Citation: Wang Yuying, Liu Li, Wang Yeming. Advances Research in Synthesis of Aza-heterocyclic Compounds Involving Vinyl Azides[J]. Chinese Journal of Organic Chemistry, ;2018, 38(5): 1009-1028. doi: 10.6023/cjoc201711043 shu

Advances Research in Synthesis of Aza-heterocyclic Compounds Involving Vinyl Azides

Wang Yuying ^a ,
Liu Li ^a,, ,
Wang Yeming ^b,,

a.
College of Pharmaceutical Sciences, Changchun University of Chinese Medicine, Changchun 130117
b.
College of Chemistry, Jilin Normal University, Siping 136000

Corresponding author: Liu Li, 68734263@qq.com Wang Yeming, wangyeming2011@163.com
Received Date: 23 November 2017
Revised Date: 30 December 2017
Available Online: 10 May 2018

Figures(43)

Vinyl azides have been extensively studied in organic synthesis since 1910. As a series of important intermediates, vinyl azides have a wide range of applications in recent years, especially in the synthesis of heterocyclic compounds catalyzed by transition-metals. The progress of the construction of aza-heterocyclic compounds in the field of organic synthesis is reviewed.
- vinyl azide,
- synthesis,
- aza-heterocycle
1. [1]
  Forster, M. O.; Newman, S. H. J. Chem. Soc. 1910, 97, 2570. doi: 10.1039/CT9109702570
2. [2]
  Hemetsberger, H.; Knittel, D.; Weidmann, H. Monatsh. Chem. 1969, 100, 1599. doi: 10.1007/BF00900176
3. [3]
  Zhu, W.; Ma, D.-W. Chem. Commun. 2004, 888.
4. [4]
  Hassner, A.; Levy, L. A. J. Am. Chem. Soc. 1965, 87, 4203. doi: 10.1021/ja01096a045
5. [5]
  Harvey, G. R.; Ratts, K. W. J. Org. Chem. 1966, 31, 3907. doi: 10.1021/jo01350a005
6. [6]
  Priebe, H. Angew. Chem., Int. Ed. Engl. 1984, 23, 736. doi: 10.1002/(ISSN)1521-3773
7. [7]
  Chou, T. S.; Lee, S. J.; Peng, M. L.; Sun D. J.; Chou, S. S. P. J. Org. Chem. 1988, 53, 3027. doi: 10.1021/jo00248a023
8. [8]
  Fu, J.-K.; Giuseppe, Z.; Edward, A. A.; Bi, X.-H. Chem. Soc. Rev. 2017, 46, 7208. doi: 10.1039/C7CS00017K
9. [9]
  Zhang, L.; Sun, G.; Bi, X.-H. Chem.-Asian J. 2016, 11, 3018. doi: 10.1002/asia.v11.21
10. [10]
  Yan, J.; Ji, X.-Y.; Hua, S.-G.; Wang, J. Chin. J. Org. Chem. 2018, 38, 791(in Chinese).
11. [11]
  (a) Neber, P. W. ; Burgard, A. Justus Liebigs Ann. Chem. 1932, 493, 281.
  (b) Neber, P. W. ; Huh, G. Justus Liebigs Ann. Chem. 1935, 515, 283.
12. [12]
  (a) Würthwein, T. ; Hergenrö ther, T. ; Quast, H. Eur. J. Org. Chem. 2002, 1750.
  (b) Banert, K. ; Meier, B. Angew. Chem., Int. Ed. 2006, 45, 4015.
13. [13]
  (a) Smolinsky, G. J. Am. Chem. Soc. 1961, 83, 4483.
  (b) Smolinsky, G. J. Org. Chem. 1962, 27, 3557.
14. [14]
  Alves, M. J.; Bickley, J. F.; Gilchrist, T. L. J. Chem. Soc., Perkin Trans. 1 1999, 1399.
15. [15]
  Patonay, T.; Jeko, J.; Juhasz-Toth, E. Eur. J. Org. Chem. 2008, 1441.
16. [16]
  Kumar, R.; Nath, M.; Tyrrell, D. L. J. J. Med. Chem. 2002, 45, 2032. doi: 10.1021/jm010410d
17. [17]
  Pinhoe Melo, T. M. V. D.; Lopes, C. S. J.; Cardoso, A. L.; Rocha Gonsalves, A. M. d'A. Tetrahedron 2001, 57, 6203. doi: 10.1016/S0040-4020(01)00598-1
18. [18]
  Alonso-Cruz, C. R.; Kennedy, A. R.; Rodríguez, M. S.; Suárez, E. Tetrahedron Lett. 2007, 48, 7207. doi: 10.1016/j.tetlet.2007.07.190
19. [19]
  Alonso-Cruz, C. R.; Kennedy, A. R.; Rodríguez, M. S.; Suárez, E. J. Org. Chem. 2008, 73, 4116. doi: 10.1021/jo800182y
20. [20]
  Timen, A. S.; Risberg, E.; Somfai, P. Tetrahedron Lett. 2003, 44, 5339. doi: 10.1016/S0040-4039(03)01205-X
21. [21]
  Alajarín, M.; Orenes, R.; Vidal, Á.; Pastor, A. Synthesis 2003, 49.
22. [22]
  Singh, P. N. D.; Carter, C. L.; Gudmundsdóttir, A. D. Tetrahedron Lett. 2003, 44, 6763. doi: 10.1016/S0040-4039(03)01558-2
23. [23]
  Furin, G. G.; Gatilov, Y. V.; Bagrynskay, I. Y.; Zhuzhgov, E. L. J. Fluorine Chem. 2001, 110, 21. doi: 10.1016/S0022-1139(01)00395-5
24. [24]
  Banert, K.; Kohler, F.; Kowski, K.; Meier, B.; Muller, B.; Rademacher, P. Chem.-Eur. J. 2002, 8, 5089. doi: 10.1002/1521-3765(20021115)8:22<5089::AID-CHEM5089>3.0.CO;2-F
25. [25]
  Banert, K.; Fotsing, J. R.; Hagedorn, M.; Reisenauer, H. P.; Maier, G. Tetrahedron 2008, 64, 5645. doi: 10.1016/j.tet.2008.04.037
26. [26]
  Banert, K.; Hagedorn, M.; Wutke, J.; Ecorchard, P.; Schaarschmidt, D.; Lang, H. Chem. Commun. 2010, 46, 4058. doi: 10.1039/c0cc00079e
27. [27]
  Banert, K.; Kçhler, F.; Melzer, A.; Scharf, I.; Rheinwald, G.; Ruffer, T.; Lang, H.; Herges, R.; He , K.; Ghavtadze, N.; Wurthwein, E.-U. Chem.-Eur. J. 2011, 17, 10071. doi: 10.1002/chem.v17.36
28. [28]
  Banert, K.; Meier, B.; Penk, E.; Saha, B.; Wurthwein, E.-U.; Grimme, S.; Ruffer, T.; Schaarschmidt, D.; Lang, H. Chem.-Eur. J. 2011, 17, 1128. doi: 10.1002/chem.v17.4
29. [29]
  Banert, K.; Ihle, A.; Kuhtz, A.; Penk, E.; Saha, B.; Würthwein, E.-U. Tetrahedron 2013, 69, 2501. doi: 10.1016/j.tet.2012.12.054
30. [30]
  Chen, F.; Shen, T.; Cui, Y.-X.; Jiao, N. Org. Lett. 2012, 14, 4926. doi: 10.1021/ol302270z
31. [31]
  Donthiri, R. R.; Samanta, S.; Adimurthy, S. Org. Biomol. Chem. 2015, 13, 10113. doi: 10.1039/C5OB01407G
32. [32]
  Chiba, S.; Wang, Y.-F.; Lapointe, G.; Narasaka, K. Org. Lett. 2008, 10, 313. doi: 10.1021/ol702727j
33. [33]
  Ng, E. P. J.; Wang, Y.-F.; Hui, B. W.-Q.; Lapointe, G.; Chiba, S. Tetrahedron 2011, 67, 7728. doi: 10.1016/j.tet.2011.08.006
34. [34]
  Wang, Y.-F.; Toh, K. K.; Chiba, S.; Narasaka, K. Org. Lett. 2008, 10, 5019. doi: 10.1021/ol802120u
35. [35]
  Ng, E. P. J.; Wang, Y.-F.; Chiba, S. Synlett 2011, 783.
36. [36]
  Yu, W.-W.; Chen, W.-T.; Liu, S.; Shao, J.-A.; Shao, Z.-Y.; Lin, H.-L.; Yu, Y.-P. Tetrahedron 2013, 69, 1953. doi: 10.1016/j.tet.2012.11.041
37. [37]
  Chen, W.-T.; Shao, J.-A.; Li, Z.; Giulianotti, M. A.; Yu, Y.-P. Can. J. Chem. 2012, 90, 214. doi: 10.1139/v11-150
38. [38]
  Wu, Y.-F.; Zhu, L.; Yu, Y.-H.; Luo, X.-S.; Huang, X.-L. J. Org. Chem. 2015, 80, 11407. doi: 10.1021/acs.joc.5b02057
39. [39]
  Pawar, S. K.; Sahani, R. L.; Liu, R.-S. Chem.-Eur. J. 2015, 21, 10843. doi: 10.1002/chem.v21.30
40. [40]
  Zhu, L.; Yu, Y.-H.; Mao, Z.-F.; Huang, X.-L. Org. Lett. 2015, 17, 30. doi: 10.1021/ol503172h
41. [41]
  Cludius-Brandt, S.; Kupracz, L.; Kirschning, A. Beilstein J. Org. Chem. 2013, 9, 1745. doi: 10.3762/bjoc.9.201
42. [42]
  Dong, H.-J.; Shen, M.-H.; Redford, J. E.; Stokes, B. J.; Pumphrey, A. L.; Driver, T. G. Org. Lett. 2007, 9, 5191. doi: 10.1021/ol702262f
43. [43]
  Farney, E. P.; Yoon, T. P. Angew. Chem., Int. Ed. 2014, 53, 793. doi: 10.1002/anie.201308820
44. [44]
  Zhang, L.; Sun, G.; Bi, X.-H. Chem.-Asian J. 2016, 11, 3018. doi: 10.1002/asia.v11.21
45. [45]
  Nie, Y.-B.; Wang, L.; Ding, M.-W. J. Org. Chem. 2012, 77, 696. doi: 10.1021/jo201846w
46. [46]
  Wang, Y.; Xie, H.; Pan, Y.-R.; Ding, M. W. Synthesis 2014, 336.
47. [47]
  Liu, S.; Shao, J.-A.; Guo, X.; Luo, J.; Zhao, M.-H.; Zhang, G.-L.; Yu, Y.-P. Tetrahedron 2014, 70, 1418. doi: 10.1016/j.tet.2014.01.007
48. [48]
  Luo, J.; Chen, W.-T.; Shao, J.-A.; Liu, X.-Y.; Shu, K.; Tang, P.; Yu, Y.-P. RSC Adv. 2015, 5, 55808. doi: 10.1039/C5RA07320K
49. [49]
  Xiang, L.-K.; Niu, Y.-N.; Pang, X.-B.; Yang, X.-D.; Yan, R.-L. Chem. Commun. 2015, 51, 6598. doi: 10.1039/C5CC01155H
50. [50]
  Tiwari, D. K.; Maurya, R. A.; Nanubolu, J. B. Chem.-Eur. J. 2016, 22, 526. doi: 10.1002/chem.201504292
51. [51]
  Adiyala, P. R.; Borra, S.; Kamal, A.; Maurya, R. A. Eur. J. Org. Chem. 2016, 1269.
52. [52]
  Zhu, Z.-Z.; Tang, X.-D.; Li, J.-X.; Li, X.-W.; Wu, W.-Q.; Deng, G.-H.; Jiang, H.-F. Org. Lett. 2017, 19, 1370. doi: 10.1021/acs.orglett.7b00203
53. [53]
  Hu, J.-T.; Cheng, Y.-F.; Yang, Y.-Q.; Rao, Y. Chem. Commun. 2011, 47, 10133. doi: 10.1039/c1cc13908h
54. [54]
  (a) Zou, H. -B. ; Zhu, H. -J. ; Shao, J. -A. ; Wu, J. -W. ; Chen, W. -T. ; Giulianotti, M. A. ; Yu, Y. -P. Tetrahedron 2011, 67, 4887.
  (b) Li, Y. ; Hong, D. ; Lu, P. ; Wang, Y. G. Tetrahedron Lett. 2011, 52, 4161.
55. [55]
  Zhang, G.-L.; Ni, H.-C.; Chen, W.-T.; Shao, J.-A.; Liu, H.; Chen, B.-H.; Yu, Y.-P. Org. Lett. 2013, 15, 5967. doi: 10.1021/ol402810f
56. [56]
  Huang, W.; Liu, S.; Chen, B.-H.; Guo, X.; Yu, Y.-P. RSC Adv. 2015, 5, 32740. doi: 10.1039/C5RA04371A
57. [57]
  (a) Wang Y. -F. ; Chiba, S. J. Am. Chem. Soc. 2009, 131, 12570.
  (b) Wang, Y. F. ; Toh, K. K. ; Ng, E. P. J. ; Chiba, S. J. Am. Chem. Soc. 2011, 133, 6411.
58. [58]
  Sajna, K. V.; Kumara Swamy, K. C. J. Org. Chem. 2012, 77, 8712. doi: 10.1021/jo301694n
59. [59]
  Shao, Z.-Y.; Pan, Q.-H.; Chen, J.; Yu, Y.-P.; Zhang, G.-L. Tetrahedron 2012, 68, 6565. doi: 10.1016/j.tet.2012.05.057
60. [60]
  Nishimura, Y.; Hidetsura, C. H. Synlett 2015, 233.
61. [61]
  Shao, J.-A.; Liu, X.-Y.; Shu, K.; Tang, P.; Luo, J.; Chen, W.-T.; Yu, Y.-P. Org. Lett. 2015, 17, 4502. doi: 10.1021/acs.orglett.5b02180
62. [62]
  Knittel, D. Synthesis 1985, 186.
63. [63]
  Stokes, B. J.; Dong, H.; Leslie, B. E.; Pum-phrey, A. L.; Driver, T. G. J. Am. Chem. Soc. 2007, 129, 7500. doi: 10.1021/ja072219k
64. [64]
  Hong, D.; Chen, Z.-B.; Lin, X.-F.; Wang, Y.-G. Org. Lett. 2010, 12, 4608. doi: 10.1021/ol101934v
65. [65]
  Zhu, X.; Wang, Y.-F.; Zhang, F.-L.; Chiba, S. Chem.-Asian J. 2014, 9, 2458. doi: 10.1002/asia.201402421
66. [66]
  Wang, Q.-L.; Huang, J.; Zhou, L. Adv. Synth. Catal. 2015, 357, 2479. doi: 10.1002/adsc.v357.11
67. [67]
  (a) Yang, Y. Y. ; Shou, W. G. ; Chen, Z. B. ; Hong, D. J. Org. Chem. 2008, 73, 3928.
  (b) Chen, Z. B. ; Hong, D. ; Wang, Y. -G. J. Org. Chem. 2009, 74, 903.
68. [68]
  Wang, Y.-F.; Toh, K.-K.; Lee, J.-Y.; Chiba, S. Angew. Chem., Int. Ed. 2011, 50, 5927. doi: 10.1002/anie.v50.26
69. [69]
  Wang, Y.-F.; Lonca, G. H.; Chiba, S. Angew. Chem., Int. Ed. 2014, 53, 1067. doi: 10.1002/anie.201307846
70. [70]
  Liu, K.; Chen, S.; Li, X.-G.; Liu, P.-N. J. Org. Chem. 2016, 81, 265. doi: 10.1021/acs.joc.5b01995
71. [71]
  Zhu, Z.-Z.; Tang, X.-D.; Li, X.-W.; Wu, W.-Q.; Deng, G.-H.; Jiang, H.-F. J. Org. Chem. 2016, 81, 1401. doi: 10.1021/acs.joc.5b02376
72. [72]
  Wang, Y. F.; Lonca, G. H.; Runigo, M. L.; Chiba, S. Org. Lett. 2014, 16, 4272. doi: 10.1021/ol501997n
73. [73]
  Mackay, E. G.; Studer, A. Chem.-Eur. J. 2016, 22, 13455. doi: 10.1002/chem.201602855
74. [74]
  Sun, X.-Y.; Yu, S.-Y. Chem. Commun. 2016, 52, 10898. doi: 10.1039/C6CC05756J
75. [75]
  Chen, W.-T.; Hu, M.; Wu, J.-W.; Zou, H.-B.; Yu, Y.-P. Org. Lett. 2010, 12, 3863. doi: 10.1021/ol101538x
76. [76]
  Donthiri, R. R.; Pappula, V.; Reddy, N. N. K.; Bairagi, D.; Adimurthy, S. J. Org. Chem. 2014, 79, 11277. doi: 10.1021/jo5021618
77. [77]
  Adiyala, P. R.; Mani, G. S.; Nanubolu, J. B.; Shekar, K. C.; Maurya, R. A. Org. Lett. 2015, 17, 4308. doi: 10.1021/acs.orglett.5b02124
78. [78]
  Dinda, B. K.; Jana, A. K.; Mal, D. Chem. Commun. 2012, 48, 3999. doi: 10.1039/c2cc30279a
79. [79]
  Guo, S.-S.; Chen, B.-H.; Guo, X.; Zhang, G.-L.; Yu, Y.-P. Tetrahedron 2015, 71, 9371. doi: 10.1016/j.tet.2015.08.067
80. [80]
  Guo, S.-S.; Chen, B.-H.; Zhao, D.-H.; Chen, W.-T.; Zhang, G.-L. Adv. Synth. Catal. 2016, 358, 3010. doi: 10.1002/adsc.v358.19
81. [81]
  Xu, H.-D.; Zhou, H.; Pan, Y.-P.; Ren, X.-T.; Wu, H.; Han, M.; Han, R.-Z.; Shen, M.-H. Angew. Chem., Int. Ed. 2016, 55, 2540. doi: 10.1002/anie.201510096
1. [1]
  Lixing ZHANG , Yaowen WANG , Xu HAN , Junhong ZHOU , Jinghui WANG , Liping LI , Guangshe LI . Research progress in the synthesis of fluorine-containing perovskites and their derivatives. Chinese Journal of Inorganic Chemistry, 2025, 41(9): 1689-1701. doi: 10.11862/CJIC.20250007
2. [2]
  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
3. [3]
  Lifang HE , Wenjie TANG , Yaoze LUO , Mingsheng LIANG , Jianxin TANG , Yuxuan WU , Fuxing ZHANG , Xiaoming ZHU . Synthesis, structure, and anticancer activity of two dialkyltin complexes constructed based on 2, 2′-bipyridin-6, 6′-dicarboxylic acid. Chinese Journal of Inorganic Chemistry, 2025, 41(8): 1601-1609. doi: 10.11862/CJIC.20250012
4. [4]
  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
5. [5]
  Ying Chen , Ronghua Yan , Weiyan Yin . Research Progress on the Synthesis of Metal Single-Atom Catalysts and Their Applications in Electrocatalytic Hydrogen Evolution Reactions. University Chemistry, 2025, 40(9): 344-353. doi: 10.12461/PKU.DXHX202503066
6. [6]
  Bin SUN , Heyan JIANG . Glucose-modified bis-Schiff bases: Synthesis and bio-activities in Alzheimer′s disease therapy. Chinese Journal of Inorganic Chemistry, 2025, 41(7): 1338-1350. doi: 10.11862/CJIC.20240428
7. [7]
  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
8. [8]
  Xinyi Zhang , Kai Ren , Yanning Liu , Zhenyi Gu , Zhixiong Huang , Shuohang Zheng , Xiaotong Wang , Jinzhi Guo , Igor V. Zatovsky , Junming Cao , Xinglong Wu . Progress on Entropy Production Engineering for Electrochemical Catalysis. Acta Physico-Chimica Sinica, 2024, 40(7): 2307057-0. doi: 10.3866/PKU.WHXB202307057
9. [9]
  Lei Feng , Ze-Min Zhu , Ying Yang , Zongbin He , Jiafeng Zou , Man-Bo Li , Yan Zhao , Zhikun Wu . Long-Pursued Structure of Au₂₃(S-Adm)₁₆ and the Unexpected Doping Effects. Acta Physico-Chimica Sinica, 2024, 40(5): 2305029-0. doi: 10.3866/PKU.WHXB202305029
10. [10]
  Chunling Qin , Shuang Chen , Hassanien Gomaa , Mohamed A. Shenashen , Sherif A. El-Safty , Qian Liu , Cuihua An , Xijun Liu , Qibo Deng , Ning Hu . Regulating HER and OER Performances of 2D Materials by the External Physical Fields. Acta Physico-Chimica Sinica, 2024, 40(9): 2307059-0. doi: 10.3866/PKU.WHXB202307059
11. [11]
  Chi Li , Jichao Wan , Qiyu Long , Hui Lv , Ying Xiong . N-Heterocyclic Carbene (NHC)-Catalyzed Amidation of Aldehydes with Nitroso Compounds. University Chemistry, 2024, 39(5): 388-395. doi: 10.3866/PKU.DXHX202312016
12. [12]
  Fei Liu , Dong-Yang Zhao , Kai Sun , Ting-Ting Yu , Xin Wang . Comprehensive Experimental Design for Photochemical Synthesis, Analysis, and Characterization of Seleno-Containing Medium-Sized N-Heterocycles. University Chemistry, 2024, 39(3): 369-375. doi: 10.3866/PKU.DXHX202309047
13. [13]
  Xiao SANG , Qi LIU , Jianping LANG . Synthesis, structure, and fluorescence properties of Zn(Ⅱ) coordination polymers containing tetra-alkenylpyridine ligands. Chinese Journal of Inorganic Chemistry, 2024, 40(11): 2124-2132. doi: 10.11862/CJIC.20240158
14. [14]
  Hong RAO , Yang HU , Yicong MA , Chunxin LÜ , Wei ZHONG , Lihua DU . Synthesis and in vitro anticancer activity of phenanthroline-functionalized nitrogen heterocyclic carbene homo- and heterobimetallic silver/gold complexes. Chinese Journal of Inorganic Chemistry, 2024, 40(12): 2429-2437. doi: 10.11862/CJIC.20240275
15. [15]
  Mengyang LI , Hao XU , Zhonghao NIU , Chunhua GONG , Weihui ZHONG , Jingli XIE . Highly effective catalytic synthesis of β-amino alcohols by using viologen-polyoxometalate hybrid materials. Chinese Journal of Inorganic Chemistry, 2025, 41(7): 1294-1300. doi: 10.11862/CJIC.20250080
16. [16]
  Liping GUO . Synthesis and crystal structure characterization of yttrium imido complex: The reactivity of 2-substituted-1-amino-o-carborane with yttrium dialkyl complex. Chinese Journal of Inorganic Chemistry, 2025, 41(7): 1409-1415. doi: 10.11862/CJIC.20250065
17. [17]
  Rui Gao , Ying Zhou , Yifan Hu , Siyuan Chen , Shouhong Xu , Qianfu Luo , Wenqing Zhang . Design, Synthesis and Performance Experiment of Novel Photoswitchable Hybrid Tetraarylethenes. University Chemistry, 2024, 39(5): 125-133. doi: 10.3866/PKU.DXHX202310050
18. [18]
  Yuhao SUN , Qingzhe DONG , Lei ZHAO , Xiaodan JIANG , Hailing GUO , Xianglong MENG , Yongmei GUO . Synthesis and antibacterial properties of silver-loaded sod-based zeolite. Chinese Journal of Inorganic Chemistry, 2024, 40(4): 761-770. doi: 10.11862/CJIC.20230169
19. [19]
  Minghui Wu , Markus Mühlinghaus , Xuechao Li , Chaojie Xu , Qiang Chen , Haiming Zhang , Klaus Müllen , Lifeng Chi . On-Surface Synthesis of Chevron-Shaped Conjugated Ladder Polymers Consisting of Benzo[a]azulene Units. Acta Physico-Chimica Sinica, 2024, 40(8): 2307024-0. doi: 10.3866/PKU.WHXB202307024
20. [20]
  Ruilan Fan , Xiaoling Huang . 磷源的选择及三种含磷阻燃剂的合成与阻燃性. University Chemistry, 2025, 40(8): 181-191. doi: 10.12461/PKU.DXHX202410025

Get Citation

PDF

XML

Metrics

PDF Downloads(96)
Abstract views(8943)
HTML views(2714)

通讯作者: 陈斌, bchen63@163.com

1.
沈阳化工大学材料科学与工程学院沈阳 110142