综述与进展

三联苯类化合物合成方法的研究进展

  • 石巍 ,
  • 俞婷婷 ,
  • 崔冬梅
展开
  • 浙江工业大学药学院 杭州 310014

收稿日期: 2014-09-05

  修回日期: 2014-10-16

  网络出版日期: 2014-10-30

基金资助

浙江省自然科学基金(No. Y4100558)资助项目.

Advances in the Synthetic Methods of Terphenyls

  • Shi Wei ,
  • Yu Tingting ,
  • Cui Dongmei
Expand
  • College of Pharmaceutical Science, Zhejiang University of Technology, Hangzhou 310014

Received date: 2014-09-05

  Revised date: 2014-10-16

  Online published: 2014-10-30

Supported by

Project supported by the Natural Science Foundation of Zhejiang Province (No. Y4100558).

摘要

三联苯类化合物具有免疫抑制、抗氧化、神经保护、细胞毒以及抗血栓等多种生物活性, 同时在液晶材料方面也有着广泛的应用. 因此该类化合物的合成备受人们的关注. 以偶联、环合、脱氢等反应进行分类, 综述了近年合成该类化合物的方法. 通过该角度的综述, 我们希望能为设计出更好的合成方法带来启示.

本文引用格式

石巍 , 俞婷婷 , 崔冬梅 . 三联苯类化合物合成方法的研究进展[J]. 有机化学, 2015 , 35(2) : 362 -372 . DOI: 10.6023/cjoc201409007

Abstract

Terphenyl derivatives possess various biological activities, such as immunosuppressants, antioxidants, neuroprotective activity, cytotoxic activity, and antithrombotic activity, and they are also widely used in liquid crystal materials. Significant effort has been devoted to the synthesis of such compounds. Classified into coupling reaction, cycloaddition, dehydrogenation and other methods, this review provides a summary of recently developed methods for the preparation of terphenyls.

参考文献

[1] Liu, J. K. Chem. Rev. 2006, 106, 2209.
[2] Kamigauchi, T.; Sakazaki, R.; Nagashima, K.; Kawamura, Y.; Yasuda, Y.; Matsushima, K.; Tani, H.; Takahashi, Y.; Ishii, K.; Suzuki, R.; Koizumi, K.; Nakai, H.; Ikenishi, Y.; Terui, Y. J. Antibiot. 1998, 51, 445.
[3] (a) Yun, B. S.; Lee, I. K.; Kim, J. P.; Yoo, I. D. J. Antibiot. 2000, 53, 114.
(b) Quang, D. N.; Hashimoto, T.; Nukada, M.; Yamamoto, I.; Tanaka, M.; Asakawa, Y. Planta Med. 2003, 69, 1063.
[4] Holzapfel, M.; Kilpert, C.; Steglich, W. Liebigs Ann. Chem. 1989, 797.
[5] Stead, P.; Affleck, K.; Sidebottom, P. J.; Taylor, N. L.; Drake, C.; Todd, M.; Jowett, A.; Webb, G. J. Antibiot. 1999, 52, 89.
[6] (a) Miyamae, T.; Hashizume, H.; Ogawa, T.; Okayama, T.; Nukui, E.; Oshima, K.; Morikawa, T.; Hagiwara, M. Arzneim. Forsch.1997, 47, 13.
(b) Hongou, K.; Miyamae, T.; Hashizume, H.; Oshima, K.; Ogawa, T.; Hongou, T.; Morikawa, T.; Hagiwara, M. Arzneim. Forsch.1997, 47, 1104.
[7] Hu, G.; Tang, H.; Xu, S.-Y. Funct. Mater. 1999, 30, 665 (in Chinese). (胡刚, 唐洪, 徐寿颐, 功能材料, 1999, 30, 665.)
[8] Li, W.-Y.; Zhao, D.-M.; Xiong, X.-Q.; Ma, Q.-Q.; Cheng, M.-S., Chin. J. Org. Chem. 2011, 31, 784 (in Chinese). (李文燕, 赵冬梅, 熊绪琼, 马倩倩, 程卯生, 有机化学, 2011, 31, 784.)
[9] (a) Liang, Y.; Li, J.-H. Chin. J. Org. Chem. 2005, 25, 147 (in Chinese). (梁云, 李金恒, 有机化学, 2005, 25, 147.)
(b) Li, Z.-K.; Wu, Z.-Q.; Deng, H.; Zhou, X.-G. Chin. J. Org. Chem. 2013, 33, 760 (in Chinese). (李正凯, 吴之清, 邓杭, 周向葛, 有机化学, 2013, 33, 760.)
[10] Hassan, J.; Hathroubi, C.; Gozzi, C.; Lemaire, M. Tetrahedron 2001, 57, 7845.
[11] Liu, N.; Liu, C.; Jin, Z.-L., Chin. J. Org. Chem. 2012, 32, 860 (in Chinese). (刘宁, 刘春, 金子林, 有机化学, 2012, 32, 860.)
[12] Zhang, Z.; Zhang, G.-X.; Li, S.-H.; Liu, C.-Y.; Bai, X.-F.; Zhao, Y.-L.; Wang, J.-Y. Chem. Adhesion 2014, 36, 132 (in Chinese). (张智, 张广鑫, 李淑辉, 刘传玉, 白雪峰, 赵毅磊, 王洁莹, 化学与黏合, 2014, 36, 132.)
[13] Li, Z. H.; Wong, M. S.; Tao, Y. Tetrahedron 2005, 61, 5277.
[14] Bolligera, J. L.; Frecha, C. M. Adv. Synth. Catal. 2010, 352, 1075.
[15] Liu, H. Y.; Liu, H. L.; Li, R. X.; Chen, H. Tetrahedron Lett. 2014, 55, 415.
[16] Borhade, S. R.; Waghmode, S. B. Beilstein J. Org. Chem. 2011, 7, 310.
[17] Mandali, P. K.; Chand, D. K. Catal. Commun. 2013, 31, 16.
[18] Ali, I.; Siyo, B.; Hassan, Z.; Malik, I.; Ullah, I.; Ali, A.; Nawaz, M.; Iqbal, J.; Patonay, T.; Villinger, A.; Langer, P. J. Fluorine Chem. 2013, 145, 18.
[19] Yajima, A.; Urao, S.; Yoshioka, Y.; Abe, N.; Katsuta, R.; Nukada, T. Tetrahedron Lett. 2013, 54, 4986.
[20] Peters, M.; Trobe, M.; Tan, H.; Kleineweischede, R.; Breinbauer, R. Chem. Eur. J. 2013, 19, 2442.
[21] Wang, D.-P.; Zhang, X.-D.; Liang, Y.; Li, J.-H., Chin. J. Org. Chem. 2006, 26, 19 (in Chinese). (王德平, 张旭东, 梁云, 李金恒, 有机化学, 2006, 26, 19.)
[22] Corsico, E. F.; Rossi, R. A. Synlet 2000, 230.
[23] Li, J. H.; Liang, Y.; Wang, D. P.; Liu, W. J.; Xie, Y. X.; Yin, D. L. J. Org. Chem. 2005, 70, 2832.
[24] (a) Qiu, D.; Meng, H.; Jin, L.; Wang, S.; Tang, S. B.; Wang, X.; Mo, F. Y.; Zhang, Y.; Wang, J. B. Angew. Chem., Int. Ed. 2013, 52, 11581.
(b) Qiu, D.; Wang, S.; Tang, S. B.; Meng, H.; Jin, L.; Mo, F. Y.; Zhang Y.; Wang, J. B. J. Org. Chem. 2014, 79, 1979.
[25] Yoshikai, N.; Matsuda, H.; Nakamura, E. J. Am. Chem. Soc. 2009, 131, 9590.
[26] Jin, Z.; Li, Y. J.; Ma, Y. Q.; Qiu, L. L.; Fang, J. X. Chem. Eur. J. 2012, 18, 446.
[27] (a) Styring, P.; Grindon, C.; Fisher, C. M. Catal. Lett. 2001, 77, 219.
(b) Tsai, F. Y.; Lin, B. N.; Chen, M. J.; Mou, C. Y.; Liu, S. T. Tetrahedron 2007, 63, 4304.
[28] Ju, J. H.; Nam, H.; Jung, H. M.; Lee, S. Tetrahedron Lett. 2006, 47, 8673.
[29] Shi, S. Y.; Zhang, Y. H. J. Org. Chem. 2007, 72, 5927.
[30] Ranu, B. C.; Dey, R.; Chattopadhyay, K. Tetrahedron Lett. 2008, 9, 3430.
[31] Shao, Z.-Q.; Li, X.; Chang, H.-H.; Wei, W.-L. Chem. Online 2013, 76, 704 (in Chinese). (邵忠奇, 李兴, 常宏宏, 魏文珑, 化学通报, 2013, 76, 704.)
[32] Dai, C. Y.; Fu, G. C. J. Am. Chem. Soc. 2001, 123, 2719.
[33] Xi, Z. X.; Zhou, Y. B.; Chen, W. Z. J. Org. Chem. 2008, 73, 8497.
[34] Liu, N.; Wang, L.; Wang, Z. X. Chem. Commun. 2011, 47, 1598.
[35] Hussain, I.; Singh, T. Adv. Synth. Catal. 2014, 356, 1661.
[36] (a) Hong, W. K.; Qiu, Y. T.; Yao, Z. Y.; Wang, Z. Y.; Jiang, S. Tetrahedron Lett. 2011, 52, 4916.
(b) Liu, W.; Cao, H.; Lei, A. Angew. Chem., Int. Ed. 2010, 49, 2004.
(c) Liu, W.; Cao, H.; Xin, J.; Jin, L. Q.; Lei, A. Chem. Eur. J. 2011, 17, 3588.
[37] Zhao, H. Q.; Shen, J.; Guo, J. J.; Ye, R. J.; Zeng, H. Q. Chem. Commun. 2013, 49, 2323.
[38] Shirakawa, E.; Itoh, K.; Higashino, T.; Hayashi, T. J. Am. Chem. Soc. 2010, 132, 15537.
[39] Dewanji, A.; Murarka, S.; Curran, D. P.; Studer, A. Org. Lett. 2013, 15, 6102.
[40] Li, H. Y.; Wu, Y. Z.; Xu, X. G. J. Inorg. Organomet. Polym. 2011, 21, 827.
[41] Jasti, R.; Bhattacharjee, J.; Neaton, J. B.; Bertozzi, C. R. J. Am. Chem. Soc. 2008, 130, 17646.
[42] Lewis, F. D.; Kurth, T. L.; Hattan, C. M.; Reiter, R. C.; Stevenson, C. D. Org. Lett. 2004, 6, 1605.
[43] (a) Chopade, P. R.; Louie, J. Adv. Synth. Catal. 2006, 348, 2307.
(b) Yang, J. S.; Huang, H. H.; Lin, S. H. J. Org. Chem. 2009, 74, 3974.
(c) Gandon, V.; Aubert, C.; Malacria, M. Chem. Commun. 2006, 2209.
(d) Kotha, S.; Brahmachary, E.; Lahiri, K. Eur. J. Org. Chem. 2005, 4741.
(e) Varela, J. A.; Saa, C. Chem. Rev. 2003, 103, 3787.
(f) Rubin, S. G.; Varela, J. A.; Castedo, L.; Saa, C. Chem. Eur. J. 2008, 14, 9772.
(g) Dominguez, G.; Castells, J. P. Chem. Soc. Rev. 2011, 40, 3430.
[44] (a) Shibata, T.; Fujimoto, T.; Yokota, K.; Takagi, K. J. Am. Chem. Soc. 2004, 126, 8382.
(b) Takechi, R.; Nakaya, Y. Org. Lett. 2003, 5, 3659.
[45] (a) McDonald, F. E.; Smolentsev, V. Org. Lett. 2002, 4, 745.
(b) Tanaka, K.; Shirasaka, K. Org. Lett. 2003, 5, 4697.
(c) Tanaka, K.; Hara, H.; Nishida, G.; Hirano, M. Org. Lett. 2007, 9, 1907.
[46] (a) Deaton, K. R.; Gin, M. S. Org. Lett. 2003, 5, 2477.
(b) Bennett, M. A.; Wenger, E. Organometallics 1996, 15, 5536.
[47] Yamamoto, Y.; Arakawa, T.; Ogawa, R.; Itoh, K. J. Am. Chem. Soc. 2003, 125, 12143.
[48] (a) Gevorgyan, V.; Radhakrishnan, U.; Takeda, A.; Rubina, M.; Rubin, M.; Yamamoto, Y. J. Org. Chem. 2001, 66, 2835.
(b) Davisa, M. C.; Guenthner, A. J.; Sahagun, C. M.; Lamison, K. R.; Reams, J. T.; Mabry, J. M. Polymer 2013, 54, 6902.
[49] (a) Tsuji, H.; Yamagata, K.; Fujimoto, T.; Nakamura, E. J. Am. Chem. Soc. 2008, 130, 7792.
(b) Yoshikai, N.; Zhang, S. L.; Yamagata, K.; Tsuji, H.; Nakamura, E. J. Am. Chem. Soc. 2009, 131, 4099.
[50] Ozerov, O. V.; Ladipo, F. T.; Patrick, B. O. J. Am. Chem. Soc. 1999, 121, 7941.
[51] Wang, C.-X.; Li, X.-C.; Xu, F.; Wan, B.-S. Prog. Chem. 2010, 22, 610 (in Chinese). (王春翔, 李新成, 徐粉, 万伯顺, 化学进展, 2010, 22, 610.)
[52] Murakami, M.; Ubukata, M.; Itami, K.; Ito, Y. Angew. Chem., Int. Ed. 1998, 37, 2248.
[53] Ho, J. H.; Lin, Y. C.; Chou, L. T.; Chen, Y. N.; Liu, W. Q.; Chuang, C. L. Tetrahedron Lett. 2013, 54, 1991.
[54] Asao, N.; Aikawa, H. J. Org. Chem. 2006, 71, 5249.
[55] Zhang, L.; Liang, F. S.; Cheng, X.; Liu, Q. J. Org. Chem. 2009, 74, 899.
[56] Chang, M. Y.; Chan, C. K.; Lin, S. Y.; Wu, M. H. Tetrahedron 2013, 69, 9616.
[57] Petrova, O. V.; Mikhaleva, A. I.; Sobenina, L. N.; Trofimov, B. A. Russ. J. Org. Chem. 2010, 46, 452.
[58] Lim, C. H.; Kim, S. H.; Kim, K. H.; Kim, J. N. Tetrahedron Lett. 2013, 54, 2476.
[59] Jiang, M.; Liu, L. P.; Shi, M.; Li, Y. X. Org. Lett. 2010, 12, 116.
[60] Woods, G. F.; Oppelt, J. C.; Isaacson, R. B. J. Am. Chem. Soc. 1960, 82, 5232.
[61] Callot, H. J.; Chevrier, B.; Weiss, R. J. Am. Chem. Soc. 1979, 101, 7730.
[62] Ames, G. R.; Davey, W. J. Chem. Soc. 1957, 3480.
[63] Hoogesteger, F. J.; Havenith, R. W. A.; Zwikker, J. W. J. Org. Chem. 1995, 60, 4375.
[64] Ikeda, H.; Minegishi, T.; Miyash, T. J. Chem. Soc. 1994, 297.
[65] Adam, W.; Grabowski, S.; Miranda, M. A.; Rubenacker, M. J. Chem. Soc. 1988, 142.
[66] Fieser, L. F.; Haddadin, M. J. J. Am. Chem. Soc. 1964, 86, 2392.
[67] Ajaz, A.; McLaughlin, E. C.; Skraba, S. L.; Thamatam, R.; Johnson, R. P. J. Org. Chem. 2012, 77, 9487.

文章导航

/