Chinese Journal of Organic Chemistry ›› 2020, Vol. 40 ›› Issue (12): 4168-4183.DOI: 10.6023/cjoc202005074 Previous Articles Next Articles
杨凯a,b, 姚辰b, 高娟娟c, 陈思鸿b, 郑雪洁b, 邓璐璇b, 张毓娜b, 刘美娟b, 汪朝阳b
收稿日期:
2020-05-27
修回日期:
2020-06-15
发布日期:
2020-07-01
通讯作者:
汪朝阳, 杨凯
E-mail:wangzy@scnu.edu.cn;kai_yangyang@126.com
基金资助:
Yang Kaia,b, Yao Chenb, Gao Juanjuanc, Chen Sihongb, Zheng Xuejieb, Deng Luxuanb, Zhang Yu'nab, Liu Meijuanb, Wang Zhaoyangb
Received:
2020-05-27
Revised:
2020-06-15
Published:
2020-07-01
Supported by:
Share
Yang Kai, Yao Chen, Gao Juanjuan, Chen Sihong, Zheng Xuejie, Deng Luxuan, Zhang Yu'na, Liu Meijuan, Wang Zhaoyang. Progress on the Synthesis of Pyrido[1,2-a]benzimidazoles[J]. Chinese Journal of Organic Chemistry, 2020, 40(12): 4168-4183.
[1] Stepien, M.; Gonka, E.; Zyla, M.; Sprutta, N. Chem. Rev. 2017, 117, 3479. [2] Tan, J.-F.; Bormann, C. T.; Perrin, F. G.; Chadwick, F. M.; Seyerin, K.; Cramer, N. J. Am. Chem. Soc. 2019, 141, 10372. [3] Gomha, S. M.; Eldebss, T. M. A.; Badrey, M. G.; Abdulla, M. M.; Mayhoub, A. S. Chem. Biol. Drug Des. 2015, 86, 1292. [4] Xie, Y.-J.; Wu, J.; Che, X.-Z.; Chen, Y.; Huang, H.-W.; Deng, G.-J. Green Chem. 2016, 18, 667. [5] Perin, N.; Bobanovic, K.; Zlatar, I.; Jelic, D.; Kelava, V.; Kostrun, S.; Markovic, V. G.; Brajsa, K.; Hranjec, M. Eur. J. Med. Chem. 2017, 125, 722. [6] Jovanovic, I. N.; Jadresko, D.; Milicevic, A.; Hranjec, M.; Perin, N. Electrochim. Acta 2019, 297, 452. [7] Okombo, J.; Brunschwig, C.; Singh, K.; Dziwornu, G. A.; Barnard, L.; Njoroge, M.; Wittlin, S.; Chibale, K. ACS Infect. Dis. 2019, 5, 372. [8] Mayoka, G.; Njoroge, M.; Okombo, J.; Gibhard, L.; Sanches-Vaz, M.; Fontinha, D.; Birkholtz, L. M.; Reader, J.; van der Watt, M.; Coetzer, T. L.; Lauterbach, S.; Churchyard, A.; Bezuidenhout, B.; Egan, T. J.; Yeates, C.; Wittlin, S.; Prudencio, M.; Chibale, K. J. Med. Chem. 2019, 62, 1022. [9] Takeshita, H.; Watanabe, J.; Kimura, Y.; Kawakami, K.; Takahashi, H.; Takemura, M.; Kitamura, A.; Someya, K.; Nakajima, R. Bioorg. Med. Chem. Lett. 2010, 20, 3893. [10] Okombo, J.; Singh, K.; Mayoka, G.; Ndubi, F.; Barnard, L.; Njogu, P. M.; Njoroge, M.; Gibhard, L.; Brunschwig, C.; Vargas, M.; Keiser, J.; Egan, T. J.; Chibale, K. ACS Infect. Dis. 2017, 3, 411. [11] Chalmers, B. A.; Saha, S.; Nguyen, T.; McMurtrie, J.; Sigurdsson, S. T.; Bottle, S. E.; Masters, K. S. Org. Lett. 2014, 16, 5528. [12] Karak, P.; Dutta, C.; Dutta, T.; Koner, A. L.; Choudhury, J. Chem. Commun. 2019, 55, 6791. [13] Pericherla, K.; Kaswan, P.; Pandey, K.; Kumar, A. Synthesis 2015, 47, 887. [14] Bagdi, A. K.; Santra, S.; Monir, K.; Hajra, A. Chem. Commun. 2015, 51, 1555. [15] Zhao, X.-Y.; Ding, Y.-Y.; Lu, Y.-T.; Kang, C.-M. Chin. J. Org. Chem. 2019, 39, 1304(in Chinese). (赵鑫雨, 丁扬扬, 吕英涛, 康从民, 有机化学, 2019, 39, 1304.) [16] Khajuria, R.; Rasheed, S.; Khajuria, C.; Kapoor, K. K.; Das, P. Synthesis 2018, 50, 2131. [17] Ahneman, D. T.; Estrada, J. G.; Lin, S. S.; Dreher, S. D.; Doyle, A. G. Science 2018, 360, 186. [18] (a) Yang, K.; Qiu, Y.-T.; Li, Z.; Wang, Z.-Y.; Jiang, S. J. Org. Chem. 2011, 76, 3151. (b) Yang, K.; Li, Z.; Wang, Z.-Y.; Yao, Z.-Y.; Jiang, S. Org. Lett. 2011, 13, 4340. [19] Abrams, R.; Lefebvre, Q.; Clayden, J. Angew. Chem., Int. Ed. 2018, 57, 13587. [20] Venkatesh, C.; Sundaram, G. S. M.; Ila, H.; Junjappa, H. J. Org. Chem. 2006, 71, 1280. [21] Liubchak, K.; Nazarenko, K.; Tolmachev, A. Tetrahedron 2012, 68, 2993. [22] Chen, F.; Chen, H.; Wu, Q.-A.; Luo, S.-P. Chin. J. Org. Chem. 2020, 40, 339(in Chinese). (陈锋, 陈浩, 吴庆安, 罗书平, 有机化学, 2020, 40, 339.) [23] Barolo, S. M.; Wang, Y.; Rossi, R. A.; Cuny, G. D. Tetrahedron 2013, 69, 5487. [24] Wang, H.-G.; Wang, Y.; Peng, C.-L.; Zhang, J.-C.; Zhu, Q. J. Am. Chem. Soc. 2010, 132, 13217. [25] Masters, K. S.; Rauws, T. R. M.; Yadav, A. K.; Herrebout, W. A.; Van der Veken, B.; Maes, B. U. W. Chem.-Eur. J. 2011, 17, 6315. [26] Wu, Y.-X.; Xi, Y.-C.; Zhao, M.; Wang, S.-Y. Chin. J. Org. Chem. 2018, 38, 2590(in Chinese). (吴亚星, 席亚超, 赵明, 王思懿, 有机化学, 2018, 38, 2590.) [27] (a) Yang, Q. L.; Li, Y. Q.; Ma, C.; Fang, P.; Zhang, X. J.; Mei, T. S. J. Am. Chem. Soc. 2017, 139, 3293. (b) Ma, C.; Fang, P.; Mei, T.-S. ACS Catal. 2018, 8, 7179. (c) Xu, F.; Long, H.; Song, J.; Xu, H. C. Angew. Chem., Int. Ed. 2019, 58, 9017. [28] Duan, Z.-L.; Zhang, L.; Zhang, W.-X.; Lu, L.-J.; Zeng, L.; Shi, R.-Y.; Lei, A.-W. ACS Catal. 2020, 10, 3828. [29] Lv, S.-D.; Han, X.-X.; Wang, J.-Y.; Zhou, M.-Y.; Wu, Y.-W.; Ma, L.; Niu, L.-W.; Gao, W.; Zhou, J.-H.; Hu, W.; Cui, Y.-Z.; Chen, J.-B. Angew. Chem., Int. Ed. 2020, 59, 11573. [30] Xue, F.-L.; Peng, P.; Shi, J.; Zhong, M.-L.; Wang, Z.-Y. Synth. Commun. 2014, 44, 1944. [31] Rao, D. N.; Rasheed, S.; Vishwakarma, R. A.; Das, P. RSC Adv. 2014, 4, 25600. [32] Kutsumura, N.; Kunimatsu, S.; Kagawa, K.; Otani, T.; Saito, T. Synthesis 2011, 3235. [33] Qian, G.-Y.; Liu, B.-X.; Tan, Q.-T.; Zhang, S.-W.; Xu, B. Eur. J. Org. Chem. 2014, 4837. [34] He, Y.-M.; Huang, J.-B.; Liang, D.-D.; Liu, L.-Y.; Zhu, Q. Chem. Commun. 2013, 49, 7352. [35] Liang, D.-D.; He, Y.-M.; Liu, L.-Y.; Zhu, Q. Org. Lett. 2013, 15, 3476. [36] Lv, Z.-G.; Liu, J.; Wei, W.; Wu, J.; Yu, W.-Q.; Chang, J.-B. Adv. Synth. Catal. 2016, 358, 2759. [37] Lee, H. E.; Lee, M. J.; Park, J. K. Asian J. Org. Chem. 2019, 8, 1659. [38] Xu, C.-R.; Wang, K.-X.; Li, D.-W.; Lin, L.-L.; Feng, X.-M. Angew. Chem., Int. Ed. 2019, 58, 18438. [39] (a) Maiti, D.; Fors, B. P; Henderson, J. L.; Nakamura, Y.; Buchwald, S. L. Chem. Sci. 2011, 2, 57. (b) Han, Y.; Zhang, M.; Zhang, Y.-Q.; Zhang, Z.-H. Green Chem. 2018, 20, 4891. [40] Wexler, R. P.; Nuhant, P.; Senter, T. J.; Gale-Day, Z. J. Org. Lett. 2019, 21, 4540. [41] Rasheed, S.; Rao, D. N.; Das, P. J. Org. Chem. 2015, 80, 9321. [42] Yan, H.; Guo, H.; Zhou, X.-Q.; Zuo, Z.-Y.; Liu, J.-L.; Zhang, G.-H.; Zhang, S. Synlett 2019, 30, 1469. [43] (a) Louillat, M. L.; Patureau, F. W. Chem. Soc. Rev. 2014, 43, 901. (b) Li, L.-X.; Li, Y.; Zhao, Z.-G.; Luo, H.-T.; Ma, Y.-N. Org. Lett. 2019, 21, 5995. (c) Matsumoto, M.; Wada, K.; Urakawa, K.; Ishikawa, H. Org. Lett. 2020, 22, 781. [44] Manna, S.; Matcha, K.; Antonchick, A. P. Angew. Chem., Int. Ed. 2014, 53, 8163. [45] Liu, X.-L.; Chen, J.; Ma, T.-L. Org. Biomol. Chem. 2018, 16, 8662. [46] Xie, Y.-J.; Wu, J.; Che, X.-Z.; Chen, Y.; Huang, H.-W.; Deng, G.-J. Green Chem. 2016, 18, 667. [47] Zhang, W.-W.; Li, H.-J.; Wang, M.-R.; Wang, L.-J.; Zhang, A.-H.; Wu, Y.-C. New J. Chem. 2019, 43, 413. [48] Wu, Z.-Q.; Huang, Q.; Zhou, X.-G.; Yu, L.-T.; Li, Z.-K.; Wu, D. Eur. J. Org. Chem. 2011, 5242. [49] Yang, K.; Wang, Z.-Y.; Fu, J.-H.; Tan, Y.-H. Prog. Chem. 2010, 22, 2126(in Chinese). (杨凯, 汪朝阳, 傅建花, 谭越河, 化学进展, 2010, 22, 2126.) [50] Cai, Q.; Li, Z. Q.; Wei, J. J.; Fu, L. B.; Ha, C. Y.; Pei, D. Q.; Ding, K. Org. Lett. 2010, 12, 1500. [51] Zhou, B.-W.; Gao, J.-R.; Jiang, D.; Jia, J.-H.; Yang, Z.-P.; Jin, H.-W. Synthesis 2010, 2794. [52] (a) Huo, J.-P.; Lu, M.-X.; Wang, Z.-Y.; Li, Y.-Z. Chin. J. Chem. 2012, 30, 2411. (b) Tan, Y.-H.; Li, J.-X.; Xue, F.-L.; Qi, J.; Wang, Z.-Y. Tetrahedron 2012, 68, 2827. (c) Tan, Y.-H.; Li, J.-X.; Huo, J.-P.; Xue, F.-L.; Wang, Z.-Y. Synth. Commun. 2014, 44, 2974. (d) Huo, J.-P.; Wei, X.-P.; Mo, G.-Z.; Peng, P.; Zhong, M.-L.; Chen, R.-H.; Wang, Z.-Y. Chin. J. Org. Chem. 2014, 34, 92(in Chinese). (霍景沛, 韦新平, 莫广珍, 彭湃, 钟铭丽, 陈任宏, 汪朝阳, 有机化学, 2014, 34, 92.) [53] Moses, J. E.; Moorhouse, A. D. Chem. Soc. Rev. 2016, 45, 6888. [54] Nagesh, H. N.; Suresh, A.; Reddy, M. N.; Suresh, N.; Subbalakshmi, J.; Sekhar, K. V. G. C. RSC Adv. 2016, 6, 15884. [55] Kato, J.; Ito, Y.; Ijuin, R.; Aoyama, H.; Yokomatsu, T. Org. Lett. 2013, 15, 3794. [56] da Silva, R. B.; Coelho, F. L.; Rodembusch, F. S.; Schwab, R. S.; Schneider, J. M. F. M.; Rampon, D. D.; Schneider, P. H. New J. Chem. 2019, 43, 11596. [57] Yin, C.-X.; Huo, F.-J.; Cooley, N. P.; Spencer, D.; Bartholomew, K.; Barnes, C. L.; Glass, T. E. ACS Chem. Neurosci. 2017, 8, 1159. [58] Panda, K.; Suresh, J. R.; Ila, H.; Junjappa, H. J. Org. Chem. 2003, 68, 3498. [59] Kotovskaya,S. K.; Baskakova, Z. M.; Charushin, V. N.; Chupakhin, O. N.; Belanov, E. F.; Bormotov, N. I.; Balakhnin, S. M.; Serova. O. A. Pharm. Chem. J. 2005, 39, 574. [60] Shaaban, M. R.; Eldebss, T. M. A.; Darweesh, A. F.; Farag, A. M. J. Heterocycl. Chem. 2008, 45, 1739. [61] Ibrahim, M. A. Tetrahedron 2013, 69, 6861. [62] Goli-Garmroodi, F.; Omidi, M.; Saeedi, M.; Sarrafzadeh, F.; Rafinejad, A.; Mahdavi, M.; Bardajee, G. R.; Akbarzadeh, T.; Firoozpour, L.; Shafiee, A.; Foroumadi, A. Tetrahedron Lett. 2015, 56, 743. [63] Tireli, M.; Starcevic, K.; Martinovic, T.; Pavelic, S. K.; Karminski-Zamola, G.; Hranjec, M. Mol. Diversity 2017, 21, 201. [64] Vodolazhenko, M. A.; Mykhailenko, A. E.; Gorobets, N. Y.; Desenko, S. M. J. Heterocycl. Chem. 2017, 54, 753. [65] Lyons, D. M.; Huttunen, K. M.; Browne, K. A.; Ciccone, A.; Trapani, J. A.; Denny, W. A.; Spicer, J. A. Bioorg. Med. Chem. 2011, 19, 4091. [66] Jardosh, H. H.; Sangani, C. B.; Patel, M. P.; Patel, R. G. Chin. Chem. Lett. 2013, 24, 123. [67] Teng, Q.-H.; Peng, X.-J.; Mo, Z.-Y.; Xu, Y.-L.; Tang, H.-T.; Wang, H.-S.; Sun, H.-B.; Pan, Y.-M. Green Chem. 2018, 20, 2007. [68] Jiang, Z.-Q.; Miao, D. Z.; Tong, Y.; Pan, Q.; Li, X.-T.; Hu, R.-H.; Han, S.-Q. Synthesis 2015, 47, 1913. [69] Ge, Y.-Q.; Jia, J.; Yang, H.; Tao, X.-T.; Wang, J.-W. Dyes Pigm. 2011, 88, 344. [70] Yang, H.; Ge, Y.-Q.; Jia, J.; Wang, J.-W. J. Lumin. 2011, 131, 749. [71] Peng, J.-S.; Shang, G.-N.; Chen, C.-X.; Miao, Z.-S.; Li, B. J. Org. Chem. 2013, 78, 1242. [72] Zheng, L.-Y.; Hua, R.-M. J. Org. Chem. 2014, 79, 3930. [73] Ghosh, K.; Nishii, Y.; Miura, M. ACS Catal. 2019, 9, 11455. [74] Mai, S.-Y.; Luo, Y.-X.; Huang, X.-Y.; Shu, Z.-H.; Li, B.-N.; Lan, Y.; Song, Q.-L. Chem. Commun. 2018, 54, 10240. [75] Miao, W.-Q.; Liu, J.-Q.; Wang, X.-S. Org. Biomol. Chem. 2017, 15, 5325. [76] Liu, J.-M.; Zhang, N.-F.; Yue, Y.-Y.; Liu, G.-H.; Liu, R.; Zhang, Y.-L.; Zhuo, K.-L. Eur. J. Org. Chem. 2013, 7683. [77] Yan, L.-P.; Zhao, D.-B.; Lan, J.-B.; Cheng, Y.-Y.; Guo, Q.; Li, X.-Y.; Wu, N.-J.; You, J.-S. Org. Biomol. Chem. 2013, 11, 7966. [78] Chen, C.-X.; Shang, G.-N.; Zhou, J.-J.; Yu, Y.-H.; Li, B.; Peng, J.-S. Org. Lett. 2014, 16, 1872. [79] Zhao, G.-Y.; Chen, C.-X.; Yue, Y.-X.; Yu, Y.-H.; Peng, J.-S. J. Org. Chem. 2015, 80, 2827. [80] Li, X.; Chen, X.; Wang, H.; Chen, C.-X.; Sun, P.; Mo, B.-C.; Peng, J.-S. Org. Biomol. Chem. 2019, 17, 4014. [81] Bera, S. K.; Alam, M. T.; Mal, P. J. Org. Chem. 2019, 84, 12009. [82] Wezeman, T.; Scopelliti, R.; Tirani, F. F.; Severin, K. Adv. Synth. Catal. 2019, 361, 1383. [83] Huang, J.-R.; Dong, L.; Han, B.; Peng, C.; Chen, Y.-C. Chem.-Eur. J. 2012, 18, 8896. [84] Dong, L.; Huang, J.-R.; Qu, C.-H.; Zhang, Q.-R.; Zhang, W.; Han, B.; Peng, C. Org. Biomol. Chem. 2013, 11, 6142. [85] Ghorai, D.; Choudhury, J. Chem. Commun. 2014, 50, 15159. [86] Thenarukandiyil, R.; Dutta, C.; Choudhury, J. Chem.-Eur. J. 2017, 23, 15529. [87] Morioka, R.; Nobushige, K.; Satoh, T.; Hirano, K.; Miura, M. Org. Lett. 2015, 17, 3130. [88] Reddy, V. P.; Iwasaki, T.; Kambe, N. Org. Biomol. Chem. 2013, 11, 2249. [89] Sun, M.-M.; Wu, H.-D.; Zheng, J.-N.; Bao, W.-L. Adv. Synth. Catal. 2012, 354, 835. [90] Chen, L.; Zhang, X.; Chen, B.; Li, B.; Li, Y.-B. Chem. Heterocycl. Compd. 2017, 53, 618. [91] Reddy, C. R.; Burra, A. G. J. Org. Chem. 2019, 84, 9169. [92] Peng, H.-B.; Yu, J.-T.; Jiang, Y.; Wang, L.; Cheng, J. Org. Biomol. Chem. 2015, 13, 5354. [93] Li, P.-Y.; Zhang, X.-Y.; Fan, X.-S. J. Org. Chem. 2015, 80, 7508. [94] Qi, Z.-S.; Yu, S.-J.; Li, X.-W. J. Org. Chem. 2015, 80, 3471. [95] Xue, C.-W.; Han, J.-W.; Zhao, M.; Wang, L.-M. Org. Lett. 2019, 21, 4402. [96] (a) Mao, Z.-Z.; Wang, Z.-Y.; Hou, X.-N.; Song, X.-M.; Luo, Y.-F. Chin. J. Org. Chem. 2008, 28, 542(in Chinese). (毛郑州, 汪朝阳, 侯晓娜, 宋秀美, 罗玉芬, 有机化学, 2008, 28, 542.) (b) Peng, P.; Xiong, J.-F.; Li, B.; Mo, G.-Z.; Chen, R.-H.; Wang, Z.-Y. Chin. J. Org. Chem. 2013, 33, 1891(in Chinese). (彭湃, 熊金锋, 李豹, 莫广珍, 陈任宏, 汪朝阳, 有机化学, 2013, 33, 1891.) (c) Wu, Y.-C.; You, J.-Y.; Guan, L.-T.; Shi, J.; Cao, L.; Wang, Z.-Y. Chin. J. Org. Chem. 2015, 35, 2465(in Chinese). (吴彦城, 尤嘉宜, 关丽涛, 石杰, 曹梁, 汪朝阳, 有机化学, 2015, 35, 2465.) (d) Wang, N.; Arulkumar, M.; Chen, X.-Y.; Wang, B.-W.; Chen, S.-H.; Yao, C.; Wang, Z.-Y. Chin. J. Org. Chem. 2019, 39, 2771(in Chinese). (王能, Arulkumar, M., 陈孝云, 王柏文, 陈思鸿, 姚辰, 汪朝阳,有机化学, 2019, 39, 2771.) [97] (a) Wu, Y.-C.; Huo, J.-P.; Cao, L.; Ding, S.; Wang, L.-Y.; Cao, D.-R.; Wang, Z.-Y. Sens. Actuators, B 2016, 237, 865. (b) Wu, Y.-C.; Luo, S.-H.; Cao, L.; Jiang, K.; Wang, L.-Y.; Xie, J.-C.; Wang, Z.-Y. Anal. Chim. Acta 2017, 976, 74. (c) Pang, C.-M.; Luo, S.-H.; Jiang, K.; Wang, B.-W.; Chen, S.-H.; Wang, N.; Wang, Z.-Y. Dyes Pigm. 2019, 170, 107651. [98] Milisiunaite, V.; Arbaciauskiene, E.; Bieliauskas, A.; Vilkauskaite, G.; Sackus, A.; Holzer, W. Tetrahedron 2015, 71, 3385. [99] Rustagi, V.; Aggarwal, T.; Verma, A. K. Green Chem. 2011, 13, 1640. [100] Rustagi, V.; Tiwari, R.; Verma, A. K. Eur. J. Org. Chem. 2012, 4590. [101] Ouyang, H.-C.; Tang, R.-Y.; Zhong, P.; Zhang, X.-G.; Li, J.-H. J. Org. Chem. 2011, 76, 223. [102] Gvozdev, V. D.; Shavrin, K. N.; Baskir, E. G.; Egorov, M. P.; Nefedov, O. M. Mendeleev Commun. 2017, 27, 231. [103] Chaitanya, T. K.; Prakash, K. S.; Nagarajan, R. Tetrahedron 2011, 67, 6934. [104] Mishra, M.; Twardy, D.; Ellstrom, C.; Wheeler, K. A.; Dembinski, R.; Török, B. Green Chem. 2019, 21, 99. [105] Adib, M.; Zainali, M.; Kim, I. Synlett 2016, 27, 1844. [106] Yan, C.-G.; Wang, Q.-F.; Song, X.-K.; Sun, J. J. Org. Chem. 2009, 74, 710. [107] Hu, Y.; Wang, T.; Liu, Y.-Z.; Nie, R.-F.; Yang, N.-H.; Wang, Q.-T.; Li, G.-B.; Wu, Y. Org. Lett. 2020, 22, 501. |
[1] | Hongqiong Zhao, Miao Yu, Dongxue Song, Qi Jia, Yingjie Liu, Yubin Ji, Ying Xu. Progress on Decarboxylation and Hydroxylation of Carboxylic Acids [J]. Chinese Journal of Organic Chemistry, 2024, 44(1): 70-84. |
[2] | Guangli Xu, Jing Xu, Haidong Xu, Xiang Cui, Xingzhong Shu. Research Progress of Transition Metal Catalyzed Synthesis of 1,3- Conjugated Diene Compounds from Alkenes and Alkynes [J]. Chinese Journal of Organic Chemistry, 2023, 43(6): 1899-1933. |
[3] | Xiaojing Hu, Feixiang Guo, Runqing Zhu, Bingqi Zhou, Tao Zhang, Lizhen Fang. Synthesis of p-Alkoxy Phenol and Its Application after Dearomatization [J]. Chinese Journal of Organic Chemistry, 2023, 43(6): 2239-2244. |
[4] | Kongchuan Wu, Kaihong Lu, Jianbin Lin, Huijun Zhang. Research Progress in Ortho-C—H Bond Functionalization of Rylene Diimides [J]. Chinese Journal of Organic Chemistry, 2023, 43(3): 1000-1011. |
[5] | Hairui Jia, Zaozao Qiu. Recent Advances in Transition Metal-Catalyzed B—H Bond Activation for Synthesis of o-Carborane Derivatives with B—Heteroatom Bond [J]. Chinese Journal of Organic Chemistry, 2023, 43(3): 1045-1068. |
[6] | Ling Meng, Jun Wang. Research Progress on Synthesis of Thioflavonoids [J]. Chinese Journal of Organic Chemistry, 2023, 43(3): 873-891. |
[7] | Yan Zeng, Fei Ye. Research Progress on New Catalytic Reaction Systems for Asymmetric Synthesis of Silicon-Stereogenic Center Containing Compounds [J]. Chinese Journal of Organic Chemistry, 2023, 43(10): 3388-3413. |
[8] | Min Liu, Liping Qi, Dongbing Zhao. Recent Advances in Transition Metal-Catalyzed C—Si Bond Cleavage of Silacyclobutanes [J]. Chinese Journal of Organic Chemistry, 2023, 43(10): 3508-3525. |
[9] | Donghan Liu, Xihang Lu, Zhangmengjie Chai, Haoqi Yang, Yulin Sun, Fuchao Yu. Progress in Construction of 2H-Pyrrol-2-ones Skeleton [J]. Chinese Journal of Organic Chemistry, 2023, 43(1): 57-73. |
[10] | Jinyu Zhang, Tianfen Liu, Le Wang, Xiaoming Wang. Recent Process in the in situ Generated Metal Nanocluster Catalysis [J]. Chinese Journal of Organic Chemistry, 2022, 42(8): 2331-2341. |
[11] | Jinsong Hou, Gaosheng Yang. Reaction of Tandem Addition of Aliphatic Amines to Alkenylnitriles Catalyzed by Tris(o-dimethylaminobenzyl)yttrium [J]. Chinese Journal of Organic Chemistry, 2022, 42(7): 2070-2078. |
[12] | Yuanhao Mao, Yanfeng Gao, Zhiwei Miao. Research Progress on the Asymmetric Cyclization Synthesis of Seven-Membered Rings via Transition Metal Catalysis [J]. Chinese Journal of Organic Chemistry, 2022, 42(7): 1904-1924. |
[13] | Fei Yuan, Yan Zhao, Qingsong Guo, Fudan Yin, Jinrong Lai, Beifang Nian, Ming Zhang, E Tang. Synthesis of 1-[1-(Amino)cyclopropyl]ketones by Tandem Reaction Involving Vinyl Selenium Salt [J]. Chinese Journal of Organic Chemistry, 2022, 42(6): 1759-1769. |
[14] | Ning Chen, Jia Lei, Zhichuan Wang, Yingjie Liu, Kai Sun, Shi Tang. Construction of Fluoro-containing Heterocycles Mediated by Free Radicals [J]. Chinese Journal of Organic Chemistry, 2022, 42(4): 1061-1084. |
[15] | Huijie Qiao, Liting Yang, Ya Chen, Jialin Wang, Wuxuan Sun, Haobo Dong, Yunwei Wang. An Efficient Three-Component Tandem Approach for the Synthesis of Imidazoheterocycle-Hydrazine Derivatives under Mild Conditions [J]. Chinese Journal of Organic Chemistry, 2022, 42(4): 1188-1197. |
Viewed | ||||||
Full text |
|
|||||
Abstract |
|
|||||