Recent advances on cyclization reaction of indole-tethered alkenes for the construction of polyheterocycles
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* Corresponding authors.
E-mail addresses: kiss.lorand@ttk.hu (L. Kiss), hanjl@njfu.edu.cn (J. Han).
Citation:
Haibo Mei, Anas Semghouli, Loránd Kiss, Jianlin Han. Recent advances on cyclization reaction of indole-tethered alkenes for the construction of polyheterocycles[J]. Chinese Chemical Letters,
;2026, 37(8): 112405.
doi:
10.1016/j.cclet.2026.112405
S.M. Umer, M. Solangi, K.M. Khan, R.S.Z. Saleem, Molecules 27 (2022) 7586.
doi: 10.3390/molecules27217586
X. Mo, D.P. Rao, K. Kaur, et al., Molecules 29 (2024) 4770.
doi: 10.3390/molecules29194770
S. Fernández, V. Arnáiz, D. Rufo, Y. Arroyo, Mar. Drugs 22 (2024) 126.
doi: 10.3390/md22030126
A. Dorababu, RSC Med. Chem. 11 (2020) 1335–1353.
doi: 10.1039/d0md00288g
V.M. Norwood IV, R.W. Huigens Ⅲ, ChemBioChem 20 (2019) 2273–2297.
doi: 10.1002/cbic.201800768
W. Zeng, C. Han, S. Mohammed, et al., RSC Med. Chem. 15 (2024) 788–808.
doi: 10.1039/d3md00677h
Z. Zhu, S. Lu, W. Chen, J. Agric. Food Chem. 73 (2025) 22979–22993.
doi: 10.1021/acs.jafc.5c04293
M.J. Nieto, H.K. Lupton, Curr. Med. Chem. 28 (2021) 4828–4844.
doi: 10.2174/0929867327666201102114923
T. Yu, W. Liu, B. Chen, et al., Org. Lett. 27 (2025) 1459–1464.
doi: 10.1021/acs.orglett.4c04814
L. Fan, X. Zhu, X. Liu, et al., Molecules 28 (2023) 1647.
doi: 10.3390/molecules28041647
J.Y. Kim, W. Lee, H.J. Kang, et al., ACS Catal. 11 (2021) 12821–12832.
doi: 10.1021/acscatal.1c03797
A.N. Singh Chauhan, G. Mali, G. Dua, et al., ACS Omega 8 (2023) 27894–27919.
doi: 10.1021/acsomega.3c02510
Y.S. Zhang, X.Y. Tang, M. Shi, Org. Chem. Front. 2 (2015) 1516–1520.
doi: 10.1039/C5QO00216H
B.A. Babalola, M. Malik, O. Olowokere, A. Adebesin, L. Sharma, Eur. J. Med. Chem. Rep. 13 (2025) 100252.
S. Das, ACS Omega 9 (2024) 36023–36042.
M. Friedman, Int. J. Tryptophan Res. 11 (2018) 1178646918802282.
doi: 10.1177/1178646918802282
G.E. Zúñiga, M.S. Salgado, L.J. Corcuera, Phytochemistry 24 (1985) 945–947.
doi: 10.1016/S0031-9422(00)83158-1
Y. Ren, K. DeRose, L. Li, et al., Bioorg. Med. Chem. 92 (2023) 117439.
doi: 10.1016/j.bmc.2023.117439
J.C. Alves, ISRN Org. Chem. 2013 (2013) 292396.
J.F. Liu, Z.Y. Jiang, R.R. Wang, et al., Org. Lett. 9 (2007) 4127–4129.
doi: 10.1021/ol701540y
M.B. Calvert, J. Sperry, Chem. Commun. 51 (2015) 6202–6205.
doi: 10.1039/C5CC00380F
F.G. Gervais, J.P. Morello, C. Beaulieu, et al., Mol. Pharmacol. 67 (2005) 1834–1839.
doi: 10.1124/mol.104.009068
M. Ghavami, E.F. Merino, Z.K. Yao, et al., ACS Infect. Dis. 4 (2017) 549–559.
M. Tanaka, M. Ubukata, T. Matsuo, et al., Org. Lett. 9 (2007) 3331–3334.
doi: 10.1021/ol071336h
Y. Miyashita, R. Ko, N. Shimada, et al., Thorac. Cancer 12 (2021) 329–338.
doi: 10.1111/1759-7714.13742
S. Peters, D.R. Camidge, A.T. Shaw, et al., N. Engl. J. Med. 377 (2017) 829–838.
doi: 10.1056/NEJMoa1704795
P. Tfelt-Hansen, Cephalalgia 41 (2021) 1499–1505.
doi: 10.1177/03331024211028959
C. Dahlöf, H.C. Diener, P.J. Goadsby, et al., Eur. J. Neurol. 5 (1998) 535–543.
doi: 10.1046/j.1468-1331.1998.560535.x
J. Treat, A. Greenspan, A. Rahman, M.S. McCabe, P.J. Byrne, Invest. New Drugs 7 (1989) 231–234.
doi: 10.1007/BF00170864
G.V. Frajese, F. Pozzi, G. Frajese, Clin. Interv. Aging 1 (2006) 439–449.
doi: 10.2147/ciia.2006.1.4.439
J.L. Li, Q. Zhao, C. Guo, et al., Adv. Synth. Catal. 363 (2021) 4497–4515.
doi: 10.1002/adsc.202100714
Y.C. Zhang, F. Jiang, F. Shi, Acc. Chem. Res. 53 (2020) 425–446.
doi: 10.1021/acs.accounts.9b00549
B. Baruah, C.D. Pegu, M.L. Deb, Topics Curr. Chem. 382 (2024) 18.
doi: 10.1007/s41061-024-00463-y
J.S.S. Neto, G. Zeni, Org. Chem. Front. 7 (2020) 155–210.
doi: 10.1039/c9qo01315f
A. Palmieri, M. Petrini, Adv. Synth. Catal. 367 (2025) e202401237.
doi: 10.1002/adsc.202401237
M. Shiri, Chem. Rev. 112 (2012) 3508–3549.
doi: 10.1021/cr2003954
F. Feng, S. Xu, X. Wang, et al., Chin. J. Org. Chem. 45 (2025) 52632017.
J. Bariwal, L.G. Voskressensky, E.V. Van der Eycken, Chem. Soc. Rev. 47 (2018) 3831–3848.
doi: 10.1039/c7cs00508c
W. Wang, Y. Xu, X. Liao, Tetrahedron Lett. 156 (2025) 155451.
doi: 10.1016/j.tetlet.2024.155451
M. Petrini, Chem. Eur. J. 23 (2017) 16115–16151.
doi: 10.1002/chem.201702124
J. Shao, J. Liu, H. Mei, J. Han, Tetrahedron 173 (2025) 134467.
doi: 10.1016/j.tet.2025.134467
Y. Du, A. Semghouli, H. Mei, L. Kiss, J. Han, Adv. Synth. Catal. 366 (2024) 3050–3084.
doi: 10.1002/adsc.202400306
H. Mei, K. Aradi, L. Kiss, J. Han, Chin. Chem. Lett. 34 (2023) 108657.
doi: 10.1016/j.cclet.2023.108657
D. Bag, S. Sawant, Chem. Eur. J. 27 (2021) 1165–1218.
doi: 10.1002/chem.202002154
Y. Tang, K. Dai, X. Xiang, Y. Yang, M. Li, Org. Biomol. Chem. 20 (2022) 5704–5711.
doi: 10.1039/d2ob00934j
J.R. Zhang, H.Y. Liu, T. Fan, Y.Y. Chen, Y.L. Xu, Adv. Synth. Catal. 363 (2021) 497–504.
doi: 10.1002/adsc.202000983
Y. Luo, T. Tian, Y. Nishihara, L. Lv, Z. Li, Chem. Commun. 57 (2021) 9276–9279.
doi: 10.1039/d1cc03907e
P. Zhao, Y. Wang, X. Wang, D. Zhuang, R. Yan, J. Org. Chem. 87 (2022) 9056–9068.
doi: 10.1021/acs.joc.2c00735
F.L. Zeng, K. Sun, X.L. Chen, et al., Adv. Synth. Catal. 361 (2019) 5176–5181.
doi: 10.1002/adsc.201901016
B. Zhao, G.B. Hammond, B. Xu, J. Org. Chem. 86 (2021) 12851–12861.
doi: 10.1021/acs.joc.1c01486
H.C. Li, K. Sun, X. Li, et al., J. Org. Chem. 86 (2021) 9055–9066.
doi: 10.1021/acs.joc.1c01022
X. Yuan, X. Duan, Y.S. Cui, et al., Org. Lett. 23 (2021) 1950–1954.
doi: 10.1021/acs.orglett.1c00476
H. Cui, C. Niu, C. Zhang, J. Org. Chem. 86 (2021) 15835–15844.
doi: 10.1021/acs.joc.1c02027
B. Qin, S. Huang, J.Q. Chen, W. Xiao, J. Wu, Org. Chem. Front. 9 (2022) 3521–3526.
doi: 10.1039/d2qo00487a
X. Yuan, J. Liu, L.Z. Qin, et al., Adv. Synth. Catal. 365 (2023) 555–567.
doi: 10.1002/adsc.202201294
S. Bag, S. Ojha, S. Venugopalan, B. Sahoo, J. Org. Chem. 88 (2023) 12121–12130.
doi: 10.1021/acs.joc.3c01149
Y. Tang, J. Duan, B. Yang, et al., Org. Biomol. Chem. 21 (2023) 8152–8161.
doi: 10.1039/d3ob01289a
X.Q. Liu, Y. Guo, W.Q. Yu, J. Org. Chem. 88 (2023) 9293–9305.
doi: 10.1021/acs.joc.3c00863
G.C. Upreti, T. Singh, D. Chaudhary, A. Singh, J. Org. Chem. 88 (2023) 11801–11808.
doi: 10.1021/acs.joc.3c01090
G.C. Upreti, T. Singh, K. Khanna, A. Singh, J. Org. Chem. 88 (2023) 4422–4433.
doi: 10.1021/acs.joc.2c03028
Q.Q. Kang, W.K. Zhang, G.P. Ge, H. Zheng, W.T. Wei, Org. Biomol. Chem. 19 (2021) 8874–8885.
doi: 10.1039/d1ob01465j
Q.G. Mei, Q.H. Li, Tetrahedron 160 (2024) 134050.
doi: 10.1016/j.tet.2024.134050
Z. Lei, F. Xue, B. Wang, et al., Chin. Chem. Lett. 35 (2024) 108633.
doi: 10.1016/j.cclet.2023.108633
H. Mei, Y. Zhang, J. Liu, et al., Adv. Synth. Catal. 367 (2025) e202401225.
doi: 10.1002/adsc.202401225
H. Yang, Q. Yang, Y. Yao, et al., Org. Lett. 26 (2024) 6341–6346.
doi: 10.1021/acs.orglett.4c01967
Y. Li, X. Li, Z. Zhang, et al., Sci. China Chem. 68 (2025) 670–678.
doi: 10.1007/s11426-024-2214-0
A. Arribas, M. Calvelo, A. Rey, J.L. Mascarenas, F. Lopez, Angew. Chem. Int. Ed. 63 (2024) e202408258.
doi: 10.1002/anie.202408258
P. Kumar, A. Rai, M. Kumar, G. Rama Krishna, U. Das, J. Org. Chem. 88 (2023) 9123–9129.
doi: 10.1021/acs.joc.3c00759
H. Qin, Y. Zhang, S. Sun, Tetrahedron Lett. 157 (2025) 155468.
doi: 10.1016/j.tetlet.2025.155468
M. Zhu, X.L. Huang, S. Sun, C. Zheng, S.L. You, J. Am. Chem. Soc. 143 (2021) 13441–13449.
doi: 10.1021/jacs.1c07082
L. Yin, Y. Wang, M. Sun, et al., Adv. Synth. Catal. 358 (2016) 1093–1102.
doi: 10.1002/adsc.201501116
C.R. Reddy, R.R. Valleti, U. Dilipkumar, Chem. Eur. J. 22 (2016) 2501–2506.
doi: 10.2166/wst.2016.112
J.W. Ren, Z.F. Zhou, J.A. Xiao, H. Yang, Eur. J. Org. Chem. 2016 (2016) 1264–1268.
doi: 10.1002/ejoc.201501619
S.J. Liu, X.C. Liu, S.N. Wen, et al., Org. Chem. Front. 11 (2024) 3397–3403.
doi: 10.1039/d4qo00256c
X. Han, X. Lu, Org. Lett. 11 (2009) 2381–2384.
doi: 10.1021/ol9007348
X. Han, R.A. Widenhoefer, Org. Lett. 8 (2006) 3801–3804.
doi: 10.1021/ol061441b
C. Liu, R.A. Widenhoefer, J. Am. Chem. Soc. 126 (2004) 10250–10251.
doi: 10.1021/ja046810i
C. Liu, R.A. Widenhoefer, Chem. Eur. J. 12 (2006) 2371–2382.
doi: 10.1002/chem.200500787
D. Bag, S.D. Sawant, Org. Lett. 24 (2022) 4930–4934.
doi: 10.1021/acs.orglett.2c01845
M. Solas, M.A. Muñoz-Torres, F. Martínez-Lara, ChemPlusChem 88 (2023) e202300382.
doi: 10.1002/cplu.202300382
N. Inprung, H.E. Ho, J.A. Rossi-Ashton, et al., Org. Lett. 24 (2022) 668–674.
doi: 10.1021/acs.orglett.1c04098
J. He, X. Zhou, H. Mei, Chem. Commun. 61 (2025) 7454–7457.
doi: 10.1039/d5cc01342a
C.H. Oh, H.S. Park, N. Park, S.Y. Kim, L. Piao, Synlett 25 (2014) 579–585.
doi: 10.3904/kjm.2014.87.5.579
C. Ferrer, C.H.M. Amijs, A.M. Echavarren, Chem. Eur. J. 13 (2007) 1358–1373.
doi: 10.1002/chem.200601324
P.A. Grieco, M.D. Kaufman, J. Org. Chem. 64 (1999) 7586–7593.
doi: 10.1021/jo9909960
S.J. Markey, W. Lewis, C.J. Moody, Org. Lett. 15 (2013) 6306–6308.
doi: 10.1021/ol403191k
M. Abualnaja, P.G. Waddell, W. Clegg, M.J. Hall, Tetrahedron 72 (2016) 5798–5806.
doi: 10.1016/j.tet.2016.08.008
F. Taenzler, J. Xu, S. Athe, V.H. Rawal, Org. Lett. 24 (2022) 8109–8114.
doi: 10.1021/acs.orglett.2c02983
S. Xing, L. Jin, F. Jiang, et al., J. Org. Chem. 90 (2025) 7818–7831.
doi: 10.1021/acs.joc.5c00683
T. Mino, T. Yamaoka, K. Watanabe, et al., J. Org. Chem. 87 (2022) 7365–7377.
doi: 10.1021/acs.joc.2c00588
S. Cacchi, G. Fabrizi, P. Pace, J. Org. Chem. 63 (1998) 1001–1011.
doi: 10.1021/jo971237p
M. Kimura, M. Futamata, R. Mukai, Y. Tamaru, J. Am. Chem. Soc. 127 (2005) 4592–4593.
doi: 10.1021/ja0501161
K. Watanabe, K. Nakano, H. Sato, et al., J. Org. Chem. 89 (2024) 8111–8119.
doi: 10.1021/acs.joc.4c00771
Y. Xu, G. Zheng, L. Kong, X. Li, Org. Lett. 21 (2019) 3402–3406.
doi: 10.1021/acs.orglett.9b01139
A. Kong, X. Han, X. Lu, Org. Lett. 8 (2006) 1339–1342.
doi: 10.1021/ol060039u
X. Zhao, Z. Yu, T. Xu, P. Wu, H. Yu, Org. Lett. 9 (2007) 5263–5266.
doi: 10.1021/ol7024795
E.M. Ferreira, B.M. Stoltz, J. Am. Chem. Soc. 125 (2003) 9578–9579.
doi: 10.1021/ja035054y
A.C. Agy, M.T. Rodrigues Jr., L.A. Zeoly, D.A. Simoni, F. Coelho, J. Org. Chem. 84 (2019) 5564–5581.
doi: 10.1021/acs.joc.9b00505
Z. Yin, Y. Yu, H. Mei, J. Han, Green Chem. 23 (2021) 3256–3260.
doi: 10.1039/d1gc00609f
Y. Yu, A. Liu, J. He, et al., Chin. Chem. Lett. 33 (2022) 4886–4890.
doi: 10.1016/j.cclet.2022.03.038
J. He, A. Liu, Y. Yu, et al., J. Org. Chem. 88 (2023) 6962–6972.
doi: 10.1021/acs.joc.3c00267
H. Mei, Y. Yu, C. Wang, A. Liu, J. Han, Org. Chem. Front. 9 (2022) 2516–2521.
doi: 10.1039/d2qo00247g
H. Mei, A. Liu, J. He, Y. Yu, J. Han, Org. Lett. 24 (2022) 2630–2635.
doi: 10.1021/acs.orglett.2c00626
A. Liu, J. He, Y. Yu, et al., J. Org. Chem. 87 (2022) 11469–11477.
doi: 10.1021/acs.joc.2c01033
J. He Wang, H. Mei, J. Han, Tetrahedron Lett. 127 (2023) 154664.
doi: 10.1016/j.tetlet.2023.154664
X. Zhang, W.B. Liu, Q.F. Wu, S.L. You, Org. Lett. 15 (2013) 3746–3749.
doi: 10.1021/ol4016578
Q.F. Wu, H. He, W.B. Liu, S.L. You, J. Am. Chem. Soc. 132 (2010) 11418–11419.
doi: 10.1021/ja105111n
G. Han, Q. Wang, L. Chen, Y. Liu, Q. Wang, Adv. Synth. Catal. 358 (2016) 561–566.
doi: 10.1002/adsc.201500988
M. Zhu, K. Zhou, X. Zhang, S.L. You, Org. Lett. 20 (2018) 4379–4383.
doi: 10.1021/acs.orglett.8b01899
Y. Zhao, T. Hou, L. Zhang, et al., Eur. J. Org. Chem. 26 (2023) e202300253.
doi: 10.1002/ejoc.202300253
J. He, H. Mei, J. Escorihuela, J. Han, Chin. J. Chem. 42 (2024) 1691–1698.
doi: 10.1002/cjoc.202400127
J. He, C. Wang, H. Mei, A. Makarem, V.A. Soloshonok, J. Han, Tetrahedron 150 (2024) 133776.
doi: 10.1016/j.tet.2023.133776
D. Luo, Q. Wang, J. Liu, H. Mei, J. Han, Org. Biomol. Chem. 23 (2025) 1309–1313.
doi: 10.1039/d4ob01703j
D.Y. Yang, L. Liu, J.Y. Gu, Y.H. He, Z. Guan, J. Org. Chem. 86 (2021) 18042–18055.
doi: 10.1021/acs.joc.1c02335
J. Zhao, T. Wei, S. Ke, Y. Li, Chin. J. Org. Chem. 43 (2023) 1102–1114.
doi: 10.6023/cjoc202212032
E. Ascic, R.G. Ohm, R. Petersen, et al., Chem. Eur. J. 20 (2014) 3297–3300.
doi: 10.1002/chem.201304270
P.L. Zhu, Z. Zhang, X.Y. Tang, I. Marek, M. Shi, ChemCatChem 7 (2015) 595–600.
doi: 10.1002/cctc.201402940
T. Fan, H.H. Zhang, C. Li, Y. Shen, F. Shi, Adv. Synth. Catal. 358 (2016) 2017–2031.
doi: 10.1002/adsc.201501175
B. Alcaide, P. Almendros, I. Fernández, F. Herrera, A. Luna, Chem. Eur. J. 24 (2018) 1448–1454.
doi: 10.1002/chem.201705294
M.L. Bennasar, D. Solé, E. Zulaica, S. Alonso, Org. Lett. 13 (2011) 2042–2045.
doi: 10.1021/ol200437k
H.D. Zuo, X. Chen, Y.Y. Yuan, et al., Org. Lett. 26 (2024) 3810–3815.
doi: 10.1021/acs.orglett.4c00935
H.D. Zuo, X. Chen, Y. Zhang, et al., Org. Lett. 26 (2024) 3828–3833.
doi: 10.1021/acs.orglett.4c00981
Y.Y. Yuan, X. Chen, J.Y. Wang, et al., Eur. J. Org. Chem. 27 (2024) e202301256.
doi: 10.1002/ejoc.202301256
H.D. Zuo, Y.Y. Yuan, X. Chen, et al., Adv. Synth. Catal. 366 (2024) 3578–3584.
doi: 10.1002/adsc.202400475
T. Xia, R. Yu, J. Chen, et al., Org. Lett. 27 (2025) 6415–6421.
doi: 10.1021/acs.orglett.5c01722
L. Li, X.Q. Zhu, Y.Q. Zhang, et al., Chem. Sci. 10 (2019) 3123–3129.
doi: 10.1039/C9SC00079H
S.J. Gharpure, S. Kumari, Chem. Commun. 60 (2024) 538–541.
doi: 10.1039/d3cc05237k
C.R. Reddy, P. Sathish, K. Mallesh, Y.L. Prapurna, ChemistrySelect 5 (2020) 12736–12739.
doi: 10.1002/slct.202002689
P. Sathish, M. Subbarao, Y.L. Prapurna, Chem. Data Collect. 39 (2022) 100865.
doi: 10.1016/j.cdc.2022.100865
X. Zou, Y.T. Wang, P.C. Xu, et al., J. Org. Chem. 90 (2025) 15804–15818.
doi: 10.1021/acs.joc.5c02081
P. Singh, M.V. Mane, S.K. Mahto, A.C. Shaikh, Org. Lett. 27 (2025) 8217–8222.
doi: 10.1021/acs.orglett.5c02333
H. Liao, J. Yang, Chen, et al., J. Org. Chem. 90 (2025) 16193–16199.
doi: 10.1021/acs.joc.5c02230
Y. Liu, L. Bao, X. Lyu, et al., Chin. Chem. Lett. 36 (2025) 112201.
C. Sun, Y. Bu, J. Chen, et al., Eur. J. Org. Chem. 28 (2025) e202500602.
doi: 10.1002/ejoc.202500602
S.J. Gharpure, R.S. Chavan, K.C. Pansuriya, A. Khandelwal, Org. Lett. 27 (2025) 14017–14022.
doi: 10.1021/acs.orglett.5c04595
Xuling Pan , Wei Cai , You Huang . Recent advances in phosphine-mediated sequential annulations. Chinese Chemical Letters, 2025, 36(5): 110628-. doi: 10.1016/j.cclet.2024.110628
Huili Zhao , Xiao Tan , Huining Chai , Lin Hu , Hongbo Li , Lijun Qu , Xueji Zhang , Guangyao Zhang . Recent advances in conductive MOF-based electrochemical sensors. Chinese Chemical Letters, 2025, 36(8): 110571-. doi: 10.1016/j.cclet.2024.110571
Fangxiang SUN , Qing ZHANG , Yifan ZHANG , Haoyi SUN , Akim V. Shmal′ko , Sergey A. Anufriev , Igor B. Sivaev , Deshuang TU , Hong YAN . Pd-catalyzed B—H bond activation and annulation of nido-carborane with terminal olefins: Facile construction of 2D-3D fused polycyclic compounds. Chinese Journal of Inorganic Chemistry, 2026, 42(3): 467-478. doi: 10.11862/CJIC.20250347
Junhua Li , Yu Fu , Yian Shi . A rapid access to fused polycyclic indolo[2,1-a]isoquinolins via Pd-catalyzed sequential Heck/C-H activation/amination reaction with diaziridinone. Chinese Chemical Letters, 2026, 37(3): 111376-. doi: 10.1016/j.cclet.2025.111376
Yi-Fan Wang , Hao-Yun Yu , Hao Xu , Ya-Jie Wang , Xiaodi Yang , Yu-Hui Wang , Ping Tian , Guo-Qiang Lin . Rhodium(Ⅲ)-catalyzed diastereo- and enantioselective hydrosilylation/cyclization reaction of cyclohexadienone-tethered α, β-unsaturated aldehydes. Chinese Chemical Letters, 2024, 35(9): 109520-. doi: 10.1016/j.cclet.2024.109520
Lei Li , Xin-Ying Zhu , Jun-Yu Zhu , Zhi-Hao Wu , Yan-Jiang Zhang , Fang-Yu Yuan , Dong Huang , Sheng Yin , Gui-Hua Tang . Penispirolactam and penipyrroloindole, two unusual polycyclic indole diterpenoids with anti-hepatic fibrosis activity from the endophytic fungus Penicillium janthinellum H-6. Chinese Chemical Letters, 2026, 37(4): 111161-. doi: 10.1016/j.cclet.2025.111161
Yinuo Wang , Ziyu Liu , Hongxia Tan , Jun Tong , Dazhen Xu . Synthesis of Bromobenzoxazine: Introduce a Comprehensive Organic Chemistry Experiment Transformed from Undergraduate Research Innovation. University Chemistry, 2025, 40(10): 208-216. doi: 10.12461/PKU.DXHX202411077
Jingyuan Yang , Xinyu Tian , Liuzhong Yuan , Yu Liu , Yue Wang , Chuandong Dou . Enhancing stability of diradical polycyclic hydrocarbons via P=O-attaching. Chinese Chemical Letters, 2024, 35(8): 109745-. doi: 10.1016/j.cclet.2024.109745
Rita Favas , Marta Monteiro , Hugo Almeida , Domingos Ferreira , Andreia Filipa Peixoto , Ana Catarina Silva . Marine bioactive compounds: Sustainable sources, green extraction, and healthcare applications. Chinese Chemical Letters, 2026, 37(6): 111482-. doi: 10.1016/j.cclet.2025.111482
Kebo Xie , Qian Zhang , Fei Ye , Jungui Dai . A multi-enzymatic cascade reaction for the synthesis of bioactive C-oligosaccharides. Chinese Chemical Letters, 2024, 35(6): 109028-. doi: 10.1016/j.cclet.2023.109028
Zhengyi Shi , Jie Yin , Yang Xiao , Zhangrong Hou , Fei Song , Jianping Wang , Qingyi Tong , Changxing Qi , Yonghui Zhang . Unprecedented sesquiterpene-polycyclic polyprenylated acylphloroglucinol adduct against acute myeloid leukemia via inhibiting mitochondrial complex Ⅴ. Chinese Chemical Letters, 2024, 35(10): 109458-. doi: 10.1016/j.cclet.2023.109458
Chunmao Yuan , Yanrong Zeng , Lei Huang , Yu Mou , Jun Jin , Ping Yi , Yanmei Li , Xiaojiang Hao . Hymoins A–C, three unusual polycyclic polyprenylated acylphloroglucinols with lipid-lowering activity from Hypericum monogynum. Chinese Chemical Letters, 2025, 36(3): 109859-. doi: 10.1016/j.cclet.2024.109859
Xianxu Chu , Lu Wang , Junru Li , Hui Xu . Surface chemical microenvironment engineering of catalysts by organic molecules for boosting electrocatalytic reaction. Chinese Chemical Letters, 2024, 35(8): 109105-. doi: 10.1016/j.cclet.2023.109105
Guru Prasanna Sahoo , Tushar Kanti Rajwar , Jitu Halder , Ajit Mishra , Ritu Mahanty , Ivy Saha , Bibhanwita Satpathy , Rakesh Kumar Sahoo , Deepak Pradhan , Vineet Kumar Rai , Priyanka Dash , Chandan Das , Manoj Kumar Sarangi , Saroj Kumar Rout , Biswakanth Kar , Goutam Ghosh , Goutam Rath . Natural bioactive compounds loaded chitosan nanocarriers: A promising strategy for breast cancer therapy. Chinese Chemical Letters, 2026, 37(8): 111797-. doi: 10.1016/j.cclet.2025.111797
Tingting Huang , Zhuanlong Ding , Hao Liu , Ping-An Chen , Longfeng Zhao , Yuanyuan Hu , Yifan Yao , Kun Yang , Zebing Zeng . Electron-transporting boron-doped polycyclic aromatic hydrocarbons: Facile synthesis and heteroatom doping positions-modulated optoelectronic properties. Chinese Chemical Letters, 2024, 35(4): 109117-. doi: 10.1016/j.cclet.2023.109117
Wu-Yang Liu , Xin-Xiang Lei , Wen-Ji Wang , Jun-Mian Tian , Yu-Qi Gao , Jin-Ming Gao . Hyperforatone A, the 1,8-seco rearranged polycyclic polyprenylated acylphloroglucinol with a unique bicyclo[5.4.0]undecane core from Hypericum perforatum. Chinese Chemical Letters, 2025, 36(4): 110478-. doi: 10.1016/j.cclet.2024.110478
Haifeng ZHENG , Xingzhe GUO , Yunwei WEI , Xinfang WANG , Huimin QI , Yuting YAN , Jie ZHANG , Bingwen LI . Post-synthetic modification strategy to construct Co-MOF composites for boosting oxygen evolution reaction activity. Chinese Journal of Inorganic Chemistry, 2026, 42(1): 193-202. doi: 10.11862/CJIC.20250029
Zixuan Zhu , Xianjin Shi , Yongfang Rao , Yu Huang . Recent progress of MgO-based materials in CO2 adsorption and conversion: Modification methods, reaction condition, and CO2 hydrogenation. Chinese Chemical Letters, 2024, 35(5): 108954-. doi: 10.1016/j.cclet.2023.108954
Yaping Zhang , Wei Zhou , Mingchun Gao , Tianqi Liu , Bingxin Liu , Chang-Hua Ding , Bin Xu . Oxidative cyclization of allyl compounds and isocyanide: A facile entry to polysubstituted 2-cyanopyrroles. Chinese Chemical Letters, 2024, 35(4): 108836-. doi: 10.1016/j.cclet.2023.108836
Yi-Kao Xu , Guo-Ping Luo , Liang-Bin Hu , Wei-Min He . Asymmetric Büchner reaction and arene cyclopropanation via copper-catalyzed controllable cyclization of diynes. Chinese Chemical Letters, 2025, 36(8): 111226-. doi: 10.1016/j.cclet.2025.111226