全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...
催化学报  2015 

通过η3-苄基钯中间体零价钯催化的吲哚苄基化反应

DOI: 10.1016/S1872-2067(14)60191-1, PP. 15-18

Keywords: 苄基化,吲哚,三芳基甲烷,η3-苄基钯中间体

Full-Text   Cite this paper   Add to My Lib

Abstract:

?本文报道了零价钯催化的吲哚苄基化反应,获得了优秀的区域选择性.使用Pd(PPh3)4作为催化剂,在温和反应条件下,以90%-99%的收率获得含有各类取代吲哚片段的三芳基甲烷化合物.

References

[1]  Kuwano R. Synthesis, 2009: 1049
[2]  Zhu Y, Rawal V H. J Am Chem Soc, 2012, 134: 111
[3]  Lakhdar S, Westermaier M, Terrier F, Goumont R, Boubaker T, Ofial A R, Mayr H. J Org Chem, 2006, 71: 9088
[4]  Skurydina D F, Tolkachev V N, Zenkina D I, Nikolaeva T G, Tolkachev O N. Pharm Chem J, 2008, 42: 443
[5]  Duxbury D F. Chem Rev, 1993, 93: 381
[6]  Shchepinov M S, Korshun V A. Chem Soc Rev, 2003, 32: 170
[7]  Nair V, Thomas S, Mathew S C, Abhilash K G. Tetrahedron, 2006, 62: 6731
[8]  He Q L, Sun F L, Zheng X J, You S L. Synlett, 2009: 1111
[9]  Sun F L, Zheng X J, Gu Q, He Q L, You S L. Eur J Org Chem, 2010: 47
[10]  Wu K, Jiang Y J, Fan Y S, Sha D, Zhang S Q. Chem Eur J, 2013, 19: 474
[11]  Pape A R, Kaliappan K P, Kündig E P. Chem Rev, 2000, 100: 2917
[12]  Roche S P, Porco J A Jr. Angew Chem Int Ed, 2011, 50: 4068
[13]  Zhuo C X, Zhang W, You S L. Angew Chem Int Ed, 2012, 51: 12662
[14]  Zhuo C X, Zheng C, You S L. Acc Chem Res, 2014, 47: 2558
[15]  Tsuji J. Palladium Reagents and Catalysts. Chichester: John Wiley & Sons, 2004. 431
[16]  Zhang X, Feng X J, Liu H S, Qin Y H, Dai Y. Chin J Catal (张新, 冯秀娟, 刘鹤松, 秦余虎, 戴耀. 催化学报), 2012, 33: 523
[17]  Kuwano R, Kondo Y, Matsuyama Y. J Am Chem Soc, 2003, 125: 12104
[18]  Kuwano R, Kondo Y. Org Lett, 2004, 6: 3545
[19]  Ueno S, Komiya S, Tanaka T, Kuwano R. Org Lett, 2012, 14: 338
[20]  Trost B M, Czabaniuk L C. J Am Chem Soc, 2010, 132: 15534
[21]  Mukai T, Hirano K, Satoh T, Miura M. Org Lett, 2010, 12: 1360
[22]  Legros J Y, Toffano M, Fiaud J C. Tetrahedron: Asymmetry, 1995, 6: 1899
[23]  Trost B M, Czabaniuk L C. J Am Chem Soc, 2012, 134: 5778
[24]  Trost B M, Czabaniuk L C. Chem Eur J, 2013, 19: 15210
[25]  Legros J Y, Primault G, Toffano M, Rivière M A, Fiaud J C. Org Lett, 2000, 2: 433
[26]  Yokogi M, Kuwano R. Tetrahedron Lett, 2007, 48: 6109
[27]  Assié M, Meddour A, Fiaud J C, Legros J Y. Tetrahedron: Asymmetry, 2010, 21: 1701
[28]  Fields W H, Chruma J J. Org Lett, 2010, 12: 316
[29]  Torregrosa R R P, Ariyarathna Y, Chattopadhyay K, Tunge J A. J Am Chem Soc, 2010, 132: 9280
[30]  Blessley G, Holden P, Walker M, Brown J M, Gouverneur V. Org Lett, 2012, 14: 2754
[31]  Bao M, Nakamura H, Yamamoto Y. J Am Chem Soc, 2001, 123: 759
[32]  Ariafard A, Lin Z Y. J Am Chem Soc, 2006, 128: 13010
[33]  Lu S R, Xu Z W, Bao M, Yamamoto Y. Angew Chem Int Ed, 2008, 47: 4366
[34]  Peng B, Feng X J, Zhang X, Ji L Y, Bao M. Tetrahedron, 2010, 66: 6013
[35]  Peng B, Feng X J, Zhang X, Zhang S, Bao M. J Org Chem, 2010, 75: 2619
[36]  Peng B, Zhang S, Yu X Q, Feng X J, Bao M. Org Lett, 2011, 13: 5402
[37]  Feng X J, Sun A L, Zhang S, Yu X Q, Bao M. Org Lett, 2013, 15: 108
[38]  Zhang X, Feng X J, Yu X Q, He R, Bao M. Org Biomol Chem, 2013, 11: 4016
[39]  Feng X J, Song J L, Liu H S, Wang L G, Yu X Q, Bao M. RSC Adv, 2013, 3: 18985
[40]  Zhang S, Wang Y, Feng X J, Bao M. J Am Chem Soc, 2012, 134: 5492
[41]  Zhang S, Bao M. Synlett, 2012, 23: 2431
[42]  Kuwano R, Kusano H. Org Lett, 2008, 10: 1979
[43]  Kuwano R, KondoY, Shirahama T. Org Lett, 2005, 7: 2973
[44]  Johns A M, Tye J W, Hartwig J F. J Am Chem Soc, 2006, 128: 16010

Full-Text

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133