Advances on Synthesis of Flavonoid Glycosides
- Corresponding author: Xie Jizhao, xiejizhao@gxmu.edu.cn Li Xuehua, onlythankforyou@163.com
Citation:
Xu Huanji, Li Zheming, Wu Yunqiu, Luo Di, Qiu Li, Xie Jizhao, Li Xuehua. Advances on Synthesis of Flavonoid Glycosides[J]. Chinese Journal of Organic Chemistry,
;2019, 39(7): 1875-1890.
doi:
10.6023/cjoc201811002
Zhang, T. T.; Wang, M.; Yang, L.; Jiang, J. G.; Zhao, J. W.; Zhu, W. J. Funct. Foods 2015, 18, 235.
doi: 10.1016/j.jff.2015.07.006
Shu, J.; Li, L.; Zhou, M.; Yu, J.; Peng, C.; Shao, F.; Liu, R.; Zhu, G.; Huang, H. Nat. Prod. Res. 2017, 23, 1.
Huang, X.-X.; Wei, H.-L.; Pan, Y.-F. Food Ferment. Ind. 2013, 34, 140 (in Chinese).
Ekuadzi, E.; Dickson, R.; Fleischer, T.; Annan, K.; Pistorius, D.; Oberer, L.; Gibbons, S. Phytother. Res. 2014, 28, 784.
doi: 10.1002/ptr.5053
Jiang, X.-W.; Bai, J.-P.; Tian, X.; Zhao, Q.-C. Chin. Trad. Herb. Drugs 2016, 47, 726 (in Chinese).
Shi, Q.; Guan, F.-Q.; Sun, H.; Zhao, Y.-Y.; Wang, M.; Zhang, J.-H.; Feng, X.; Shan, Y. Food Sci. Technol. 2013, (6), 220 (in Chinese).
Sun, L.; Peng, Q.; Qu, L.; Gong, L.; Si, J. Mol. Med. Rep. 2015, 11, 3094.
doi: 10.3892/mmr.2014.3007
Ekuadzi, E.; Dickson, S.; Fleischer.; Annan, K.; Pistorius, D.; Oberer, L.; Gibbons, S. Phytother. Res. 2014, 28, 784.
doi: 10.1002/ptr.5053
Nawwar, M. A.; Hashem, A. N.; Hussein, S. A.; Swilam, N. F.; Becker, A.; Haertel, B.; Lindequist, U.; El-Khatib, A.; Linscheid, M. W. Pharmazie 2016, 71, 162.
Kumamoto, H.; Matsubara, Y.; Iizuka, Y.; Okamoto, K.; Yokoi, K. Agric. Biol. Chem. 2014, 49, 2613.
Nguyen, P. H.; Dung, V. V.; Bing, T. Z.; Kim, Y. H.; Min, B. S.; Mi, H. W. Arch. Pharmacal Res. 2014, 37, 1394.
doi: 10.1007/s12272-014-0422-5
Du, X.-G.; Geng, M.-Y. Sci. Life 2011, 23, 671 (in Chinese).
Montreuil, J. Adv. Carbohydr. Chem. Biochem. 1980, 37, 157.
doi: 10.1016/S0065-2318(08)60021-9
Winterburn, P. J.; Phelps, C. F. Nature 1972, 236, 147.
doi: 10.1038/236147a0
Zhang, Y.-M. J. Northwest Univ. (Nat. Sci. Ed.) 2016, 46, 385 (in Chinese).
Ranjbari, J.; Mokhtarzadeh, A.; Alibakhshi, A.; Tabarzad, M.; Hejazi, M.; Ramezani, M. Curr. Pharm. Des. 2017, 23, 6019.
Hofer, B. Appl. Microbiol. Biotechnol. 2016, 100, 4269.
doi: 10.1007/s00253-016-7465-0
Huang, D.-D.; Chen, H.-H.; Li, M.-G.; Huang, J.-B.; Li, Y.-R.; Wei, G. Tradit. Chin. Drug Res. Pharmacol. 2017, 28, 73 (in Chinese).
Obmann, A.; Zehl, M.; Purevsuren, S.; Narantuya, S.; Reznicek, G.; Kletter, C.; Glasl, S. J. Sep. Sci. 2015, 34, 292.
Qiu, L.; Jiao, Y.; Xie, J. Z.; Huang, G. K.; Qiu, S. L.; Miao, J. H.; Yao, X. S. J. Asian Nat. Prod. Res. 2013, 16, 589.
Kondo, T.; Yoshida, K.; Oyama, K. I. Curr. Org. Chem. 2011, 15, 2567.
doi: 10.2174/138527211796367354
Wang, Z. L.; Yang, L. Y.; Yang, X. W. Synth. Commun. 2013, 43, 22.
Mei, Q.-G.; Yuan, W.-C.; Wang, C. Chin. J. Org. Chem. 2015, 35, 70 (in Chinese).
Sun, J. S.; Laval, S.; Yu, B. Synthesis 2014, 46, 1030.
doi: 10.1055/s-0033-1341052
Mohadeszadeh, M.; Iranshahi, M. Mini-Rev. Med. Chem. 2017, 17, 1377.
Kitamura, K.; Ando, Y.; Matsumoto, T.; Suzuki, K. Chem. Rev. 2018, 118, 1495.
doi: 10.1021/acs.chemrev.7b00380
Xiao, J.; Muzashvili, T. S.; Georgiev, M. I. Biotechnol. Adv. 2014, 32, 1145.
doi: 10.1016/j.biotechadv.2014.04.006
Hofer, B. Appl. Microbiol. Biotechnol. 2016, 100, 4269.
doi: 10.1007/s00253-016-7465-0
Ares, J. J.; Outt, P. E.; Kakodkar, S. V.; Buss, R. C.; Geiger, J. C. J. Org. Chem. 1993, 58, 7093.
Song, G. Y.; Ahn, B. Z. Arch. Pharmacal Res. 1994, 17, 434.
doi: 10.1007/BF02979121
Wang, Q.-A.; Liao, T.-G.; Tang, J.-G.; Fan, H.-F. J. Hunan Univ. (Nat. Sci.) 2004, 31, 1 (in Chinese).
Zacharia, J. T.; Hayashi, M. Carbohydr. Res. 2012, 348, 91.
doi: 10.1016/j.carres.2011.11.015
Kerl, T.; Berger, F.; Schmalz, H. G. Chemistry 2016, 22, 2935.
doi: 10.1002/chem.201505118
Algarl, J.; Flynn, J. P. Proc. R. Ir. Acad. 1934, 42, 1.
Oyamada. B. Chem. Soc. Jpn. 1934, 55, 2039.
Oyamada, T. Tetrahedron 1935, 64, 988.
Zhou, Q.; Wang, C.; Li, Y.-P.; Pu, W.-C. Chin. J. Appl. Environ. Biol. 2017, 24, 232 (in Chinese).
Shen, X.; Zhou, Q.; Xiong, W.; Pu, W.; Zhang, W.; Zhang, G.; Wang, C. Tetrahedron 2017, 73, 4822.
doi: 10.1016/j.tet.2017.06.064
Li, X.; Chen, G.; Zhang, X.; Zhang, Q.; Zheng, S.; Wang, G.; Chen, Q. H. Bioorg. Med. Chem. Lett. 2016, 26, 4241.
doi: 10.1016/j.bmcl.2016.07.050
Wang, Q.-A.; Wang, S.-C.; Li, Y.; Shan, Y. J. Hunan Univ. (Nat. Sci.) 2015, 42, 53 (in Chinese).
Zhang, J.; Fu, X. L.; Yang, N.; Wang, Q. A. Sci. World J. 2013, 2013, 649485.
Jian, J.; Fan, J.; Yang, H.; Lan, P.; Li, M.; Liu, P.; Gao, H.; Sun, P. J. Nat. Prod. 2018, 81, 371.
doi: 10.1021/acs.jnatprod.7b00791
Yamauchi, K.; Mitsunaga, T.; Batubara, I. Bioorg. Med. Chem. 2014, 22, 937.
doi: 10.1016/j.bmc.2013.12.062
Liang, G.; Xu, B.; Wen, Z.; Hu, Z.; Yuan, J.; Chen, H.; Zhang, L. Heterocycles. 2016, 92, 1245.
doi: 10.3987/COM-16-13455
Xue, X.-N. Chem. Reag. 2018, 40, 465 (in Chinese).
Liu, J. D; Chen, L.; Cai, S. C.; Wang, Q. A. Carbohydr. Res. 2012, 357, 41.
doi: 10.1016/j.carres.2012.05.013
Park, K. S.; Kim, H.; Mi K. K.; Kim, K.; Chong, Y. J. Korean Soc. Appl. Biol. Chem. 2015, 58, 317.
Yang, W.; Sun, J.; Yang, Z.; Han, W.; Zhang, W. D., Yu B. Tetrahedron Lett. 2012, 43, 2773.
Yang, W.; Sun J.; Lu, W.; Li, Y.; Shan, L.; Han, W.; Zhang, W.; Yu, B. J. Org. Chem. 2010, 75, 6879.
doi: 10.1021/jo1014189
Mei, Q.; Wang, C. Z.; Yuan, W.; Zhang, G. Beilstein J. Org. Chem. 2015, 11, 1220.
doi: 10.3762/bjoc.11.135
Chen, J.; Huang, W.; Lian, G.; Lin, F. Carbohydr. Res. 2009, 344, 2245.
doi: 10.1016/j.carres.2009.08.014
Koenigs, W., Knorr, E. Eur. J. Inorg. Chem. 2010, 34, 957.
Zhao, J.; Zhang, Z.-P.; Chen, H.-S.; Zhang, X.-Q.; Chen, X.-H. Acta Pharm. Sin. 1998, 33, 22 (in Chinese).
Vermes, B.; Farkas, L.; Nógrádi, M.; Wagner, H.; Dirscherl, R. Phytochemistry 1976, 15, 1320.
doi: 10.1016/0031-9422(76)85106-0
Farkas, L.; Nógr di, M.; Vermes, B.; Wolfner, A.; Wagner, H.; Hörhammer, L.; Krämer, H. Eur. J. Inorg. Chem. 1969, 102, 2583.
Mezey-Vandor, G.; Farkas, L.; Kanzel, I.; Ndgradi, M. Chem. Ber. 1980, 113, 1945.
doi: 10.1002/cber.19801130529
Docampo, M.; Olubu, A.; Wang, X. Q.; Pasinetti, G.; Dixon, R. A. J. Agric. Food Chem. 2017, 65, 7607.
doi: 10.1021/acs.jafc.7b02633
Huang, W. H.; Chien, P. Y.; Yang, C. H.; Lee, A. R. Chem. Pharm. Bull. 2003, 34, 339.
Li, Y. F.; Yu, B.; Sun, J. S.; Wang, R. X. Tetrahedron Lett. 2015, 56, 3816.
doi: 10.1016/j.tetlet.2015.04.083
Demetzos, C.; Skaltsounis, A. L.; Tillequin, F.; Koch, M. Planta Med. 1990, 207, 131.
Wang, Q.-A.; Wu, Z.; Liu, L.; Zou, L.-H.; Luo, M. Chin. J. Org. Chem. 2010, 30, 1682 (in Chinese).
Cao, Z. L.; Qu, Y. Y.; Zhou, J. X.; Liu, W. W.; Yao, G. W. J. Carbohydr. Chem. 2015, 34, 28.
doi: 10.1080/07328303.2014.996290
Cao, Z. L.; Chen, J.; Zhu, D. D.; Yang, Z. N.; Teng, W. Q.; Liu, G. F.; Liu, B.; Tao, C. Z. J. Chem. Res. 2018, 42, 189.
doi: 10.3184/174751918X15232706115112
Nakagawa, A.; Tanaka, M.; Hanamura, S.; Takahashi, D.; Toshima, K. Angew. Chem., Int. Ed. 2015, 54, 10935.
doi: 10.1002/anie.201504182
Du, Y.; Wei, G.; Lindhardt, R. J. Tetrahedron Lett. 2003, 44, 6887.
doi: 10.1016/S0040-4039(03)01706-4
Arai, M. A.; Yamaguchi, Y.; Ishibashi, M. Org. Biomol. Chem. 2017, 15, 5025.
doi: 10.1039/C7OB01004D
Zou, L.; Zhang, Z.; Chen, X.; Chen, H.; Zhang, Y.; Li, J.; Liu, Y. Tetrahedron 2018, 74, 2376.
doi: 10.1016/j.tet.2018.03.057
Liao, J. X.; Fan, N. L.; Liu, H.; Tu, Y. H.; Sun, J. S. Org. Biomol. Chem. 2015, 14, 1221.
Hu, Y.; Tu, Y. H.; Liu, D. Y.; Liao, J. X.; Sun, J. S. Org. Biomol. Chem. 2016, 14, 4842.
doi: 10.1039/C6OB00655H
Yang, W.-Z.; Li, R.-Y.; Han, W.; Zhang, W.-D.; Sun, J.-S. Chin. J. Org. Chem. 2012, 32, 1067 (in Chinese).
Carte, B. K.; Carr, S.; Debrosse, C.; Hemling, M. E.; Mackenzie, L.; Offen, P.; Berry, D. E. ChemInform 1991, 22, 1815.
Lai, C. Y.; Tsai, A. C.; Chen, M. C.; Chang, L. H.; Sun, H. L.; Chang, Y. L.; Chen, C. C.; Teng, C. M.; Pan, S. L. Plos One 2012, 7, e42192.
doi: 10.1371/journal.pone.0042192
Hsieh, I.; Chang, S. Y.; Teng, C. M.; Chen, C. C.; Yang, C. R. J. Biomed. Sci. 2011, 18, 28.
doi: 10.1186/1423-0127-18-28
Yao, C. H.; Tsai, C. H.; Lee, J. C. J. Nat. Prod. 2016, 79, 1719.
doi: 10.1021/acs.jnatprod.5b01051
Wang, Y.; Liu, M.; Liu, L.; Xia, J. H.; Du, Y. G.; Sun, J. S. J. Org. Chem. 2018, 83, 4111.
doi: 10.1021/acs.joc.8b00008
Yang, D.; Zhang, X.; Zhang, W.; Rengarajan, T. Drug Des., Dev. Ther. 2018, 12, 1303.
doi: 10.2147/DDDT.S149307
Ku, S. K.; Bae, J. S. Can. J. Physiol. Pharmacol. 2016, 94, 287.
doi: 10.1139/cjpp-2015-0215
Shie, J. J.; Chen, C. A.; Lin, C. C.; Ku, A. F.; Cheng, T. J.; Fang, J. M.; Wong, C. H. Org. Biomol. Chem. 2010, 8, 4451.
doi: 10.1039/c0ob00011f
Sato, S.; Akiya, T.; Nishizawa, H.; Suzuki, T. Carbohydr. Res. 2006, 341, 964.
doi: 10.1016/j.carres.2006.02.019
Ho, T. C.; Kamimura, H.; Ohmori, K.; Suzuki, K. Org. Lett. 2016, 18, 4488.
doi: 10.1021/acs.orglett.6b02203
Mao, D.-B.; Huang, S.-L.; Chen, Y.-S. China Surf. Deterg. Cosmet. 2007, 37, 321 (in Chinese).
doi: 10.3969/j.issn.1001-1803.2007.05.011
Hofer, B. Appl. Microbiol. Biotechnol. 2016, 100, 4269.
doi: 10.1007/s00253-016-7465-0
Choung, W. J.; Hwang, S. H.; Ko, D. S.; Kim, S. B.; Kim, S. H.; Jeon. S. H.; Choi, H. D.; Lim, S. S.; Shim, J. H. J. Agric. Food Chem. 2017, 65, 2760.
doi: 10.1021/acs.jafc.7b00501
Kim, S. Y.; Lee, H. R.; Park, K. S.; Kim, B. G.; Ahn, J. H. Appl. Microbiol. Biotechnol. 2015, 99, 2233.
doi: 10.1007/s00253-014-6282-6
Liang, C.; Zhang, Y.; Jia, Y.; Wang, W.; Li, Y.; Lu, S.; Jin, J. M.; Tang, S. Y. Sci Rep. 2016, 6, 21051.
doi: 10.1038/srep21051
Pandey, R. P.; Parajuli, P.; Koirala, N.; Park, J. W.; Sohng, J. K. Appl. Environ. Microbiol. 2013, 79, 6833.
doi: 10.1128/AEM.02057-13
Gurung, R. B.; Kim, E. H.; Oh, T. J.; Sohng, J. K. Mol. Cells 2013, 36, 355.
doi: 10.1007/s10059-013-0164-0
Liu, X. G.; Lin, C. L.; Ma, X. D.; Yan, Y.; Wang, J. Z.; Zeng, M. Front. Recent Dev. Plant Sci. 2018, 9, 166.
doi: 10.3389/fpls.2018.00166
Feng, J.; Zhang, P.; Cui, Y.; Li, K.; Qiao, X.; Zhang, Y. T.; Li, S. M.; Cox, R. J.; Wu, B.; Ye, M. Adv. Synth. Catal. 2017, 359, 955.
Han, S. H.; Kim, B. G.; Yoon, J. A.; Chong, Y.; Ahn, J. H. Appl. Environ. Microbiol. 2014, 80, 2754.
doi: 10.1128/AEM.03797-13
Pandey, R. P.; Parajuli, P.; Gurung, R. B.; Sohng, J. K. Enzyme Microb. Technol. 2016, 91, 26.
doi: 10.1016/j.enzmictec.2016.05.006
Simkhada, D.; Lee, H. C.; Sohng, J. K. Biotechnol. Bioeng. 2010, 107, 154.
doi: 10.1002/bit.22782
Kim, B. G.; Su, H. S.; Ahn, J. H. Appl. Microbiol. Biotechnol. 2012, 93, 2447.
doi: 10.1007/s00253-011-3747-8
Brazierhicks, M.; Evans, K. M.; Gershater, M. C.; Puschmann, H.; Steel, P. G.; Edwards, R. J. Biol. Chem. 2009, 284, 17926.
doi: 10.1074/jbc.M109.009258
Du, Y.; Chu, H.; Chu, I. K.; Lo, C. Plant Physiol. 2010, 154, 324.
doi: 10.1104/pp.110.161042
Sasaki, N.; Nishizaki, Y.; Yamada, E.; Tatsuzawa, F.; Nakatsuka, T.; Takahashi, H.; Nishihara, M. FEBS Lett. 2016, 589, 182.
Shrestha, A.; Pandey, R. P.; Dhakal, D.; Parajuli, P.; Sohng, J. K. Appl. Microbiol. Biotechnol. 2018, 102, 1251.
doi: 10.1007/s00253-017-8694-6
Vanegas, K. G.; Larsen, A. B.; Eichenberger, M.; Fischer, D.; Mortensen, U. H.; Naesby, M. Microb. Cell Fact. 2018, 17, 107.
doi: 10.1186/s12934-018-0952-5
Du, Y.; Chu, H.; Wang, M.; Chu, I. K.; Lo, C. J. Exp. Bot. 2010, 61, 983.
doi: 10.1093/jxb/erp364
Morohashi, K.; Grotewold, E. Plant Cell. 2012, 24, 2745.
doi: 10.1105/tpc.112.098004
Hirade, Y.; Kotoku, N.; Terasaka, K.; Saijo-Hamano, Y.; Fukumoto, A.; Mizukami, H. FEBS Lett. 2015, 589, 1778.
doi: 10.1016/j.febslet.2015.05.010
Gutmann, A.; Nidetzky, B. Pure Appl. Chem. 2013, 85, 1865.
doi: 10.1351/pac-con-12-11-24
Hao, B.; Caulfield, J. C.; Hamilton, M. L.; Pickett, J. A.; Midega, C. A.; Khan, Z. R.; Wang, J. R. Org. Biomol. Chem. 2015, 13, 11663.
doi: 10.1039/C5OB01926E
Ito, T.; Fujimoto, S.; Suito, F.; Shimosaka, M.; Taguchi, G. Plant J. Cell Mol. Biol. 2017, 91, 187.
doi: 10.1111/tpj.13555
Nagatomo, Y.; Usui, S.; Ito, T.; Kao, A.; Shimosaka, M.; Taguchi, G. Plant J. 2014, 80, 437.
doi: 10.1111/tpj.12645
Mackenzie, L. F.; Wang, Q.; Warren, R. A. J.; Withers, S. G. J. Am. Chem. Soc. 1998, 120, 5583.
doi: 10.1021/ja980833d
Malet, C.; Planas, A. FEBS Lett. 1998, 440, 208.
doi: 10.1016/S0014-5793(98)01448-3
Moracci, M.; Trincone, A.; Perugino, G.; Ciaramella, M.; Rossi, M. Biochemistry 1998, 37, 17262.
doi: 10.1021/bi981855f
Hayes, M. R.; Pietruszka, J. Molecules 2017, 22, 1434.
doi: 10.3390/molecules22091434
Kobayashi, S.; Shoda, S.; Uyama, H. Adv. Polym. Sci. 2012, 121, 217.
Díez-Municio, M.; Kolida, S.; Herrero, M.; Rastall, R. A.; Moreno, F. J. J. Funct. Foods 2016, 20, 532.
doi: 10.1016/j.jff.2015.11.032
Ducros, V. M.; Tarling, C. A.; Zechel, D. L.; Brzozowski, A. M., Frandsen, T. P.; Ossowski, I. V.; Schülein, M.; Withers, S. G.; Davies, G. J. Chem. Biol. 2003, 10, 619.
doi: 10.1016/S1074-5521(03)00143-1
Yang, M.; Davies, G. J.; Davis, B. G. Angew. Chem. 2007, 46, 3885.
doi: 10.1002/anie.200604177
Jing WU , Puzhen HUI , Huilin ZHENG , Pingchuan YUAN , Chunfei WANG , Hui WANG , Xiaoxia GU . Synthesis, crystal structures, and antitumor activities of transition metal complexes incorporating a naphthol-aldehyde Schiff base ligand. Chinese Journal of Inorganic Chemistry, 2024, 40(12): 2422-2428. doi: 10.11862/CJIC.20240278
Xinting XIONG , Zhiqiang XIONG , Panlei XIAO , Xuliang NIE , Xiuying SONG , Xiuguang YI . Synthesis, crystal structures, Hirshfeld surface analysis, and antifungal activity of two complexes Na(Ⅰ)/Cd(Ⅱ) assembled by 5-bromo-2-hydroxybenzoic acid ligands. Chinese Journal of Inorganic Chemistry, 2024, 40(9): 1661-1670. doi: 10.11862/CJIC.20240145
Jiaming Xu , Yu Xiang , Weisheng Lin , Zhiwei Miao . Research Progress in the Synthesis of Cyclic Organic Compounds Using Bimetallic Relay Catalytic Strategies. University Chemistry, 2024, 39(3): 239-257. doi: 10.3866/PKU.DXHX202309093
Yukun Chang , Haoqin Huang , Baolei Wang . Preparation of Trans-Cinnamic Acid via “One-Pot” Protocol of Aldol Condensation-Hydrolysis Reaction: Recommending an Improved Organic Synthesis Experiment. University Chemistry, 2024, 39(4): 322-328. doi: 10.3866/PKU.DXHX202309095
.
CCS Chemistry 综述推荐│绿色氧化新思路:光/电催化助力有机物高效升级
. CCS Chemistry, 2025, 7(10.31635/ccschem.024.202405369): -.Yifan Liu , Haonan Peng . AI-Assisted New Era in Chemistry: A Review of the Application and Development of Artificial Intelligence in Chemistry. University Chemistry, 2025, 40(7): 189-199. doi: 10.12461/PKU.DXHX202405182
Hong Lu , Yidie Zhai , Xingxing Cheng , Yujia Gao , Qing Wei , Hao Wei . Advancements and Expansions in the Proline-Catalyzed Asymmetric Aldol Reaction. University Chemistry, 2024, 39(5): 154-162. doi: 10.3866/PKU.DXHX202310074
Yang YANG , Pengcheng LI , Zhan SHU , Nengrong TU , Zonghua WANG . Plasmon-enhanced upconversion luminescence and application of molecular detection. Chinese Journal of Inorganic Chemistry, 2024, 40(5): 877-884. doi: 10.11862/CJIC.20230440
Minna Ma , Yujin Ouyang , Yuan Wu , Mingwei Yuan , Lijuan Yang . Green Synthesis of Medical Chemiluminescence Reagents by Photocatalytic Oxidation. University Chemistry, 2024, 39(5): 134-143. doi: 10.3866/PKU.DXHX202310093
Qingying Gao , Tao Luo , Jianyuan Su , Chaofan Yu , Jiazhu Li , Bingfei Yan , Wenzuo Li , Zhen Zhang , Yi Liu . Refinement and Expansion of the Classic Cinnamic Acid Synthesis Experiment. University Chemistry, 2024, 39(5): 243-250. doi: 10.3866/PKU.DXHX202311074
Wenjun Zheng . Application in Inorganic Synthesis of Ionic Liquids. University Chemistry, 2024, 39(8): 163-168. doi: 10.3866/PKU.DXHX202401020
Hongyan Chen , Yajun Hou , Shui Hu , Zhuoxun Wei , Fang Zhu , Chengyong Su . Construction of Synthetic Chemistry Experiment of the Chemistry “101 Plan”. University Chemistry, 2024, 39(10): 58-63. doi: 10.12461/PKU.DXHX202409109
Huijuan Liao , Yulin Xiao , Dong Xue , Mingyu Yang , Jianyang Dong . Synthesis of 1-Benzyl Isoquinoline via the Minisci Reaction. University Chemistry, 2025, 40(7): 294-299. doi: 10.12461/PKU.DXHX202409092
Cunming Yu , Dongliang Tian , Jing Chen , Qinglin Yang , Kesong Liu , Lei Jiang . Chemistry “101 Program” Synthetic Chemistry Experiment Course Construction: Synthesis and Properties of Bioinspired Superhydrophobic Functional Materials. University Chemistry, 2024, 39(10): 101-106. doi: 10.12461/PKU.DXHX202408008
Jiaojiao Yu , Bo Sun , Na Li , Cong Wen , Wei Li . Improvement of Classical Organic Experiment Based on the “Reverse-Step Optimization Method”: Taking Synthesis of Ethyl Acetate as an Example. University Chemistry, 2025, 40(3): 333-341. doi: 10.12461/PKU.DXHX202405177
Yanglin Jiang , Mingqing Chen , Min Liang , Yige Yao , Yan Zhang , Peng Wang , Jianping Zhang . Experimental and Theoretical Investigations of Solvent Polarity Effect on ESIPT Mechanism in 4′-N,N-diethylamino-3-hydroxybenzoflavone. Acta Physico-Chimica Sinica, 2025, 41(2): 100012-. doi: 10.3866/PKU.WHXB202309027
Yuan Zheng , Quan Lan , Zhenggen Zha , Lingling Li , Jun Jiang , Pingping Zhu . Teaching Reform of Organic Synthesis Experiments by Introducing Reverse Thinking and Design Concepts: Taking the Synthesis of Cinnamic Acid Based on Retrosynthetic Analysis as an Example. University Chemistry, 2024, 39(6): 207-213. doi: 10.3866/PKU.DXHX202310065
Li Jiang , Changzheng Chen , Yang Su , Hao Song , Yanmao Dong , Yan Yuan , Li Li . Electrochemical Synthesis of Polyaniline and Its Anticorrosive Application: Improvement and Innovative Design of the “Chemical Synthesis of Polyaniline” Experiment. University Chemistry, 2024, 39(3): 336-344. doi: 10.3866/PKU.DXHX202309002
Yinwu Su , Xuanwen Zheng , Jianghui Du , Boda Li , Tao Wang , Zhiyan Huang . Green Synthesis of 1,3-Dibromoacetone Using Halogen Exchange Method: Recommending a Basic Organic Synthesis Teaching Experiment. University Chemistry, 2024, 39(5): 307-314. doi: 10.3866/PKU.DXHX202311092
Jianbao Mei , Bei Li , Shu Zhang , Dongdong Xiao , Pu Hu , Geng Zhang . Enhanced Performance of Ternary NASICON-Type Na3.5-xMn0.5V1.5-xZrx(PO4)3/C Cathodes for Sodium-Ion Batteries. Acta Physico-Chimica Sinica, 2024, 40(12): 2407023-. doi: 10.3866/PKU.WHXB202407023