Synthesis of Bis(iodo-benzopyran) Derivatives and Bis(iodo-2H-quinoline) Derivatives by Electrophilic Cyclization

doi:10.6023/cjoc201402019

Chin. J. Org. Chem. ›› 2014, Vol. 34 ›› Issue (12): 2537-2542.DOI: 10.6023/cjoc201402019 Previous Articles Next Articles

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亲电碘环化反应合成双碘代苯并吡喃衍生物和双碘代1,2-二氢喹啉衍生物

罗倩^a,b, 谢永新^a, 陈朝阳^a, 闫世友^a, 邓文叶^a, 刘义^a,b, 王璐璐^a

a. 中国科学院特殊环境功能材料与器件重点实验室新疆电子信息材料与器件重点实验室中国科学院新疆理化技术研究所乌鲁木齐 830011;
b. 中国科学院大学北京 100049

收稿日期:2014-02-16 修回日期:2014-05-01 发布日期:2014-08-11
通讯作者: 谢永新, 陈朝阳 E-mail:xieyx@ms.xjb.ac.cn;czy@ms.xjb.ac.cn
基金资助:
新疆维吾尔自治区自然科学基金(No.2013211A052)资助项目.

Synthesis of Bis(iodo-benzopyran) Derivatives and Bis(iodo-2H-quinoline) Derivatives by Electrophilic Cyclization

Luo Qian^a,b, Xie Yongxin^a, Chen Zhaoyang^a, Yan Shiyou^a, Deng Wenye^a, Liu Yi^a,b, Wang Lulu^a

a. Key Laboratory of Functional Materials and Devices for Special Environments of Chinese Academy of Sciences, Xinjiang Key Laboratory of Electronic Information Materials and Devices; Xinjiang Technical Institute of Physics & Chemistry, Chinese Academy of Sciences, Urumqi 830011;
b. Graduate University of Chinese Academy of Sciences, Beijing 100049

Received:2014-02-16 Revised:2014-05-01 Published:2014-08-11
Supported by:
Project supported by the Natural Science Foundation of Xinjiang Uygur Autonomous Region of China (No.2013211A052).

Cite this article

Luo Qian, Xie Yongxin, Chen Zhaoyang, Yan Shiyou, Deng Wenye, Liu Yi, Wang Lulu. Synthesis of Bis(iodo-benzopyran) Derivatives and Bis(iodo-2H-quinoline) Derivatives by Electrophilic Cyclization[J]. Chin. J. Org. Chem., 2014, 34(12): 2537-2542.

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[1] (a) Aubert, C.; Buisine, O.; Malacria, M. Chem. Rev. 2002, 102, 813. (b) Wang, X. Y.; Li, Z. Z. Chin. J. Org. Chem. 2014, 34, 566 (in Chinese). (王小勇, 李治章, 有机化学, 2014, 34, 566.) (c) Rubin, M.; Gevorgyan, V. Chem. Rev. 2007, 107, 3117. (d) Nakamura, I.; Yamamoto, Y. Chem. Rev. 2004. 104, 2127. (e) Kitamura, T. Eur. J. Org. Chem. 2009, 1111. (f) Yan, G. B.; Yu, J.; Zhang, L. Chin. J. Org. Chem. 2012, 32, 294 (in Chinese). (严国兵, 于健, 张玲, 有机化学, 2012, 32, 294.)
[2] Mo, J.; Eom, D.; Lee, E.; Lee, P. H. Org. Lett. 2012, 14, 3684.
[3] (a) Zhao, L. B.; Guan, Z. H.; Han, Y.; Xie, Y. X.; He, S.; Liang, Y. M. J. Org. Chem. 2007, 72, 10276. (b) Goto, K.; Yamamoto, G. Tetrahedron Lett. 2001, 42, 4875. (c) Marshall, J. A.; Yanik, M. M. J. Org. Chem. 1999, 64, 3798. (d) Kim, I.; Choi, J.; Won, H. K.; Lee, G. H. Tetrahedron Lett. 2007, 48, 6863. (e) Cherry, K.; Thibonnet, J.; Duchne, A.; Parrain, J. L. Tetrahedron Lett. 2004, 45, 2063. (f) Sakai, N.; Annaka, K.; Fujita, A.; Sato, A.; Konakahara, T. J. Org. Chem. 2008, 73, 4160. (g) Sakai, N.; Annaka, K.; Konakahara, T. Tetrahedron Lett. 2006, 631.
[4] (a) Yue, D.; Larock, R. C. J. Org. Chem. 2002, 67, 1905. (b) Hessian, K.; Flynn, B. Org. Lett. 2003, 5, 4377. (c) Larock, R. C.; Yue, D. Tetrahedron Lett. 2001, 62, 6001.
[5] (a) Arcadi, A.; Cacchi, S.; Giancarlo, F.; Marinelli, F.; Moro, L. Synlett 1999, 1432. (b) Arcadi, A.; Cacchi, S.; Giuseppe, S.; Fabrizi, G.; Marinelli, F. Org. Lett. 2002, 4, 2409. (c). Xie, Y. X.; Liu, X. Y.; Wu, L. Y.; Han, Y.; Zhao, L. B.; Fan, M. J.; Liang, Y. M. Eur. J. Org. Chem. 2008, 1013. (d) Yue, D.; Yao, T.; Larock, R. C. J. Org. Chem. 2005, 70, 10292.
[6] Knight, D. W.; Redfern, A. L.; Gilmore, J. Chem. Commun. 1998, 2207.
[7] (a) Yue, D.; Larock, R. C. Org. Lett. 2004, 6, 1905. (b) Trincado, J.; Rubio, E.; Gonzalez, J. M. Angew. Chem., Int. Ed. 2003, 42, 2406.
[8] (a) Rossi, R.; Carpita, A.; Bellina, F.; Stabile, P.; Mannina, L. Tetrahedron 2003, 59, 2067. (b) Barluenga, J.; Vazquez-Villa, H.; Balles-teros, A.; Gonzalez, J. M. J. Am. Chem. Soc. 2003, 125, 9028. (c) Peng, A. Y.; Ding, Y. X. Org. Lett. 2004, 6, 1119.
[9] Huang, Q.; Hunter, J. A.; Larock, R. C. J. Org. Chem. 2002, 67, 3437.
[10] Mo, J.; Choi, W.; Min, J.; Kim, C. E.; Eom, D.; Kim, S. H.; Lee, P. H. J. Org. Chem. 2013, 78, 11382.
[11] (a) Chen, Y.; Cho, C. H.; Larock, R. C. Org. Lett. 2009, 11, 173. (b) Du, H. A.; Tang, R. Y.; Deng, C. L.; Liu, Y.; Li, J. H. Adv. Synth. Catal. 2011, 353, 2739. (c) Du, H. A.; Zhang, X. G.; Tang, R. Y.; Li, J. H. J. Org. Chem. 2009, 74, 7844. (d) Saito, T.; Horikoshi, T.; Otani, T. Tetrahedron Lett. 2003, 44, 6513. (e) Yadav, J. S.; Reddy, B. V. S.; Rao, C. V. J. Chem. Soc. 2002, 11, 1401. (f) Luo, S. P.; Tang, R. Y.; Zhong, P.; Li, J. H. Chin. J. Org. Chem. 2009, 29, 1924 (in Chinese). (罗培松, 汤日元, 钟平, 李金恒, 有机化学, 2009, 29, 1924.) (g) Diaba, F.; Ricou, E. Bonjoch, J. Org. Lett. 2007, 9, 2633. (h) Ma, S. M.; Lu, L. H. J. Org. Chem. 2005, 70, 7629. (i) Liu, Y. H.; Zhou, S. L. Org. Lett, 2005, 7, 4609.

亲电碘环化反应合成双碘代苯并吡喃衍生物和双碘代1,2-二氢喹啉衍生物

Synthesis of Bis(iodo-benzopyran) Derivatives and Bis(iodo-2H-quinoline) Derivatives by Electrophilic Cyclization

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