English
新闻公告
More
化学进展 2013, Vol. 25 Issue (07): 1142-1148 DOI: 10.7536/PC121127 前一篇   后一篇

• 综述与评论 •

芳基碘鎓盐促进芳基化反应的应用

张变香*, 赵晓芸, 吴群, 郭一力   

  1. 山西大学化学化工学院 太原 030006
  • 收稿日期:2012-11-01 修回日期:2013-03-01 出版日期:2013-07-25 发布日期:2013-04-16
  • 通讯作者: 张变香 E-mail:zbxthh@sxu.edu.cn
  • 基金资助:

    山西省科技攻关项目(No.0110321040-02)、山西省回国留学人员科研项目(No.2010-001)、山西省科技基础条件平台项目(No.2013091026)和山西大学本科生科研训练项目(No. 2012010055)资助

Application of Diaryliodonium Salts in Arylation Reaction

Zhang Bianxiang*, Zhao Xiaoyun, Wu Qun, Guo Yili   

  1. School of Chemistry and Chemical Engineering, Shanxi University, Taiyuan 030006, China
  • Received:2012-11-01 Revised:2013-03-01 Online:2013-07-25 Published:2013-04-16

二芳基碘鎓盐属于有机高价碘化合物,具有无毒、反应条件温和以及良好的选择性等优点,在有机合成中具有重要地位,受到广大化学工作者的关注。近年来,利用二芳基碘鎓盐在金属催化下进行的芳基化反应为一些难以合成的杂环化合物的合成提供了简便、高效的方法;同时,二芳基碘鎓盐在无催化剂下进行的芳基化反应,为C-C偶联反应开辟了新的绿色合成路线。本文综述了近年来二芳基碘鎓盐在有机合成中促进芳基化反应的最新进展,着重介绍了利用二芳基碘鎓盐作为芳基化试剂与有机金属试剂、烯烃和炔烃类以及杂环化合物进行芳基化反应的研究;总结了二芳基碘鎓盐与杂环化合物反应中钯催化和铜催化下芳基化反应的机理,最后对二芳基碘鎓盐在今后有机合成中的应用作出了展望。

Diaryliodonium salt is one of the hypervalent organoiodine species, which has many advantages including non-toxic, mild conditions and excellent selectivity in reactions. It is highly important in organic synthesis and attracts many chemists’ attention. Recently, the arylation reaction by diaryliodonium salts under metal catalysts provides a simple and efficient way to synthesize heterocyclic compounds which are difficult to synthesize, in addition, the emergence of arylation reaction under no metal catalytic conditions has made a green synthesis route for C-C coupling reactions. We review the arylation reactions by diaryliodonium salts in recent years, especially the reactions between diaryliodonium salts with organometallic reagents, alkenes, alkynes and heterocyclic compounds, and summarize the mechanisms of arylation reactions between diaryliodonium salts and heterocyclic compounds with palladium, copper catalysts or without metal catalysts. The development trend of applications in organic synthesis of diaryliodonium salts is also prospected. Contents
1 Introduction
2 Arylation of organometallic reagents
3 Arylation of alkenes or alkynes
4 Arylation of heterocyclic compounds
5 Other types of arylation reaction
6 Conclusion and outlook

中图分类号: 

()

[1] Willgerodt C. J. Prakt. Chem., 1886, 33: 154-160
[2] Hartmann C, Meyer V. Chem. Ber., 1894, 27: 426-432
[3] Stang P J. Chem. Rev. 1996, 96: 1123-1178
[4] Zhdankin V V, Stang P J. Chem. Rev., 2002, 102: 2523-2584
[5] Zhdankin V V, Stang P J. Chem. Rev., 2008, 108: 5299-5358
[6] 李润明(Li R M), 屈菊平(Qu J P), 高青雨(Gao Q Y). 化学研究(Chemical Research), 1999, 10(4): 48-53
[7] 张变香(Zhang B X), 魏保利(Wei B L). 中国涂料(China Coatings), 2011, 26(4): 31-35
[8] 谢川(Xie C), 李海燕(Li H Y). 四川大学学报(工程科学版)(Jouranal of Sichuan University ( Engineering Science Edition)), 2006, 38(6): 68-72
[9] 翟媛萍(Zhai Y P), 杨辉(Yang H). 化学学报(Acta Chimica Sinica), 2007, 65(13): 1253-1257
[10] 邹菁(Zou J), 刘安昌(Liu A C), 李蕾(Li L), 乐婷(Yue T), 陆永章(Lu Y Z). 化学与生物工程(Chemistry & Bioengineering), 2006, 23(6): 58-60
[11] 赵迎娣(Zhao Y D). 有机化学(Chinese Journal of Organic Chemistry), 1996, 1: 11-17
[12] 潘振良(Pan Z L), 沈永雯(Shen Y W), 梁永民(Liang Y M). 化学进展(Progress in Chemistry), 2007, 19(2/3): 303-312
[13] Zefirov N S, Kasumov T M, Koz’min A S, Sorokin V D, Stang P J, Zhdankin V V. Synthesis, 1993, 12: 1209-1210
[14] 梁永民(Liang Y M), 陈保华(Chen B H), 武小莉(Wu X L), 马永祥(Ma Y X). 合成化学(Chinese Journal of Synthetic Chemistry), 2002, 10(2): 98-105
[15] Kitamura T, Matsuyuki J, Tanigchi H. Synthesis, 1994, 2: 147-148
[16] Deprez N R, Sanford M S. Inorg. Chem., 2007, 46: 1924-1935
[17] Deprez N R, Sanford M S. J. Am. Chem. Soc., 2009, 131: 11234-11241
[18] 夏敏(Xia M), 陈振初(Chen Z C). 株洲工学院学报(Journal of Zhuzhou Institute of Technology), 1999, 13(5): 56-62
[19] 石启英(Shi Q Y). 有机化学(Chinese Journal of Organic Chemistry), 2004, 24(8): 912-915
[20] Xiao B, Fu Y, Xu J, Gong T J, Dai J J, Yi J, Liu L. J. Am. Chem. Soc., 2010, 132: 468-469
[21] 吴杰(Wu J), 谢益明(Xie Y M). 甘肃科技(Gansu Science and Technology), 2011, 27(11): 24-26
[22] Castro S, Fernandez J J, Vicente R, Fananas F J, Rodrigiez F. Chem. Commun., 2012, 48: 9089-9091
[23] Zhang S L, Ding Y Q. Chin. J. Chem. Phys., 2011, 24: 711-723
[24] Kuriyama M, Hamaguchi N, Onomura O. Chem. Eur. J., 2012, 18: 1591-1594
[25] Kang S K, Yamaguchi T, Ho P S, Kim W Y, Yoon S K. Tetrahedron Lett., 1997, 38: 1947-1950
[26] Kang S K, Lee Y T, Lee S H. Tetrahedron Lett., 1999, 40: 3573-3576
[27] Kang S K, Kim W Y, Lee Y T, Ahn S K, Kim J C. Tetrahedron Lett., 1998, 39: 2131-2132
[28] Kang S K, Lee H W, Jang S B, Ho P S. J. Org. Chem., 1996, 61: 4720-4724
[29] Hatanaka Y, Hiyama T. J. Am. Chem. Soc., 1990, 112: 7793-7794
[30] Kang S K, Yamaguchi T, Hong R K, Kim T H, Pyun S J. Tetrahedron, 1997, 53: 3027-3034
[31] Kang S K, Tokutaro Yamaguchi, Kim T H, Ho P S. J. Org. Chem., 1996, 61: 9082-9083
[32] Wirth T, Hirt U H. Synthesis, 1999, 8: 1271-1287
[33] Heck R F. Organic Reactions, 1982, 27: 345-390
[34] Werner E W, Sigman M S. J. Am. Chem. Soc., 2011, 133: 9692-9695
[35] Daves G D, Hallberg A. Chem. Rev., 1989, 89: 1433-1445
[36] Kang S K, Lee H W, Jang S B, Kim T H, Pyun S J. J. Org. Chem., 1996, 61: 2604-2605
[37] Tamaru Y, Yamada Y, Yoshida Z. J. Org. Chem., 1978, 43: 3396-3398
[38] Radhakrishnan U, Stang P J. Org. Lett., 2001, 3: 859-860
[39] Sakamoto T, Shiga F, Yasuhara A, Uchiyama D, Kondo Y, Yamanaka H. Synthesis, 1992, 8: 746-748
[40] Kundu N G, Dasgupta S K. J. Chem. Soc. Perkin Trans. 1, 1993, 2657-2663
[41] Kang S K, Yoon S K, Kim Y M. Org. Lett., 2001, 3: 2697-2699
[42] Sonogashira K, Tohda Y, Hagihara N. Tetrahedron Lett., 1975, 16: 4467-4470
[43] Hundertmark T, Littke A F, Buchwald S L, Fu G C. Org. Lett., 2000, 2: 1729-1730
[44] 柯 城(Ke C), 唐星华(Tang X H), 吴雪梅(Wu X M), 郑 重(Zheng Z). 江西科学(Jiangxi Science), 2008, 26(3): 426-429
[45] Phipps R J, Murray L M, Ritter S, Duong H A, Gaunt M J. J. Am. Chem. Soc., 2012, 134: 10773-10776
[46] Vallée F, Mousseau J J, Charette A B. J. Am. Chem. Soc., 2010, 132: 1514-1516
[47] Bellina B, Rossi R. Tetrahedron, 2009, 65: 10269-10310
[48] Zaitsev V G, Shabashov D, Daugulis O. J. Am. Chem. Soc., 2005, 127: 13154-13155
[49] Lane B S, Brown M A, Sames D. J. Am. Chem. Soc., 2005, 127: 8050-8057
[50] Lane B S, Sames D. Org. Lett., 2004, 6: 2897-2900
[51] Sezen B, Sames D. J. Am. Chem. Soc, 2003, 125: 5274-5275
[52] Deprez N R, Kalyani D, Krause A, Sanford M S. J. Am. Chem. Soc., 2006, 128: 4972-4973
[53] Kalyani D, Deprez N R, Desai L V, Sanford M S. J. Am. Chem. Soc., 2005, 127: 7330-7331
[54] Lyons T W, Sanford M S. Chem. Rev., 2010, 110: 1147-1169
[55] Wagner A M, Sanford M S. Org. Lett., 2011, 13: 288-291
[56] Yang Q, Chang J, Wu Q, Zhang B X. Res. Chem. Intermed., 2012, 38: 1335-1340
[57] Phipps R J, Grimster N P, Gaunt M J. J. Am. Chem. Soc., 2008, 130: 8172-8174
[58] Lebrasseur N, Larrosa I. J. Am. Chem. Soc., 2008, 130: 2926-2927
[59] Dwight T A, Rue N R, Charyk D, Josselyn R, Boef B D. Org. Lett., 2007, 9: 3137-3139
[60] Jafarpour F, Rahiminejadan S, Hazrat H. J. Org. Chem., 2010, 75: 3109-3112
[61] Wang X, Gribkov D V, Sames D. J. Org. Chem., 72: 1476-1479
[62] Kitamura T, Yamane M, Zhang B X, Fujiwra Y. Bull. Chem. Soc. Jpn., 1998, 71: 1215-1219
[63] 张变香(Zhang B X), 常姣(Chang J), 杨祺(Yang Q), 吴群(Wu Q). 有机化学(Chinese Journal of Organic Chemistry), 2012, 32: 1150-1156
[64] Beringer F M, Gindler E M, Rapoport M, Tayler R J. J. Am. Chem. Soc., 1959, 81: 351-361
[65] Caserio M C, Glusker D L, Roberts J D. J. Am. Chem. Soc., 1959, 81: 336-342
[66] Lockhart T P. J. Am. Chem. Soc., 1983, 105: 1940-1946
[67] Zhang B X, Nuka T, Fujiwara Y, Yamaji T, Hou Z, Kitamura T. Heterocycles, 2004, 64: 199-206
[68] Wen J, Zhang R Y, Chen S Y, Zhang J, Yu X Q. J. Org. Chem., 2012, 77: 766-771
[69] Ackermann L, Acqua M D, Fenner S, Vicente R, Sandmann R. Org. Lett., 2011, 23: 2358-2360
[70] Carroll M A, Wood R A. Tetrahedron, 2007, 63: 11349-11354
[71] Jalalian N, Ishikawa E E, Silva L F Jr, Olofsson B. Org. Lett., 2011, 13: 1552-1555
[72] 杨祺(Yang Q), 和潇夏(He X X), 常姣(Chang J), 吴群(Wu Q), 张变香(Zhang B X). 有机化学(Chinese Journal of Organic Chemistry), 2011, 31: 1687-1689
[73] Chen D W, Takai K, Ochiai M. Tetrahedron Lett., 1997, 38: 8211-8214

[1] 白文己, 石宇冰, 母伟花, 李江平, 于嘉玮. Cs2CO3辅助钯催化X—H (X=C、O、N、B)官能团化反应的理论计算研究[J]. 化学进展, 2022, 34(10): 2283-2301.
[2] 商天奕, 吕琪妍, 刘琰, 於兵. Ugi/Diels-Alder串联反应在构建杂环化合物中的应用[J]. 化学进展, 2019, 31(10): 1362-1371.
[3] 窦言东, 顾晓旭, 蒋建泽, 朱勍. 导向基团辅助的C—H键功能化[J]. 化学进展, 2018, 30(9): 1317-1329.
[4] 戴立信*. Ullmann反应百年纪念及近期复兴——兼及碳-杂原子键的形成[J]. 化学进展, 2018, 30(9): 1257-1297.
[5] 韩志勇, 龚流柱*. 手性有机小分子和钯联合不对称催化[J]. 化学进展, 2018, 30(5): 505-512.
[6] 陈劲进, 常丹, 肖福红, 邓国军*. 基于环己酮氧化脱氢构建碳-碳与碳-杂键[J]. 化学进展, 2018, 30(5): 564-577.
[7] 孔令斌, 严胜骄*, 林军*. 杂环烯酮缩胺:构筑分子多样性稠杂环化合物的合成先导分子[J]. 化学进展, 2018, 30(5): 639-657.
[8] 张晓鹏*, 董淑祥, 范学森, 张贵生. 邻氨基苯甲酰胺类化合物的合成[J]. 化学进展, 2017, 29(11): 1351-1356.
[9] 范观铭, 韩骞, 熊兴泉. 基于无铜点击反应的水凝胶合成[J]. 化学进展, 2014, 26(07): 1223-1232.
[10] 金小平, 张莉, 高浩其, 房江华, 李瑞丰, 方烨汶. 钯和铜催化的脂肪醇和芳基卤代烃偶联反应[J]. 化学进展, 2013, 25(11): 1898-1905.
[11] 盘登芳, 叶钢, 王芳, 陈靖* . 含氮杂环化合物萃取分离三价锕系与镧系元素[J]. 化学进展, 2012, 24(11): 2167-2176.
[12] 江玉波, 匡春香. 1, 2, 3-三氮唑衍生物的合成[J]. 化学进展, 2012, (10): 1983-1994.
[13] 沈金海, 程国林, 崔秀灵*. 基于钯催化C-H键活化的多米诺反应[J]. 化学进展, 2012, 24(07): 1324-1336.
[14] 翁建全, 余志勤, 张国富. 非官能化芳烃与烯烃的直接氧化偶联反应[J]. 化学进展, 2012, 24(04): 523-544.
[15] 王丽丽 赵伟宁 段征. K4[Fe(CN)6]作为氰源在氰基化反应中的应用**[J]. 化学进展, 2010, 22(10): 1964-1972.