Chinese Journal of Organic Chemistry ›› 2022, Vol. 42 ›› Issue (4): 925-944.DOI: 10.6023/cjoc202109020 Previous Articles Next Articles
REVIEWS
收稿日期:
2021-09-14
修回日期:
2021-11-16
发布日期:
2021-12-02
通讯作者:
赵常贵
基金资助:
Ting Yao, Jiayan Li, Jiaming Wang, Changgui Zhao()
Received:
2021-09-14
Revised:
2021-11-16
Published:
2021-12-02
Contact:
Changgui Zhao
Supported by:
Share
Ting Yao, Jiayan Li, Jiaming Wang, Changgui Zhao. Recent Advances for the Construction of Seven-Membered Ring Catalyzed by N-Heterocyclic Carbenes[J]. Chinese Journal of Organic Chemistry, 2022, 42(4): 925-944.
[1] |
(a) Ratnayake, R.; Covell, D.; Ransom, T. T.; Gustafson, K. R.; Beutler, J. A. Org. Lett. 2009, 11, 57.
doi: 10.1021/ol802339w pmid: 19061394 |
(b) Cragg, G. M.; Newman, D. J. Phytochem. Rev. 2009, 8, 313.
doi: 10.1007/s11101-009-9123-y pmid: 19061394 |
|
(c) Drew, D. P.; Krichau, N.; Reichwald, K.; Simonsen, H. T. Phytochem. Rev. 2009, 8, 581.
doi: 10.1007/s11101-009-9130-z pmid: 19061394 |
|
(d) Li, Z.; Nakashige, M.; Chain, W. J. J. Am. Chem. Soc. 2011, 133, 6553.
doi: 10.1021/ja201921j pmid: 19061394 |
|
(e) Wu, D.; He, Q.; Chen, D.; Ye, J.; Huang, P. Chin. J. Chem. 2019, 37, 315.
doi: 10.1002/cjoc.201900035 pmid: 19061394 |
|
[2] |
(a) Wang, Y.; Ju, W.; Tian, H.; Tian, W.; Gui, J. J. Am. Chem. Soc. 2018, 140, 9413.
doi: 10.1021/jacs.8b06444 pmid: 24869712 |
(b) Amagata, T.; Amagata, A.; Tenney, K.; Valeriote, F. A.; Lobkovsky, E.; Clardy, J.; Crews, P. Org. Lett. 2003, 5, 4393.
pmid: 24869712 |
|
(c) Biellmann, J. F. Chem. Rev. 2003, 103, 2019.
doi: 10.1021/cr020071b pmid: 24869712 |
|
(d) Sarma, N. S.; Krishna, M. S.; Pasha, S. G.; Rao, T. S. P.; Venkateswarlu, Y.; Parameswaran, P. S. Chem. Rev. 2009, 109, 2803.
doi: 10.1021/cr800503e pmid: 24869712 |
|
(e) Bansal, R.; Acharya, P. C. Chem. Rev. 2014, 114, 6986.
doi: 10.1021/cr4002935 pmid: 24869712 |
|
(f) Wu, J.; Liu, J.; Fan, J.; Xie, Z.; Qin, H.; Li, C. Chin. J. Chem. 2021, 39, 1247.
doi: 10.1002/cjoc.202000698 pmid: 24869712 |
|
[3] |
(a) Dokkedal-Silva, V.; Berro, L. F.; Galduróz, J. C. F.; Tufik, S.; Andersen, M. L. Harv. Rev. Psychiatry 2019, 27, 279.
doi: 10.1097/HRP.0000000000000227 pmid: 26109227 |
(b) Huang, Y.; Fu, Z. Heart 2011, 97, 217.
pmid: 26109227 |
|
(c) Cheng, L. H.; Lee, J. C.; Wu, P. C.; Lin, Y. Y.; Chu, Y. H.; Wang, H. W. Rhinology 2019, 57, 268.
doi: 10.4193/Rhin18.274 pmid: 26109227 |
|
(d) Perna, G.; Alciati, A.; Riva, A.; Micieli, W.; Caldirola, D. Curr. Psychiatry Rep. 2016, 18, 23.
doi: 10.1007/s11920-016-0668-3 pmid: 26109227 |
|
(e) Shangguan, Y.; Liao, H.; Wang, X. Expert Rev. Neurother. 2015, 15, 733.
doi: 10.1586/14737175.2015.1056781 pmid: 26109227 |
|
(f) Li, J.; Hao, Z.; Zhang, K.; Wang, L. Chin. J. Org. Chem. 2021, 41, 806. (in Chinese)
doi: 10.6023/cjoc202006040 pmid: 26109227 |
|
( 李静, 郝振芳, 张凯悦, 王兰芝, 有机化学, 2021, 41, 806.)
doi: 10.6023/cjoc202006040 pmid: 26109227 |
|
(g) Yang, W.; Huang, Z.; Liu, Y.; Yu, X.; Deng, W. Chin. J. Chem. 2020, 38, 1571.
doi: 10.1002/cjoc.202000264 pmid: 26109227 |
|
(h) 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)
doi: 10.6023/cjoc201904061 pmid: 26109227 |
|
( 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.)
doi: 10.6023/cjoc201904061 pmid: 26109227 |
|
(i) Zhang, X.; Wang, Y.; Chen, P.; Cai, X.; Jia, Y. Chin. J. Chem. 2021, 39, 1983.
doi: 10.1002/cjoc.202100001 pmid: 26109227 |
|
(j) Hou, B.; Li, J.; Xin, H.; Yang, X.; Gao, H.; Peng, P.; Gao, X. Acta Chim. Sinica 2020, 78, 788. (in Chinese)
doi: 10.6023/A20050161 pmid: 26109227 |
|
( 侯斌, 李晶, 辛涵申, 杨笑迪, 高洪磊, 彭培珍, 高希珂, 化学学报, 2020, 78, 788.)
doi: 10.6023/A20050161 pmid: 26109227 |
|
[4] |
(a) Yet, L. Chem. Rev. 2000, 100, 2963.
pmid: 11749312 |
(b) Zhu, C.; Yang, B.; Mai, B. K.; Palazzotto, S.; Qiu, Y.; Gudmundsson, A.; Ricke, A.; Himo, F.; Bäckvall, J. J. Am. Chem. Soc. 2018, 140, 14324.
doi: 10.1021/jacs.8b08708 pmid: 11749312 |
|
(c) Pulido, F. J.; Barbero, A.; Castreño, P. J. Org. Chem. 2011, 76, 5850.
doi: 10.1021/jo200705u pmid: 11749312 |
|
(d) Ali, B. E.; Okuro, K.; Vasapollo, G.; Alper, H. J. Am. Chem. Soc. 1996, 118, 4264.
doi: 10.1021/ja953403l pmid: 11749312 |
|
(e) Ishibashi, T.; Ochifuji, N.; Mori, M. Tetrahedron Lett. 1996, 37, 6165.
doi: 10.1016/0040-4039(96)01338-X pmid: 11749312 |
|
(f) Kumari, P.; Liu, W.; Wang, C. J.; Dai, J.; Wang, M. X.; Yang, Q. Q.; Deng, Y. H.; Shao, Z. Chin. J. Chem. 2020, 38, 151.
doi: 10.1002/cjoc.201900430 pmid: 11749312 |
|
[5] |
(a) Battiste, M. A.; Pelphrey, P. M.; Wright, D. L. Chem.-Eur. J. 2006, 12, 3438.
pmid: 33576620 |
(b) Saito, S.; Komagawa, S.; Azumaya, I.; Masuda, M. J. Org. Chem. 2007, 72, 9114.
doi: 10.1021/jo7014714 pmid: 33576620 |
|
(c) Wender, P. A.; Glorius, F.; Husfeld, C. O.; Langkopf, E.; Love, J. A. J. Am. Chem. Soc. 1999, 121, 5348.
doi: 10.1021/ja9903072 pmid: 33576620 |
|
(d) Doerksen, R. S.; Hodík, T.; Hu, G.; Huynh, N. O.; Shuler, W. G.; Krische, M. J. Chem. Rev. 2021, 121, 4045.
doi: 10.1021/acs.chemrev.0c01133 pmid: 33576620 |
|
(e) Trost, B. M.; Zuo, Z.; Schultz, J. E. Chemistry 2020, 26, 15354.
pmid: 33576620 |
|
(f) Kuila, B.; Kaur, M.; Singh, P.; Bhargava, G. Eur. J. Org. Chem. 2018, 7, 853.
pmid: 33576620 |
|
[6] |
(a) Li, X.; Zhang, Z.; Fan, H.; Miao, Y.; Tian, H.; Gu, Y.; Gui, J. J. Am. Chem. Soc. 2021, 143, 4886.
doi: 10.1021/jacs.0c13426 |
(b) Davies, H. M. L.; Oldenburg, C. E. M.; McAfee, M. J.; Nordahl, J. G.; Henretta, J. P.; Romines, K. R. Tetrahedron Lett. 1988, 29, 975.
doi: 10.1016/0040-4039(88)85312-7 |
|
(c) Nakata, T.; Nomura, S.; Matsukura, H. Tetrahedron Lett. 1996, 37, 213.
|
|
(d) Wang, R. Q.; Shen, C.; Cheng, X.; Wang, Z. F.; Tao, H. Y.; Dong, X. Q.; Wang, C. J. Chin. J. Chem. 2020, 38, 807.
doi: 10.1002/cjoc.202000065 |
|
[7] |
(a) Flanigan, D. M.; Romanov-Michailidis, F.; White, N. A.; Rovis, T. Chem. Rev. 2015, 115, 9307.
doi: 10.1021/acs.chemrev.5b00060 pmid: 25992594 |
(b) Menon, R. S.; Biju, A. T.; Nair, V. Chem. Soc. Rev. 2015, 44, 5040.
doi: 10.1039/C5CS00162E pmid: 25992594 |
|
(c) He, L.; Jian, T. Y.; Ye, S. J. Org. Chem. 2007, 72, 7466.
doi: 10.1021/jo071247i pmid: 25992594 |
|
(d) Rong, Z. Q.; Jia, M. Q.; You, S. L. Org. Lett. 2011, 13, 4080.
doi: 10.1021/ol201595f pmid: 25992594 |
|
(e) Ohmiya, H. ACS Catal. 2020, 10, 6862.
doi: 10.1021/acscatal.0c01795 pmid: 25992594 |
|
(f) Nagao, K.; Ohmiya, H. Top Curr. Chem. 2019, 377, 35.
pmid: 25992594 |
|
(g) Patra, A.; Mukherjee, S.; Das, T. K.; Jain, S.; Gonnade, R. G.; Biju, A. T. Angew. Chem., Int. Ed. 2017, 56, 2730.
doi: 10.1002/anie.201611268 pmid: 25992594 |
|
(h) Zhang, Z. J.; Wen, Y. H.; Song, J.; Gong, L. Z. Angew. Chem., Int. Ed. 2021, 60, 3268.
doi: 10.1002/anie.202013679 pmid: 25992594 |
|
(i) Liu, Q.; Chen, X. Y.; Puttreddy, R.; Rissanen, K.; Enders, D. Angew. Chem., Int. Ed. 2018, 57, 17100.
doi: 10.1002/anie.201810402 pmid: 25992594 |
|
(j) Ryan, S. J.; Candish, L.; Lupton, D. W. Chem. Soc. Rev. 2013, 42, 4906.
doi: 10.1039/c3cs35522e pmid: 25992594 |
|
(k) Wang, A.; Xiao, Y.; Zhou, Y.; Xu, J.; Liu, H. Chin. J. Org. Chem. 2017, 37, 2590. (in Chinese)
pmid: 25992594 |
|
( 王翱, 肖永龙, 周宇, 徐进宜, 柳红, 有机化学, 2017, 37, 2590.)
doi: 10.6023/cjoc201702041 pmid: 25992594 |
|
(l) Qu, M.; He, J. Chin. J. Org. Chem. 2011, 31, 1388. (in Chinese)
pmid: 25992594 |
|
( 屈孟男, 何金梅, 有机化学, 2011, 31, 1388.)
pmid: 25992594 |
|
(m) Zhao, C.; Blaszczyk, S. A.; Wang, J. Green Synth. Catal. 2021, 2, 198.
pmid: 25992594 |
|
(n) Chen, X.; Wang, H.; Jin, Z.; Chi, Y. R. Chin. J. Chem. 2020, 38, 1167.
doi: 10.1002/cjoc.202000107 pmid: 25992594 |
|
(o) Liu, Q.; Zhang, X.; Zhao, Z.; Li, X.; Zhang, W. Chin. J. Chem. 2021, 39, 605
doi: 10.1002/cjoc.202000237 pmid: 25992594 |
|
[8] |
(a) He, J.; Tang, S.; Liu, J.; Su, Y.; Pan, X.; She, X. Tetrahedron 2008, 64, 8797.
doi: 10.1016/j.tet.2008.06.082 |
(b) He, J.; Tang, S.; Tang, S.; Liu, J.; Sun, Y.; Pan, X.; She, X. Tetrahedron Lett. 2009, 28, 430.
|
|
[9] |
(a) Zhang, Y. R.; He, L.; Wu, X.; Shao, P. L.; Ye, S. Org. Lett. 2008, 10, 277.
doi: 10.1021/ol702759b |
(b) Zhang, Y. R.; Lv, H.; Zhou, D.; Ye, S. Chem.-Eur. J. 2008, 14, 8473.
doi: 10.1002/chem.200801165 |
|
(c) Shao, P. L.; Chen, X. Y.; Ye, S. Angew. Chem., Int. Ed. 2010, 49, 8412.
doi: 10.1002/anie.201003532 |
|
[10] |
(a) Sarkar, S. D.; Studer, A. Angew. Chem., Int. Ed. 2010, 49, 9266.
doi: 10.1002/anie.201004593 |
(b) Xie, D.; Shen, D.; Chen, Q.; Zhou, J.; Zeng, X.; Zhong, G. J. Org. Chem. 2016, 81, 6136.
doi: 10.1021/acs.joc.6b01152 |
|
(c) Wu, S.; Liu, C.; Luo, G.; Jin, Z.; Zheng, P.; Chi, Y. R. Angew. Chem., Int. Ed. 2019, 58, 18410.
doi: 10.1002/anie.201909479 |
|
(d) Wang, J.; Li, Y.; Sun, J.; Wang, H.; Jin, Z.; Chi, Y. R. ACS Catal. 2018, 8, 9859.
doi: 10.1021/acscatal.8b02651 |
|
(e) Liu, C.; Wu, S.; Xu, J.; Chen, L.; Zheng, P.; Chi, Y. R. Org. Lett. 2019, 21, 9493.
doi: 10.1021/acs.orglett.9b03685 |
|
[11] |
(a) Guo, F.; Chen, J.; Huang, Y. ACS Catal. 2021, 11, 6316.
doi: 10.1021/acscatal.1c01908 |
(b) Chen, J.; Meng, S.; Wang, L.; Tang, H.; Huang, Y. Chem. Sci. 2015, 6, 4184.
doi: 10.1039/C5SC00878F |
|
(c) Wang, L.; Chen, J.; Huang, Y. Angew. Chem., Int. Ed. 2015, 54, 15414.
doi: 10.1002/anie.201508371 |
|
[12] |
(a) Bie, J.; Lang, M.; Wang, J. Org. Lett. 2018, 20, 5866.
doi: 10.1021/acs.orglett.8b02538 |
(b) Yang, G.; Guo, D.; Meng, D.; Wang, J. Nat. Commun. 2019, 10, 3062.
doi: 10.1038/s41467-019-10878-7 |
|
(c) Xu, K.; Li, W.; Zhu, S.; Zhu, T. Angew. Chem., Int. Ed. 2019, 58, 17625.
doi: 10.1002/anie.201910049 |
|
(d) Zhao, Q.; Jiang, R.; You, S. Acta Chim. Sinica 2021, 79, 1107. (in Chinese)
doi: 10.6023/A21070320 |
|
( 赵庆如, 蒋茹, 游书力, 化学学报, 2021, 79, 1107.)
doi: 10.6023/A21070320 |
|
[13] |
(a) He, H.; Liu, W. B.; Dai, L. X.; You, S. L. Angew. Chem., Int. Ed. 2010, 49, 1496.
doi: 10.1002/anie.200906638 pmid: 27093370 |
(b) Wyatt, P. G.; Allen, M. J.; Chilcott, J.; Hickin, G.; Miller, N. D.; Woollard, P. M. Bioorg. Med. Chem. Lett. 2001, 11, 1301.
pmid: 27093370 |
|
(c) Huang, L.; Dai, L.; You, S. J. Am. Chem. Soc. 2016, 138, 5793.
doi: 10.1021/jacs.6b02678 pmid: 27093370 |
|
[14] |
Siddiqui, I.; Srivastava, A.; Shamim, S.; Srivastava, A.; Shireen.; Waseem, M.; Singh, R. Synlett 2013, 24, 2586.
doi: 10.1055/s-0033-1339894 |
[15] |
Guo, C.; Sahoo, B.; Daniliuc, C. G.; Glorius, F. J. Am. Chem. Soc. 2014, 136, 17402.
doi: 10.1021/ja510737n |
[16] |
Wang, M.; Huang, Z.; Xu, J.; Chi, Y. R. J. Am. Chem. Soc. 2014, 136, 1214.
doi: 10.1021/ja411110f |
[17] |
Wang, L.; Li, S.; Blumel, M.; Philipps, A. R.; Wang, A.; Puttreddy, R.; Rissanen, K.; Enders, D. Angew. Chem., Int. Ed. 2016, 55, 11110.
doi: 10.1002/anie.201604819 |
[18] |
Gao, Z. H.; Chen, K. Q.; Zhang, Y.; Kong, L. M.; Li, Y.; Ye, S. J. Org. Chem. 2018, 83, 15225.
doi: 10.1021/acs.joc.8b02497 |
[19] |
Gao, J. X.; Wang, Y. Org. Biomol. Chem. 2019, 17, 7442.
doi: 10.1039/C9OB01317B |
[20] |
Chen, K. Q.; Gao, Z. H.; Ye, S. Org. Chem. Front. 2019, 6, 405.
doi: 10.1039/C8QO01302K |
[21] |
Fang, C.; Cao, J.; Sun, K.; Zhu, J. D.; Lu, T.; Du, D. Chem.-Eur. J. 2018, 24, 2103.
doi: 10.1002/chem.201705050 |
[22] |
Lang, M.; Wang, J. Eur. J. Org. Chem. 2018, 23, 2958.
|
[23] |
Liu, D.; Hu, Z.; Zhang, Y.; Gong, M.; Fu, Z.; Huang, W. Chem.-Eur. J. 2019, 25, 11223.
|
[24] |
Wu, X.; Zhou, L.; Maiti, R.; Mou, C.; Pan, L.; Chi, Y. R. Angew. Chem., Int. Ed. 2019, 58, 477.
doi: 10.1002/anie.201810879 |
[25] |
Zhu, S. Y.; Zhang, Y.; Chen, X. F.; Huang, J.; Shi, S. H.; Hui, X. P. Chem. Commun. 2019, 55, 4363.
doi: 10.1039/C9CC01444F |
[26] |
(a) Padwa, A.; Boonsombat, J.; Rashatasakhon, P.; Willis, J. Org. Lett. 2005, 7, 3725.
doi: 10.1021/ol0513589 pmid: 24007549 |
(b) Wu, Y. B.; Ni, Z. Y.; Shi, Q. W.; Dong, M.; Kiyota, H.; Gu, Y. C.; Cong, B. Chem. Rev. 2012, 112, 5967.
doi: 10.1021/cr200058f pmid: 24007549 |
|
(c) Moridi Farimani, M.; Nejad Ebrahimi, S.; Salehi, P.; Bahadori, M. B.; Sonboli, A.; Khavasi, H. R.; Zimmermann, S.; Kaiser, M.; Hamburger, M. J. Nat. Prod. 2013, 76, 1806.
doi: 10.1021/np400337a pmid: 24007549 |
|
[27] |
Yang, L.; Tan, B.; Wang, F.; Zhong, G. J. Org. Chem. 2009, 74, 1744.
doi: 10.1021/jo802515g |
[28] |
Rose, C. A.; Zeitler, K. Org. Lett. 2010, 12, 4552.
doi: 10.1021/ol101854r |
[29] |
Lv, H.; Jia, W. Q.; Sun, L. H.; Ye, S. Angew. Chem., Int. Ed. 2013, 52, 8607.
doi: 10.1002/anie.201303903 |
[30] |
Izquierdo, J.; Orue, A.; Scheidt, K. A. J. Am. Chem. Soc. 2013, 135, 10634.
doi: 10.1021/ja405833m pmid: 23829462 |
[31] |
Wang, M.; Rong, Z. Q.; Zhao, Y. Chem. Commun. 2014, 50, 15309.
doi: 10.1039/C4CC07788A |
[32] |
Liang, Z. Q.; Gao, Z. H.; Jia, W. Q.; Ye, S. Chem.-Eur. J. 2015, 21, 1868.
doi: 10.1002/chem.201405828 |
[33] |
Liang, Z. Q.; Yi, L.; Chen, K. Q.; Ye, S. J. Org. Chem. 2016, 81, 4841.
doi: 10.1021/acs.joc.6b00313 |
[34] |
Wang, Z. Y.; Ding, Y. L.; Li, S. N.; Cheng, Y. J. Org. Chem. 2016, 81, 11871.
doi: 10.1021/acs.joc.6b02329 |
[35] |
Li, W.; Yuan, H.; Liu, Z.; Zhang, Z.; Cheng, Y.; Li, P. Adv. Synth. Catal. 2018, 360, 2460.
doi: 10.1002/adsc.201800337 |
[36] |
Xia, F.; Chen, X. Y.; Ye, S. J. Org. Chem. 2018, 83, 15178.
doi: 10.1021/acs.joc.8b02460 |
[37] |
(a) Zhao, M.; Zhang, Y. T.; Chen, J.; Zhou, L. Asian J. Org. Chem. 2018, 7, 54.
doi: 10.1002/ajoc.201700538 |
(b) Lu, H.; Liu, J. Y.; Li, H. Y.; Xu, P. F. Acta Chim. Sinica 2018, 76, 831. (in Chinese)
doi: 10.6023/A18060232 |
|
( 鲁鸿, 刘金宇, 李红玉, 许鹏飞, 化学学报, 2018, 76, 831.)
doi: 10.6023/A18060232 |
|
[38] |
Guo, C.; Fleige, M.; Janssen-Muller, D.; Daniliuc, C. G.; Glorius, F. J. Am. Chem. Soc. 2016, 138, 7840.
doi: 10.1021/jacs.6b04364 |
[39] |
Singha, S.; Patra, T.; Daniliuc, C. G.; Glorius, F. J. Am. Chem. Soc. 2018, 140, 3551.
doi: 10.1021/jacs.8b00868 |
[40] |
Ding, Y. L.; Zhao, Y. L.; Niu, S. S.; Wu, P.; Cheng, Y. J. Org. Chem. 2020, 85, 612.
doi: 10.1021/acs.joc.9b02693 |
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