Chin. J. Org. Chem. ›› 2013, Vol. 33 ›› Issue (9): 1851-1873.DOI: 10.6023/cjoc201301073 Previous Articles Next Articles
Reviews
赵树春a,b, 于奕峰a,b,c, 张越a,b,c
收稿日期:2013-01-28
修回日期:2013-04-13
发布日期:2013-04-17
通讯作者:
张越
E-mail:yuezhang@hebust.edu.cn
Zhao Shuchuna,b, Yu Yifenga,b,c, Zhang Yuea,b,c
Received:2013-01-28
Revised:2013-04-13
Published:2013-04-17
Share
Zhao Shuchun, Yu Yifeng, Zhang Yue. Recent Advances in the Synthesis of Stilbenes[J]. Chin. J. Org. Chem., 2013, 33(9): 1851-1873.
| [1] Si, J.-Y. Nat. Prod. Res. Dev. 1994, 6, 71 (in Chinese).(斯建勇, 天然产物研究与开发, 1994, 6, 71.)[2] Long, S.-H. M.S. Thesis, Jiangnan University, Wuxi, 2008 (in Chinese).(龙苏华, 硕士论文, 江南大学, 无锡, 2008.) [3] Wang, S.-S.; Zhao, W.-J.; Liu, Z.-G. World Notes Plant Med. 2001, 16, 9 (in Chinese).(王世盛, 刘伟杰, 刘志广, 国外医药·植物药分册, 2001, 16, 9.) [4] Niu, P.-Q.; Guo, C.-Y. Herald Med. 2006, 25, 524 (in Chinese).(牛培勤, 郭传勇, 医药导报, 2006, 25, 524.) [5] Chen, G. H.; Webster, J. M.; Li, J. X.; Hu, K. J.; Zhu, J. WO 042231, 2001 [Chem. Abstr. 2001, 135, 45986]. [6] Jang, M.; Cai, L.; Udeani, G. O.; Slowing, K. V.; Thomas, C. F.; Beecher, C. W.; Fong, H. H.; Farnsworth, N. R.; Kinghorn, A. D.; Mehta, R. G.; Moon, R. C.; Pezzuto, J. M. Science 1997, 275, 218. [7] Liu, S.-X.; Cheng, L.-Y. Food Sci. Technol. 2005, (2), 96 (in Chinese).(刘树兴, 程丽英, 食品科技, 2005, (2), 96.) [8] Yang, Q. Org.-Fluorine Ind. 1995, 2, 6 (in Chinese).(杨青, 有机氟工业, 1995, 2, 6.) [9] Spells, D. J.; Lindsey, C.; Dalton, L. R. Liquid Cryst. 2002, 29, 1529. [10] Suzuki, Y.; Sugiyama, Y.; Mitamura, S.; Nishiama, T.; Takesono, T. JP 04230739, 1992[Chem. Abstr. 1993, 118, 112591]. [11] Diemer, V.; Chaumeil, H.; Defoin, A.; Carre, C. Synthesis 2007, 3333. [12] Xu, H.-Y.; Wu, L.; Hu, L. Spectrosc. Spect. Anal. 2008, 28, 2356 (in Chinese).(徐洪耀, 吴蕾, 胡蕾, 光谱学与光谱分析, 2008, 28, 2356.) [13] Xia, T.; Meng, Q.-H.; Geng, Y.-C.; Zhang, W.-B.; Huang, D.-Y. Dyest. Color. 2007, 44, 37 (in Chinese).(夏天, 孟庆华, 耿彦朝, 张万斌, 黄德音, 染料与染色, 2007, 44, 37.) [14] Ge, G.-Z. Text. Aux. 2010, 27, 4 (in Chinese).(葛广周, 印染助剂, 2010, 27, 4.) [15] Becker, K. B. Synthesis 1983, 341. [16] Franz, R. A.; Montgomery, P. D.; Gebhart, H. J. Jr. US 3739038, 1973[Chem. Abstr. 1973, 79, 42121]. [17] Allum, K. G.; Howell, I. V.; Pitkethly, R. C. GB 1378151, 1974 [Chem. Abstr. 1974, 82, 125043]. [18] Blum, J.; Biger, S. Tetrahedron Lett. 1970, 21, 1825. [19] Bance, S.; Barber, H. J.; Woolman, A. M. J. Chem. Soc. 1943, 1. [20] Levin, G.; Jagur-Grodzinski, J.; Szwarc, M. J. Org. Chem. 1970, 35, 1702. [21] Irvine, J. C.; Weir, J. Transactions 1907, 91, 1384. [22] Yong, W. R.; Aviram, A.; Cox, R. J. J. Am. Chem. Soc. 1972, 94, 3976. [23] Drefahl, G.; Plotner, G. Chem. Ber. 1958, 91, 1274. [24] Li, Y.-Q. Ph.D. Dissertation, Dalian University of Technology, Dalian, 2006 (in Chinese).(李悦青, 博士论文, 大连理工大学, 大连, 2006.) [25] Reetz, M. T.; Plachky, M. Synthesis 1976, 199. [26] Mathai, I. M.; Schug, K.; Miller, S. I. J. Org. Chem. 1970, 35, 1733. [27] Corey, E. J.; Winter, A. E. J. Am. Chem. Soc. 1963, 85, 2677. [28] Sonnet, P. E. Tetrahedron 1980, 36, 557. [29] Mitchell, R. H. Tetrahedron Lett. 1973, 44, 4395. [30] Howard, L. B.; Hilbert, G. E.; Wiebe, R.; Gaddy, V. L. J. Am. Chem. Soc. 1932, 54, 3628. [31] Binkley, R. W. J. Org. Chem. 1969, 34, 931. [32] Green, A. G.; Baddiley, J. J. Chem. Soc. 1908, 93, 1721. [33] Montgomery, P. D.; Moore, R. N.; Knox, W. R. US 3965206, 1976[Chem. Abstr. 1976, 85, 123540]. [34] Tremont, S. J.; Williamson, A. N.; Solodar, A. J. US 4268704, 1981[Chem. Abstr. 1981, 95, 80442]. [35] Liu, K. H. D.; Masuda, A.; Yamazaki, Y. Tetrahedron Lett. 1975, 34, 3007. [36] Onagi, H.; Carrozzini, B.; Cascarano, G. L.; Easton, C. J.; Edwards, A. J.; Lincoln, S. F.; Rae, A. D. Chem. Eur. J. 2003, 9, 5971. [37] Cieslinski, M. M.; Steel, P. J.; Lincoln, S. F.; Easton, C. J. Supramol. Chem. 2006, 18, 529. [38] Hauser, C. R.; Brasen, W. R.; Skell, P. S.; Kantor, S. W.; Brodhag, A. E. J. Am. Chem. Soc. 1956, 78, 1653. [39] Okazaki, M.; Mita, R. JP 49110656, 1974[Chem. Abstr. 1975, 83, 27837]. [40] Feuer, H.; Friedman, H. J. Org. Chem. 1975, 40, 187. [41] Wood, J. H.; Bacon, J. A.; Throckmorton, W. H.; Turner, G. P. J. Am. Chem. Soc. 1941, 63, 1334. [42] Sishido, K.; Takeda, Y.; Nozaki, H. J. Org. Chem. 1962, 27, 2411. [43] Ogata, Y.; Nakamura, H. J. Org. Chem. 1956, 21, 1170. [44] Perkin, W. H. J. Chem. Soc. 1877, 31, 388. [45] Späth, E.; Kromp, K. Chem. Ber. 1941, 74, 867. [46] Soliadié, G.; Pastural-Jacope, Y.; Maignan, J. Tetrahedron 2003, 59, 3315. [47] Zhu, Y.-S.; Luo, S.-N.; Shen, Y.-J.; Yu, H.-X.; Chen, B.; Zhang, L.-G. Chin. J. Org. Chem. 2006, 26, 958 (in Chinese).(朱玉松, 罗世能, 沈永嘉, 俞惠新, 陈波, 张来国, 有机化学, 2006, 26, 958.) [48] Sinha, A. K.; Kumar, V.; Sharma, A.; Sharma A.; Kumar, R. Tetrahedron 2007, 63, 11070. [49] Du, J.-L.; Zhou, Y.; Xiao, C.-F. Fine Chem. 2009, 26, 580 (in Chinese).(都建立, 邹永, 肖春芬, 精细化工, 2009, 26, 580.) [50] Li, G. X.; Zou, Y.; Zhang, X. J. J. Chem. Res. 2007, 11, 657. [51] Hou, B.-B.; Feng, J.-J.; Yang, S.-W.; Ao, G.-Z. Chem. Reag. 2011, 33, 1141 (in Chinese).(侯丙波, 冯江江, 杨圣伟, 敖桂珍, 化学试剂, 2011, 33, 1141.) [52] Ao, G. Z.; Hou, B. B.; Cao, Y.; Yang, S. W.; Feng, J. J. CN 102180773, 2011[Chem. Abstr. 2011, 155, 431581]. [53] Xiao, C.-F.; Sun, H.-Y.; Chen, Y.; Lv, Z.-L.; Zou, Y. Nat. Prod. Res. Dev. 2010, 22, 548 (in Chinese).(肖春芬, 孙洪宜, 陈煜, 吕泽良, 邹永, 天然产物研究与开发, 2010, 22, 548.) [54] Sun, H.-Y.; Xiao, C.-F.; Wei, W.; Chen, Y.; Lv, Z.-L.; Zou, Y. Chin. J. Org. Chem. 2010, 30, 1574 (in Chinese).(孙洪宜, 肖春芬, 魏文, 陈煜, 吕泽良, 邹永, 有机化学, 2010, 30, 1574.) [55] Xiao, C. F.; Zou, Y.; Du, J. L.; Sun, H. Y.; Liu, X. K. Synth. Commun. 2012, 42, 1243. [56] Heck, R. F. J. Am. Chem. Soc. 1968, 90, 5518. [57] Guiso, M.; Marra, C.; Farina, A. Tetrahedron Lett. 2002, 43, 597. [58] Botella, L.; Nájera, C. Tetrahedron 2004, 60, 5563. [59] Mu, F.; Hamel, E.; Lee, D. J.; Pryor, D. E.; Cushman, M. J. Med. Chem. 2003, 46, 1670. [60] Leadbeater, N. E.; Tominack, B. J. Tetrahedron Lett. 2003, 44, 8653. [61] Yan, Q.-Q.; Liu, Y.-X.; Li, Z.-Q.; Yang, Y.; Wang, W.-F. Chem. Reag. 2011, 33, 852 (in Chinese).(闫起强, 刘蕴秀, 李志强, 杨琰, 王文峰, 化学试剂, 2011, 33, 852.) [62] Wehrli, C. EP 2468706, 2012[Chem. Abstr. 2012, 157, 104501]. [63] Andrus, M. B.; Liu, J.; Meredith, E. L.; Nartey, E. Tetrahedron Lett. 2003, 44, 4819. [64] Andrus, M. B.; Liu, J. Tetrahedron Lett. 2006, 47, 5811. [65] Li, Y.-Z.; Li, N.; Fu, B.; Zhang, S.-S.; Qin, Z.-H. Chem. Reag. 2006, 28, 363 (in Chinese).(李印钊, 李楠, 付滨, 张曙生, 覃兆海, 化学试剂, 2006, 28, 363.) [66] Myers, A. G.; Tanaka, D.; Mannion, M. R. J. Am. Chem. Soc. 2002, 124, 11250. [67] Jeffery, T.; Ferber, B. Tetrahedron Lett. 2003, 44, 193. [68] Farina, A.; Ferranti C.; Marra, C. Nat. Prod. Res. 2006, 20, 247. [69] Albert, S.; Horbach, R.; Deising, H. B.; Siewert, B.; Csuk, R. Bioorg. Med. Chem. 2011, 19, 5155. [70] Csuk, R.; Albert, S.; Siewert, B.; Schwarz, S. Eur. J. Med. Chem. 2012, 54, 669. [71] Farina, A.; Ferranti, C.; Marra, C.; Guiso, M.; Norcia, G. Nat. Prod. Res. 2007, 21, 564. [72] Moro, A. V.; Cardoso, F. S. P.; Correia, C. R. D. Tetrahedron Lett. 2008, 49, 5668. [73] Yamada, Y. M. A.; Takeda, K.; Takahashi, H.; Ikegami, S. Tetrahedron 2004, 60, 4097. [74] Su, X.-Y.; Wu, L.; Xu, H.-Y. Chin. J. Appl. Chem. 2008, 25, 1487 (in Chinese).(苏新艳, 吴蕾, 徐洪耀, 应用化学, 2008, 25, 1487.) [75] Liu, Y.; Liu, W. CN 102276426, 2011[Chem. Abstr. 2011, 156, 74028]. [76] Morales-Serna, J. A.; Zúñiga-Martínez, A.; Salmón, M.; Gaviño, R.; Cárdenas, J. Synthesis 2012, 446. [77] Yu, K. L.; Deshpande, M. S.; Vyas, D. M. Tetrahedron Lett. 1994, 35, 8919. [78] Tamura, M.; Kochi, J. K. J. Am. Chem. Soc. 1971, 93, 1487. [79] Dohle, W.; Kopp, F.; Cahiez, G.; Knochel, P. Synlett 2001, 1901. [80] Christofers, J. Synlett 2001, 723. [81] Shirakawa, E.; Yamagami, T.; Kimura, T.; Yamaguchi, S.; Hayashi, T. J. Am. Chem. Soc. 2005, 127, 17164. [82] Sherry, B. D.; Fürstner, A. Acc. Chem. Res. 2008, 41, 1500. [83] Bézier, D.; Sortais, J. B.; Darcel, C. Adv. Synth. Catal. 2013, 355, 19. [84] Tamao, K.; Sumitani, K.; Kumada, M. J. Am. Chem. Soc. 1972, 94, 4374. [85] Corriu, R. J. P.; Masse, J. P. J. Chem. Soc., Chem. Commun. 1972, 3, 144. [86] Wenkert, E.; Michelotti, E. L.; Swindell, C. S.; Tingoli, M. J. Org. Chem. 1984, 49, 4894. [87] Okamura, H.; Miura, M.; Kodugi, K.; Takei, H. Tetrahedron Lett. 1980, 21, 87. [88] Xi, Z. X.; Liu, B.; Chen, W. Z. J. Org. Chem. 2008, 73, 3954. [89] Harter, R.; Lemke, U.; Radspieler, A. WO 023740, 2005[Chem. Abstr. 2005, 142, 297871]. [90] Chen, Y.-P.; Lei, T.-K. Chin. J. Pharm. 2000, 31, 334 (in Chinese).(陈毅平, 雷同康, 中国医药工业杂志, 2000, 31, 334.) [91] Moreno-Manas, M.; Pleixats, R. An. Quim. 1985, 81, 157. [92] Lonsky, L.; Lonsky, W.; kratzl, K.; Falkehag, I. Monatsh. Chem. 1976, 107, 685. [93] Steynberg, J. P.; Ferreria, D.; Roux, D. G. J. Chem. Soc., Perkin Trans. 1 1987, 1705. [94] Ali, M. A.; Kondo, K.; Tsuda, Y. Chem. Pharm. Bull. 1992, 40, 1130. [95] Li, X.-G.; Wang, S.-Y.; Li, C.-R.; Li, S.-X. China Food Addit. 2002, (5), 25 (in Chinese).(李晓光, 王三永, 李春荣, 李韶雄, 中国食品添加剂, 2002, (5), 25.) [96] Yan, R.-A.; Ding, L.-G.; Li, A.-J.; Feng, J.-L.; Fu, Y.-P. Food Fermen. Ind. 2006, 32, 95 (in Chinese).(宴日安, 丁刘刚, 李爱军, 冯锦玲, 傅玉萍, 食品与发酵工业, 2006, 32, 95.) [97] Roberti, M.; Pizzirani, D.; Simoni, D.; Rondanin, R.; Baruchello, R.; Bonora, C.; Buscemi, F.; Grimaudo, S.; Tolomeo, M. J. Med. Chem. 2003, 46, 3546. [98] Gabriele, B.; Benabdelkamel, H.; Plastina, P.; Fazio, A.; Sindona, G.; Di Donna, L. Synthesis 2008, 2953. [99] Alonso, F.; Riente, P.; Yus, M. Tetrahedron Lett. 2009, 50, 3070. [100] Alonso, F.; Riente, P.; Yus, M. Eur. J. Org. Chem. 2009, 34, 6034. [101] McNulty, J.; Das, P. Eur. J. Org. Chem. 2009, 24, 4031. [102] Gray, E. E.; Rabenold, L. E.; Goess, B. C. Tetrahedron Lett. 2011, 52, 6177. [103] Gu, Y. M.S. Thesis, East China University of Science and Technology, Shanghai, 2012 (in Chinese).(顾烨, 硕士论文, 华东理工大学, 上海, 2012.) [104] Bestmann, H. J.; Seng, F. Angew. Chem., Int. Ed. 1963, 2, 393. [105] Bestmann, H. J. Angew. Chem., Int. Ed. 1965, 4, 830. [106] Dong, D. J.; Li, H. H.; Tian, S. K. J. Am. Chem. Soc. 2010, 132, 5018. [107] Fang, F.; Li, Y.; Tian, S. K. Eur. J. Org. Chem. 2011, 6, 1084. [108] Dong, D. J.; Li, Y.; Wang, J. Q.; Tian, S. K. Chem. Commun. 2011, 47, 2158. [109] Thakkar, K.; Geahlen, R. L.; Cushman, M. J. Med. Chem. 1993, 36, 2950. [110] Feng, Y. B.; Wang, L.; Zhao, Z. Z. Chin. Chem. Lett. 1998, 9, 1003. [111] Zhuo, G.-L. Shen, Z.-L.; Jia, X.-Z. Chin. J. Med. Chem. 2002, 12, 152 (in Chinese).(卓广澜, 沈振陆, 姜玄珍, 中国药物化学杂志, 2002, 12, 152.) [112] Andrus, M.; Meredith, E. WO 060774, 2001[Chem. Abstr. 2001, 135, 180660]. [113] Takaya, Y.; Terashima, K.; Ito, J.; He, Y. H.; Tateoka, M.; Yamaguchi, N.; Niwa, M. Tetrahedron 2005, 61, 10285. [114] Wang, Z.-Y.; Ma, Z.; Li, Q.; Shen, Z.-R. Chin. J. Pharm. 2003, 34, 428 (in Chinese).(王尊元, 马臻, 李强, 沈正荣, 中国医药工业杂志, 2003, 34, 428.) [115] Wang, S.-J.; Zhao, W.-J.; Liu, Z.-G.; Wang, X.-Q. Chin. J. Med. Chem. 2004, 14, 91 (in Chinese).(王世盛, 赵伟杰, 刘志广, 王夏青, 中国药物化学杂志, 2004, 14, 91.) [116] Chen, G.-L.; Shan, W.; Xu, Y.; Dong, J.-H.; Zhang, B.-F.; Ji, Z.-Z. J. Shenyang Pharm. Univ. 2004, 21, 261 (in Chinese).(陈国良, 单伟, 徐颖, 董金华, 张宝凤, 计志忠, 沈阳药科大学学报, 2004, 21, 261.) [117] Liu, P.; Li, J.-J.; Cheng, M.-S. Chin. J. Med. Chem. 2008, 18, 424 (in Chinese).(刘鹏, 李家杰, 程卯生, 中国药物化学杂志, 2008, 18, 424.) [118] Hou, J.; Wang, G.-P.; Zou, Q. Chin. J. Pharm. 2008, 39, 1 (in Chinese).(侯建, 王国平, 邹强, 中国医药工业杂志, 2008, 39, 1.) [119] Jungong, C. S.; Novikov, A. V. Synth. Commun. 2012, 42, 3589. [120] Chen, G. H.; Li, J. X.; Liu, W.; Webster, J. M. WO 031117, 2004[Chem. Abstr. 2004, 140, 321106]. [121] Gao, J. G.; Zhang, Y.; Zheng, H. T.; Wang, C. F.; Liu, H. X.; Zhao, S. C. Adv. Mater. Res. 2011, 236～238, 2378. [122] Zhang, Y.; Zhang, Y. Y.; Yu, C. J.; Wang, C. F.; Zhao, S. C. Adv. Mater. Res. 2012, 479～481, 833. [123] Zhang, Y.; Zhao, S. C.; Zhang, Y. Y. CN 101633606, 2009[Chem. Abstr. 2010, 152, 238601]. [124] Zhang, Y.; Zhao, S. C. CN 101830764, 2010[Chem. Abstr. 2010, 153, 456312]. [125] Zhang, Y.; Zhao, S. C. CN 101838173, 2010[Chem. Abstr. 2010, 153, 480702]. [126] Li, C.-R.; Xu, Z.-L.; Wang, H.; Wang, S.-Y. China Food Addit. 2007, (3), 54 (in Chinese).(李春荣, 许忠良, 王辉, 王三永, 中国食品添加剂, 2007, (3), 54.) [127] Li, X.-X.; Yan, R.-A.; Duan, H.-Y. Fine Chem. 2011, 28, 475 (in Chinese).(李晓霞, 晏日安, 段翰英, 精细化工, 2011, 28, 475.) [128] Lee, H. S.; Lee, B. W.; Kim, M. R.; Jun, J. G. Bull. Korean Chem. Soc. 2010, 31, 971. [129] McMurry J. E.; Fleming, M. P. J. Am. Chem. Soc. 1974, 96, 4708. [130] Mukaiyama, T.; Sato, T.; Hanna, J. Chem. Lett. 1973, 10, 1041. [131] Mohammad, A. A.; Kaolu, K.; Yoshisuke, T. Chem. Pharm. Bull. 1992, 40, 1130. [132] Ding, N. M.S. Thesis, Ocean University of China, Qingdao, 2004 (in Chinese).(丁宁, 硕士论文, 中国海洋大学, 青岛, 2004.) [133] Stuhr-Hansen, N. Tetrahedron Lett. 2005, 46, 5491. [134] Manish, V. D.; Mythili, K.; Aruna, G. K.; Usha, P.; Subrata, C.; Sharmila, B. Appl. Radiat. Isot. 2011, 69, 996. [135] Miyaura, N.; Suzuki, A. J. Chem. Soc. 1979, 19, 866. [136] Eddarir, S.; Abdelhadi, Z.; Rolando, C. Tetrahedron Lett. 2001, 42, 9127. [137] Wang, Z. X.; Zhang, X. J.; Zhou, Y.; Zou, Y. J. Chin. Pharm. Sci. 2005, 14, 204. [138] Koji, O.; Ryusuke, N.; Yumiko, F.; Toshihiro, H.; Yoshi-hiro, M.; Yukio, N.; Kazuo, O.; Yasuyo, S.; Yukio, A.; Ta-kashi, T. J. Med. Chem. 1998, 41, 3022. [139] Tana, N.; Sasson, Y.; Chidambaram, M. Appl. Catal., A 2008, 350, 217. [140] Huang, X.; Wang, Y. G.; Chen, Z. C. New Organic Synthetic Chemistry, Chemical Industry Press, Beijing, 2003, p. 68. [141] Wang, W. F.; Zou, J.; Hua, Y. N.; Liu, H. L. CN 1994991, 2006[Chem. Abstr. 2006, 147, 211671]. [142] Alonso, E.; Ramon, D. J.; Yus, M. J. Org. Chem. 1997, 62, 417. [143] Zhang, X. J.; Zhu, J.; Xiong, X. Y.; Zou, Y.; Lin, H. Z. J. Chin. Pharm. Sci. 2004, 13, 10. [144] Zou, Y.; Zhang, X. J.; Lin, H. Z. CN 1539805, 2004[Chem. Abstr. 2004, 143, 153145]. [145] Jiang, Y. CN 102050702, 2011[Chem. Abstr. 2011, 154, 565057]. [146] Ren, Y.-R.; Jiang, Y. Chin. J. Pharm. 2012, 43, 656 (in Chinese).(任彦荣, 蒋勇, 中国医药工业杂志, 2012, 43, 656.) [147] Julia, M.; Paris, J. M. Tetrahedron Lett. 1973, 49, 4833. [148] Alonso, D. A.; Nájera, C.; Varea, M. Tetrahedron Lett. 2004, 45, 573. [149] Wang, J. X.; Fu, Y.; Hu, Y. L. Angew. Chem., Int. Ed. 2002, 41, 2757. [150] Xu, L.-Y. M.S. Thesis, Northwest Normal University, Lanzhou, 2009 (in Chinese).(徐雷云, 硕士论文, 西北师范大学, 兰州, 2009.) [151] Kabalka, G. W.; Wu, Z.; Ju, Y. Tetrahedron Lett. 2001, 42, 4759. [152] Chang, S.; Na, Y.; Shin, H. J.; Choi, E.; Jeong, L. S. Tetrahedron Lett. 2002, 43, 7445. [153] Ferré-Filmon, K.; Delaude, L.; Demonceau, A.; Noels, A. F. Eur. J. Org. Chem. 2005, 15, 3319. |
| [1] | Penghui Li, Qingyang Xie, Fuxian Wan, Yuanhong Zhang, Lin Jiang. Synthesis and Fungicidal Activity of Novel Substituted Pyrimidine-5-carboxamides Bearing Cyclopropyl Moiety [J]. Chinese Journal of Organic Chemistry, 2024, 44(2): 650-656. |
| [2] | Fakai Zou, Nengzhong Wang, Hui Yao, Hui Wang, Mingguo Liu, Nianyu Huang. Regio- and Stereo-selective Synthesis of 1β-/3R-Aryl Thiosugar [J]. Chinese Journal of Organic Chemistry, 2024, 44(2): 593-604. |
| [3] | Luyao Li, Zhongwen He, Zhenguo Zhang, Zhenhua Jia, Teck-Peng Loh. Application of Triaryl Carbenium in Organic Synthesis [J]. Chinese Journal of Organic Chemistry, 2024, 44(2): 421-437. |
| [4] | Qinggang Mei, Qinghan Li. Recent Progress of Visible Light-Induced the Synthesis of C(3) (Hetero)arylthio Indole Compounds [J]. Chinese Journal of Organic Chemistry, 2024, 44(2): 398-408. |
| [5] | Weiqing Yang, Yanbing Ge, Yuanyuan Chen, Ping Liu, Haiyan Fu, Menglin Ma. Design and Synthesis of Fluorescent 1,8-Napthalimide Derivatives and Their Identification of Cysteine [J]. Chinese Journal of Organic Chemistry, 2024, 44(1): 180-194. |
| [6] | Qianfan Zhao, Yongzheng Chen, Shiming Zhang. Application and Mechanism Study of Carbon-Based Metal-Free Catalysts in Organic Synthesis [J]. Chinese Journal of Organic Chemistry, 2024, 44(1): 137-147. |
| [7] | Shan Chen, Zhilin Chen, Qiong Hu, Yanshuang Meng, Yue Huang, Pingfang Tao, Liru Lu, Guobao Huang. Recognition of Bis-thiourea Tweezers to Neutral Molecules in Non-Polar Solvent [J]. Chinese Journal of Organic Chemistry, 2024, 44(1): 277-281. |
| [8] | Huakun Wang, Xiaolong Ren, Yining Xuan. Study of the Halide Salt Catalyzed [3＋2] Cycloaddition of α,β-Epoxy Carboxylate with Isocyanate [J]. Chinese Journal of Organic Chemistry, 2024, 44(1): 251-258. |
| [9] | Yukun Jin, Baoyi Ren, Fushun Liang. Visible Light-Mediated Selective C—F Bond Cleavage of Trifluoromethyl Groups and Its Application in Synthesizing gem-Difluoro-Containing Compounds [J]. Chinese Journal of Organic Chemistry, 2024, 44(1): 85-110. |
| [10] | Cuiyun Ma, Hailan Luo, Fuhua Zhang, Dan Guo, Shuxing Chen, Fei Wang. Green Biosynthesis, Photophysical Properties and Application of 3-Pyrrolyl BODIPY [J]. Chinese Journal of Organic Chemistry, 2024, 44(1): 216-223. |
| [11] | Bozhen Wang, Jie Zhang, Chunhui Nian, Mingming Jin, Miaomiao Kong, Wulan Li, Wenfei He, Jianzhang Wu. Synthesis and Antitumor Activity of 3,4-Dichlorophenyl Amides [J]. Chinese Journal of Organic Chemistry, 2024, 44(1): 232-241. |
| [12] | Shihang Yu, Jiawei Liu, Biyu An, Qinghua Bian, Min Wang, Jiangchun Zhong. Asymmetric Synthesis of the Contact Sex Pheromone of Neoclytus acuminatus acuminatus (Fabricius) [J]. Chinese Journal of Organic Chemistry, 2024, 44(1): 301-308. |
| [13] | Yang Li, Jinding Yuan, Di Zhao. Deep Eutectic Solvent of 1,3-Dimethylurea/L-(+)-Tartaric Acid for the Green Synthesis of (E)-2-Styrylquinoline-3-carboxylic Acid Derivatives [J]. Chinese Journal of Organic Chemistry, 2023, 43(9): 3268-3276. |
| [14] | Dandan Sui, Nannan Cen, Ruoqu Gong, Yang Chen, Wenbo Chen. Supporting-Electrolyte-Free Electrochemical Synthesis of Trifluoromethylated Oxindoles in Continuous Flow [J]. Chinese Journal of Organic Chemistry, 2023, 43(9): 3239-3245. |
| [15] | Ruixia Cao, Yuping Jia. Synthesis and Biological Activity of Novel Pyrrolo[2,3-d]pyrimidine Derivatives Containing Coumarin [J]. Chinese Journal of Organic Chemistry, 2023, 43(9): 3304-3311. |
| Viewed | ||||||
|
Full text |
|
|||||
|
Abstract |
|
|||||
