stereoselective O‐Glycosylation of tert‐Butyl Gentisate. Chem–Asian J.2025, 20, e00359. https://doi.org/10.1002/asia.202500359

3.      Cunzhi Chen, Hongguang Du*, Jiaxi Xu, Zhanhui Yang*. Origins of Regio- and Enantiocontrol in Rhodium-Catalyzed Synthesis of Alkylidene Dihydrothiophenes from 1,2,3-Thiadiazoles and Allenes. J. Org. Chem.2025, 90, 11124–11131. https://doi.org/10.1021/acs.joc.5c01021

4.      Cunzhi Chen, Youwei Chen, Hongguang Du, Jiaxi Xu, Zhanhui Yang*. Enantioselective and Regiodivergent Skeletal Transformations of 1,2,3-Thiadiazoles to Alkylidene Dihydrothiophenes. Org. Lett.2025, 27, 4337–4342. https://doi.org/10.1021/acs.orglett.5c01067

5.      Liu Li, Hao Wei, Zhanhui Yang, Jiaxi Xu*. Ce(OTf)3-Catalyzed Asymmetric 6π Cyclization of Triaryldivinyl Ketones.Org. Lett.2025, 27, 4875–4879. https://doi.org/10.1021/acs.orglett.5c01081

6.      Jingyu Zhang, Yang Chen, Jiaxi Xu, Zhanhui Yang*. Phthalimidine Synthesis via Iridium-Catalyzed Reductive Lactamization. J. Org. Chem.2025, 90, 691–699. https://doi.org/10.1021/acs.joc.4c02615

7.      Yujie Zhang^#, Asad Aziz^#, Jiaxi Xu, Zhanhui Yang*. Rare Earth Catalyzed Redox‐Neutral (4+1) Annulations Between Ortho‐Aminobenzenesulfonamides and Aldehydes. ChemistrySelect2025, 10, e03641. https://doi.org/10.1002/slct.202503641

8.      Zhanhui Yang, Cunzhi Chen. 4‐(1,1‐Dimethylethyl)‐1,2,3‐thiadiazole. In Encyclopedia of Reagents for Organic Synthesis,2025. https://doi.org/10.1002/047084289X.rn02601

l  2024

9.      Cunzhi Chen^#, Kang Lv^#, Youwei Chen, Hongguang Du, Jiaxi Xu, Tao Liu*, Zhanhui Yang*. Catalytic Enantioselective (3+2) Annulations of Nucleophilic Thioacyl Rh(I)-Carbenes with Achmatowicz Rearrangement Products. ACS Catal.2024, 14, 8949−8957.https://doi.org/10.1021/acscatal.4c02814

10.  Jiayan Li, Ziyang Dong, Yang Chen, Zhanhui Yang, Xinen Yan, Meng Wang, Chenyang Li*, Changgui Zhao*. N-Heterocyclic carbene-catalyzed enantioselective synthesis of planar-chiral cyclophanes via dynamic kinetic resolution. Nat Commun2024, 15, 2338. https://doi.org/10.1038/s41467-024-46376-8

11.  Yang Chen, Jingyu Zhang, Yecheng Wang, Hongguang Du, Jiaxi Xu, Zhanhui Yang*. En Route to Diastereopure Polycyclic γ-Lactones by Iridium-Catalyzed Hydride Transfer. Chin. J. Chem. 2024, 42, 3047-3055. https://doi.org/10.1002/cjoc.202400265

12.  Jun Dong, Zhanhui Yang*. Catalytic One‐Pot Reductive Amination of Carboxylic Acids. ChemCatChem2024, 16, e202301427.https://doi.org/10.1002/cctc.202301427

13.  Yang Chen, Jingyu Zhang, Hongguang Du,* Renshi Luo,* Jiaxi Xu, Zhanhui Yang*. Iridium-catalyzed reductive γ-lactonization of ortho-acylbenzoic acids in water: sustainable access to phthalides. Org. Chem. Front.2024, 11, 2220-2230. https://doi.org/10.1039/D3QO02019C

14.  Yujie Zhang, Shukui Shi, Zhanhui Yang*. Thiourea-Mediated Stereospecific Deoxygenation of Cyanoepoxides to Access Highly Diastereopure Alkenyl Nitriles. J. Org. Chem.2024, 89, 2748-2758. https://doi.org/10.1021/acs.joc.3c02869

15.  Hao Wei, Yujie Zhang, Sanlin Jin, Ying Yu*, Ning Chen, Jiaxi Xu, Zhanhui Yang*. PyBox–La(OTf)3-Catalyzed Enantioselective Diels–Alder Cycloadditions of 2-Alkenoylpyridines with Cyclopentadiene. Molecules2024, 29, 2978. https://doi.org/10.3390/molecules29132978

16.  Youwei Chen, Jide Li, Jiaxi Xu, Zhanhui Yang*. Iridium-Catalyzed Highly Selective 1,4-Reduction of α,β-Unsaturated Carbonyl Compounds. Molecules2024, 29, 5912. https://doi.org/10.3390/molecules29245912

17.  Chengzhuo Wang, Ning Chen, Zhanhui Yang, Jiaxi Xu*. Y(OTf)₃-Salazin-Catalyzed Asymmetric Aldol Condensation. Molecules2024, 29, 1963. https://doi.org/10.3390/molecules29091963

18.  Hao Wei, Cunzhi Chen, Aijun Gao*, Zhanhui Yang*. Rh(I)-catalyzed enantioselective (3 + 2) transannulations of 1,2,3-thiadiazoles with P-chiral monodentate phosphines. Phosphorus, Sulfur Silicon Relat. Elements2024, 199, 157-161.https://doi.org/10.1080/10426507.2023.2281473

l  2023

19.  Tingting Wang, Rui Miao, Renshi Luo, Jiaxi Xu, Zhanhui Yang*. Furan-2-yl Anions as γ-Oxo/Hydroxyl Acyl Anion Equivalents Enabled by Iridium-Catalyzed Chemoselective Reduction. Org. Lett.2023, 25, 4705-4710. https://doi.org/10.1021/acs.orglett.3c01634

20.  Lu Ouyang, Rui Miao, Zhanhui Yang*, Renshi Luo*. Iridium-catalyzed reductive amination of carboxylic acids. J. Catal.2023, 418, 283-289. https://doi.org/10.1016/j.jcat.2023.01.030

21.  Lu Ouyang, Yuqiu Liang, Sen Wang, Rui Miao, Jianhua Liao, Zhanhui Yang*, Renshi Luo*.  Iridium-catalyzed reductive hydroamination of terminal alkynes in water. J. Catal.2023, 427, 115096. https://doi.org/10.1016/j.jcat.2023.115096

22.  Cunzhi Chen, Shuyan Fang, Mingwu Yu, Jiaxi Xu, Zhanhui Yang*. Catalytic site-specific and regioselective (3 + 2) transannulations between 1,2,3-thiadiazoles and allenoates. Org. Chem. Front.2023, 10, 661-667. https://doi.org/10.1039/D2QO01662A

23.  Jing Wang, Tingting Wang, Hongguang Du, Ning Chen*, Jiaxi Xu, Zhanhui Yang*. Accessing para-Alkylphenols via Iridium-Catalyzed Site-Specific Deoxygenation of Alcohols. J. Org. Chem.2023, 88, 12572-12584. https://doi.org/10.1021/acs.joc.3c01294

24.  Yang Chen, Meng-Yao Ma, Hongguang Du*, Jiaxi Xu, Zhanhui Yang*. Late-Stage Two-Step C11–H Arylation of Dibenzooxa/thiazepines. Synthesis2023, 55, 2195-2205. https://doi.org/10.1055/a-2038-2323

l  2022

25.  Tingting Wang, Changmeng Liu, Dong Xu, Jiaxi Xu, Zhanhui Yang*. Iridium-Catalyzed and pH-Dependent Reductions of Nitroalkenes to Ketones. Molecules2022, 27, 7822. https://doi.org/10.3390/molecules27227822

26.  Changmeng Liu, Yang Chen, Zhanhui Yang*. Iridium-Catalyzed Stereoselective Transfer Hydrogenation of 1,5-Benzodiazepines. J. Org. Chem.2022, 87, 12001-12018. https://doi.org/10.1021/acs.joc.2c01006

27.  Ziyang Dong, Meng-Yao Ma, Jiaxi Xu, Zhanhui Yang*. Catalytic (3 + 2) umpolung annulations of α-thioacyl carbenes with aryl isothiocyanates. Chem. Commun.2022, 58, 7980-7983. https://doi.org/10.1039/D2CC02882D

28.  Zhanhui Yang*. Partial reductions of carboxylic acids and their derivatives to aldehydes. Org. Chem. Front.2022, 9, 3908-3931. https://doi.org/10.1039/D2QO00748G

29.  Cunzhi Chen, Shuyan Fang, Ziyang Dong, Jiaxi Xu, Zhanhui Yang* Catalytic Diastereospecific and Enantioselective (3+2) Transannulations of 1,2,3-Thiadiazoles with Strained Norbornene Derivatives. Org. Lett.2022, 24, 2110–2114. https://doi.org/10.1021/acs.orglett.2c00330

l  2021

30.  Ziyang Dong, Cunzhi Chen, Jing Wang, Jiaxi Xu, Zhanhui Yang*. Dual roles of bisphosphine and epoxy: Rh-catalyzed highly chemo- and diastereoselective (3 + 2) transannulations of 1,2,3-thiadiazoles with cyanoepoxides. Org. Chem. Front.2021, 8, 6687–6698. https://doi.org/10.1039/D1QO01220G

31.  Dong Xu, Yang Chen, Changmeng Liu, Jiaxi Xu, Zhanhui Yang*. Iridium-catalyzed highly chemoselective and efficient reduction of nitroalkenes to nitroalkanes in water. Green Chem.2021, 23, 6050-6058. https://doi.org/10.1039/D1GC01907D

32.  Tingting Wang, Yang Chen, Ning Chen, Jiaxi Xu, Zhanhui Yang*. Iridium-catalyzed highly stereoselective deoxygenation of tertiary cycloalkanols: stereoelectronic insights and synthetic applications.Org. Biomol. Chem. 2021, 19, 9004-9011. https://doi.org/10.1039/d1ob01690c

33.  Yang Chen, Tingting Wang, Hongguang Du*, Jiaxi Xu, Zhanhui Yang*. Proton-Mediated Practical Synthesis of McGeachin-Type Bisaminals. Synthesis 2021, 53, 2828-2840. https://doi.org/10.1055/a-1490-1241

34.  Qiuyue Wu, Ziyang Dong, Jiaxi Xu*, Zhanhui Yang*. Sulfur-controlled and rhodium-catalyzed formal (3 + 3) transannulation of thioacyl carbenes with alk-2-enals and mechanistic insights. Org. Biomol. Chem., 2021, 19, 3173-3180. https://doi.org/10.1039/d1ob00116g

l  2020

35.  Ziyang Dong, Zhanhui Yang*, Jiaxi Xu. Structural Modifications and Chiral Applications of Brucine.Chin. J. Org. Chem.2020, 40, 4101-4121 (in Chinese: 董子阳, 杨占会*, 许家喜. 马钱子碱的结构修饰和手性应用. 有机化学, 2020, 40, 4101-4121.)https://doi.org/10.6023/cjoc202004049

36.  Yang Chen^#, Siqi Li^#, Shili Hou, Jiaxi Xu*, Zhanhui Yang*. Chiral Synthesis of McGeachin-Type Bisaminals. J. Org. Chem. 2020, 85, 3709-3716. https://doi.org/10.1021/acs.joc.9b03362

37.  Dong Xu, Shiyi Yang, Aijun Gao*, Zhanhui Yang*. NaClO₂-mediated preparation of pyridine-2-sulfonyl chlorides and synthesis of chiral sulfonamides. J. SulfurChem.2020,41, 463-473. https://doi.org/10.1080/17415993.2020.1775834

l  2019

38.  Jide Li, Weiping Tang, Demin Ren, Jiaxi Xu*, Zhanhui Yang*. Iridium-catalysed highly selective reduction–elimination of steroidal 4-en-3-ones to 3,5-dienes in water. Green Chem.2019, 21, 2088-2094. https://doi.org/10.1039/C9GC00654K

39.  Bingnan Zhou, Qiuyue Wu, Ziyang Dong, Jiaxi Xu*, Zhanhui Yang*. Rhodium-Catalyzed 1,1-Hydroacylation of Thioacyl Carbenes with Alkynyl Aldehydes and Subsequent Cyclization. Org. Lett.2019, 21, 3594-3599. https://pubs.acs.org/doi/10.1021/acs.orglett.9b01003

40.  Yang Chen, Hongyi Qi, Ning Chen, Demin Ren, Jiaxi Xu*, Zhanhui Yang*. Fluorium-Initiated Dealkylative Cyanation of Thioethers to Thiocyanates. J. Org. Chem.2019, 84, 9044-9050. https://doi.org/10.1021/acs.joc.9b00965

41.  Ziyang Dong^#, Yang Chen^#, Zhiheng Yang, Zhanhui Yang*, Jiaxi Xu*. A Tandem Sulfonylation and Knoevenagel Condensation for the Preparation of Sulfocoumarin-3-carboxylates. Synthesis2019, 51, 1809-1818. https://doi.org/10.1055/s-0037-1611703

l  2018

42.  Shiyi Yang, Weiping Tang, Zhanhui Yang*, Jiaxi Xu*. Iridium-catalyzed highly efficient and site-selective deoxygenation of alcohols in water. ACS Catal.2018, 8, 9320–9326. https://pubs.acs.org/doi/10.1021/acscatal.8b02495

43.  Zhicheng Fu, Wenhao Yuan, Ning Chen, Zhanhui Yang*, Jiaxi Xu*. Na₂S₂O₈-mediated efficient synthesis of isothiocyanates from primary amines in water. Green Chem. 2018, 20, 4484–4491. https://doi.org/10.1039/C8GC02261E

44.  Ji-tian Liu^#, Shiyi Yang^#, Weiping Tang, Zhanhui Yang*, Jiaxi Xu*. Iridium-catalyzed efficient reduction of ketones in water with formic acid as a hydride donor at low catalyst loading. Green Chem.2018, 20, 2118-2124. https://doi.org/10.1039/C8GC00348C

45.  Wei He, Yong Ding, Jianzhuo Tu, Chuqiang Que, Zhanhui Yang* and Jiaxi Xu*. Thermal conversion of primary alcohols to disulfides via xanthate intermediates: an extension to Chugaev elimination.Org. Biomol. Chem.2018, 16, 1659-1666.https://doi.org/10.1039/c8ob00024g

46.  Wei Xu, Zhicheng Fu, Zhanhui Yang, Lidan Zhang, Jiaxi Xu*. Synthesis of 4-trifluoromethyl-β-sultams via sulfa-Staudinger cycloadditions. Phosphorus, Sulfur, Silicon Relat. Elem.2018, 193, 335-344. http://dx.doi.org/10.1080/10426507.2017.1418741

l  2017

47.  Wei He^#, Junpeng Zhuang^#, Hongguang Du, Zhanhui Yang* and Jiaxi Xu*. Stereochemistry and mechanistic insights in the [2^t + 2ⁱ + 2ⁱ] annulations of thioketenes and imines. Org. Biomol. Chem.2017, 15, 9424–9432. https://doi.org/10.1039/c7ob02212c

48.  Zhanhui Yang, Renshi Luo, Zhongpeng Zhu, Xuerong Yang and Weiping Tang*. Harnessing the Reactivity of Iridium Hydrides by Air: Iridium-Catalyzed Oxidation of Aldehydes to Acids in Water. Organometallics 2017,36, 4095–4098. https://doi.org/10.1021/acs.organomet.7b00634

49.  Zhanhui Yang^#, Zhongpeng Zhu^#, Renshi Luo, Xiang Qiu, Ji-tian Liu, Jing-Kui Yang and Weiping Tang*. Iridium-catalyzed Highly Efficient Chemoselective Reduction ofAldehydes in Water using Formic Acid as the Hydrogen Source.Green Chem.2017, 19, 3296-3301 (Z.Y. and Z.Z. contributed equally). https://doi.org/10.1039/C7GC01289F

50.  Wei He^#, Junpeng Zhuang^#, Zhanhui Yang*, Jiaxi Xu*. Sterically controlled diastereoselectivity in thio-Staudinger cycloadditions of alkyl/alkenyl/aryl- substituted thioketenes. Org. Biomol. Chem.2017, 15, 5541–5548. https://doi.org/10.1039/c7ob01214d

51.  Zhanhui Yang, Shiyi Yang, Jiaxi Xu*. Sulfur-directed metal-free and regiospecific methyl C(sp³)–H imidation of thioanisoles. Tetrahedron2017, 73, 3240–3248.https://doi.org/10.1016/j.tet.2017.04.054

52.  Zhanhui Yang, Shiyi Yang, Muhammad Sohail Haroone, Wei He, Jiaxi Xu*. Sulfur-mediated C(sp²)–H imidation and 1,2-imidofluorination of vinyl sulfides. Tetrahedron2017, 73, 3338–3346. https://doi.org/10.1016/j.tet.2017.04.057

53.  Zhanhui Yang, Hassane Abdellaoui, Wei He and Jiaxi Xu*. Ortho-Nitro Effect on the Diastereoselective Control in Sulfa-Staudinger and Staudinger Cycloadditions. Molecules2017, 22, 784. https://doi.org/10.3390/molecules22050784

54.  Peipei Huang, Zhanhui Yang*, Jiaxi Xu*. Specific intramolecular aromatic C–H insertion of diazosulfonamides. Tetrahedron2017, 73, 3255–3265.https://doi.org/10.1016/j.tet.2017.04.056

55.  Jing Liu, Jianzhuo Tu, Zhanhui Yang, Chol-Ung Pak, Jiaxi Xu*. Improved Buchner reaction selectivity in the copper-catalyzed reactions of ethyl 3-arylmethylamino-2-diazo-3- oxopropanoates. Tetrahedron2017, 73, 4616–4626. http://dx.doi.org/10.1016/j.tet.2017.06.029

l  2016

56.  Zhanhui Yang, Wei He, Baoxiang Cheng, Jiaxi Xu*. Stereochemistry and mechanistic insight in the [2^k + 2ⁱ + 2ⁱ] annulations of ketenes and imines. J. Org. Chem.2016, 81, 4506-4515.https://doi.org/10.1021/acs.joc.6b00279

57.  Zhanhui Yang, Wei Xu, Qiuyue Wu, and Jiaxi Xu*. Aminoxidation of Arenethiols to N-Chloro-N-sulfonyl Sulfinamides. J. Org. Chem.2016, 81, 3051–3057.https://doi.org/10.1021/acs.joc.6b00261

58.  Zhanhui Yang^#, Shili Hou^#, Wei He, Baoxiang Cheng, Peng Jiao*, Jiaxi Xu*. Regioselectivity of the ortho- and para-Semidine, and Diphenyline Rearrangements. Tetrahedron2016, 72, 2186–2195.https://doi.org/10.1016/j.tet.2016.03.019

59.  Qiuyue Wu, Zhanhui Yang*, Jiaxi Xu*. Temperature-dependent annuloselectivity and stereochemistry in the reactions of methanesulfonyl sulfene with imines. Org. Biomol. Chem.2016, 14, 7258-7267.https://doi.org/10.1039/C6OB01259K

60.  Jiandong Wang, Pingfan Li, Zhanhui Yang, Ning Chen, Jiaxi Xu*. Insights into the diastereoselective control in the sulfa-Michael addition of thiols to nitroalkenes: stereoelectronic effect in the cyclic chelated transition state. Tetrahedron2016, 72, 370–378. http://dx.doi.org/10.1016/j.tet.2015.11.030

l  Publications during PhD studies (2010-2015)

61.  Zhanhui Yang, Ning Chen, Jiaxi Xu*. Substituent-Controlled Annuloselectivity and Stereoselectivity in the Sulfa-Staudinger Cycloadditions.J. Org. Chem.2015,80, 3611–3620.https://doi.org/10.1021/acs.joc.5b00312

62.  Zhanhui Yang, Jiaxi Xu*. Annuloselectivity and Stereochemistry in the Sulfa-Staudinger Cycloadditions of Cyclic imines. RSC Adv.2015, 5, 78396–78405. https://doi.org/10.1039/C5RA15717J

63.  Zhanhui Yang, Jiaxi Xu*. Substituent Effect on the Diastereoselectivity in the Sulfa-Staudinger Cycloaddition. Tetrahedron2015, 71, 2844–2852. https://doi.org/10.1016/j.tet.2015.03.076

64.  Zhanhui Yang, Jiaxi Xu*. Synthesis of Benzo-γ-sultams via the Rh-catalyzed Aromatic C–H Functionalization of Diazosulfonamides. Chem. Commun.2014, 50, 3616–3618.https://doi.org/10.1039/C4CC00250D

65.  Zhanhui Yang, Jiaxi Xu*. Insights on β-Sultam Ring Formation in the Sulfa-Staudinger Cycloadditions. J. Org. Chem. 2014,79, 10703–10708.https://doi.org/10.1021/ar0200899

66.  Zhanhui Yang, Siqi Li, Zhong Zhang, and Jiaxi Xu*. Base-switched Annuloselectivity in the Reactions of Ethyl Malonyl Chloride and Imines. Org. Biomol. Chem.2014,12, 9822–9830.https://doi.org/10.1039/c4ob01454e

67.  Zhanhui Yang, Kwon-Il Son, Siqi Li, Bingnan Zhou, Jiaxi Xu*. Specific Hydride 1,2-Shift in Boron Trifluoride-Catalyzed Reactions of Aromatic Aldehydes with Diazoacetonitrile: Simple Synthesis of β-Ketonitriles. Eur. J. Org. Chem.2014,6380–6384.https://doi.org/10.1002/ejoc.201402901

68.  Zhanhui Yang, Bingnan Zhou, Jiaxi Xu*. Clean and Economic Synthesis of Alkanesulfonyl Chlorides from S-Alkyl Isothiourea Salts via Bleach Oxidative Chlorosulfonation. Synthesis2014, 46, 225–229.https://doi.org/10.1055/s-0033-1338567

69.  Zhanhui Yang, Jiaxi Xu*. Preparation of Alkanesulfonyl Chlorides from S-Alkyl Isothiourea Salts via N-Chlorosuccinimide Mediated Oxidative Chlorosulfonation. Org. Synth.2014, 91, 116–124. http://dx.doi.org/10.15227/orgsyn.091.0116

70.  Zhanhui Yang*.O-(2,4-Dinitrophenyl)hydroxylamine.Synlett2014, 25, 1186–1187. http://dx.doi.org/10.1055/s-0033-1341110

71.  Shanyan Mo, Zhanhui Yang, Jiaxi Xu*. Aqueous Copper Nitrate Catalyzed Synthesis of 3-Alkylideneoxindoles from α-Diazo-β-ketoanilides. Eur. J. Org. Chem. 2014, 3923–3929.https://doi.org/10.1002/ejoc.201402206

72.  Zhanhui Yang, Yongpeng Zheng, Jiaxi Xu*. Simple Synthesis of Sulfonyl Chlorides from Thiol Precusors and Derivatives by NaClO₂-Mediated Oxidative Chlorosulfonation. Synlett2013, 24, 2165–2169. https://doi.org/10.1055/s-0033-1339675

73.  Zhanhui Yang, Jiaxi Xu*. Convenient and Environment-Friendly Synthesis of Sulfonyl Chlorides from S-Alkylisothiourea Salts via N-Chlorosuccinimide Chlorosulfonation. Synthesis2013, 45, 1675–1682.https://doi.org/10.1055/s-0033-1338743

74.  Zhanhui Yang, Jiaxi Xu*. Remarkable Ketene Substituent Dependent Effect of Photo Irradiation on the Diastereoselectivity in the Staudinger Reaction. Tetrahedron Lett.2012, 53, 786–789.http://dx.doi.org/10.1016/j.tetlet.2011.12.003

75.  Hengzhen Qi, Zhanhui Yang, Jiaxi Xu*. Synthesis of 3-Alkoxy/Aryloxy- β-lactams Using Diazoacetate Esters as Ketene Precursors Under Photoirradiation. Synthesis2011, 43, 723–730. http://dx.doi.org/10.1055/s-0030-1259485

(1)   杨占会; 陈洋. 一种合成紫杉醇抗药细胞株H460_TaxR抑制剂的方法. ZL2023101526704.

(2)          杨占会; 陈宁; 徐冬. 一种制备天麻提取物2,4-双(4-羟基苄基)苯酚的方法. ZL2022116102118.

(1)     Zhanhui Yang*, Aijun Gao*. On the Chinese translations of “Pinacolyl alcohol” and “Pinacol”.Univ. Chem.2025. (in Chinsese: 杨占会*, 高爱君*. “频哪基醇”与“频哪醇”是同一物质吗？大学化学,2025). https://doi.org/10.12461/PKU.DXHX202506030

(2)     Zhanhui Yang*, Jiaxi Xu. (m + n + …) or [m + n + …] cycloaddition? Univ. Chem. 2025, 40(3): 387-389. (in Chinsese: 杨占会*, 许家喜. (m + n + …)还是[m + n + …]环加成？大学化学,2025, 40(3), 387-389.)https://doi.org/10.12461/PKU.DXHX202406032

(3)     Zhanhui Yang*, Ning Chen. Theoretical Basis and Govern Factors ofHalogenophilic Substitutions of Haloalkanes. Chin. J. Chem. Edu. 2023, 44(6): 181-184. (in Chinsese: 杨占会*, 陈宁. 卤代烷亲卤取代反应的理论基础与影响因素. 化学教育（中英文）, 2023, 44(6), 181-184.)https://doi.org/10.13884/j.1003-3807hxjy.2022020141

(4)     Zhanhui Yang*, Jiaxi Xu. Alkene Oxymercuration-Demercuration: Detailed Mechanism for Demercuration. Chin. J. Chem. Edu. 2023, 44(2), 117-122. (in Chinsese: 杨占会*, 许家喜. 烯烃的羟汞化脱汞:还原脱汞机理. 化学教育(中英文), 2023, 44(2), 117-122.)https://doi.org/10.13884/j.1003-3807hxjy.2021090184

(5)     Jiaxi Xu*, Zhanhui Yang, Yuan Ma. Why Do Vicinal and Geminal Dihaloalkanes Undergo Elimination to Afford Alkynes Rather Than Allenes. Chin. J. Chem. Edu. 2025, 46 (2), 123-125. (in Chinsese: 许家喜*, 杨占会, 麻远. 为何邻和偕二卤代烷消除反应生成炔而不是丙二烯型产物. 化学教育(中英文)2025, 46 (2): 123-125.) https://doi.org/10.13884/j.1003-3807hxjy.2024060022

(6)     Zhanhui Yang*, Yang Chen. The Boration-Migratory Addtion-Oxidation and Boration-Oxidation of 1-Alkynes. Univ. Chem.2021, 36(4), 2005028. (in Chinsese:杨占会*, 陈洋. 端炔的硼化-迁移加成-氧化和硼化-氧化. 大学化学, 2021, 36(4): 2005028.)https://doi.org/10.3866/PKU.DXHX202005028

(7)     Ziyang Dong, Zhanhui Yang, Jiaxi Xu. Indiscriminate Use of Chinese Translations of Two Alkaloids in Strychnos Nux-vomica L. and a Suggested Solution. Univ. Chem.2021, 36(4), 2005056. (in Chinsese: 董子阳, 杨占会*, 许家喜. 关于规范两种马钱子生物碱中文译名的建议. 大学化学, 2021, 36 (4): 2005056.)https://doi.org/10.3866/PKU.DXHX202005056

(8)     Zhanhui Yang*, Xufan Shen. Kekule's Structure of Benzene and the Resonance Structures of Benzene. Univ. Chem.2021, 36(8), 2009012.(in Chinsese: 杨占会*, 沈旭凡. 苯的凯库勒式与苯的共振结构. 大学化学, 2021, 36(8): 2009012.)https://doi.org/10.3866/PKU.DXHX202009012

(9)     Zhanhui Yang*, Xufan Shen. Dewar Benzene and the Resonance Structures of Benzene. Univ. Chem.2021, 36(6), 2008014.(in Chinsese: 杨占会*, 沈旭凡. 杜瓦苯与苯的共振结构. 大学化学, 2021, 36(6): 2008014.) https://doi.org/10.3866/PKU.DXHX202008014

(10)Zhanhui Yang*, Jiaxi Xu. Green Development Concept in Organic Chemistry Course. Univ. Chem. 2020, 35(7), 99-103. (in Chinsese: 杨占会*, 许家喜*. 有机化学课程中的绿色发展理念. 大学化学, 2020, 35(7): 99-103.) https://doi.org/10.3866/PKU.DXHX202003053

(11)Zhanhui Yang*, Jiaxi Xu. A Suggestion to Clarify the Chinese Descriptions on Organic Molecule Symmetries. Univ. Chem. 2020, 35(7), 181-184.(in Chinsese: 杨占会*, 许家喜. 关于区分有机分子对称性中文表述的建议. 大学化学, 2020, 35(7): 181-184.) https://doi.org/10.3866/PKU.DXHX202003104