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...
化学进展  2012 

氮杂吲哚合成

, PP. 1974-1982

Keywords: 氮杂吲哚,有机合成,过渡金属

Full-Text   Cite this paper   Add to My Lib

Abstract:

氮杂吲哚是一类重要的杂环分子,在材料科学以及药物设计与合成中具有重要地位。由于氮杂吲哚在结构上区别于吲哚,所以一些经典的合成吲哚的方法并不很适用于氮杂吲哚的合成。近年来,金属有机化学的发展为氮杂吲哚的合成提供了更多的原料选择以及更有效的成环方式,从而为氮杂吲哚的合成开辟了新的方向。本文综述了氮杂吲哚有机合成方法学近年来的进展,介绍了通过Bartoli合成、Fischer吲哚合成、有机锂试剂、过渡金属促进以及其他方法来合成氮杂吲哚类化合物的研究,总结了合成各类氮杂吲哚(4-氮杂吲哚、5-氮杂吲哚、6-氮杂吲哚以及7-氮杂吲哚)的常用有机合成方法,为促进氮杂吲哚类化合物在药物合成化学以及材料科学方面的应用提供了基础。

References

[1]  Zhao S B, Wang S. Chem. Soc. Rev., 2010, 39: 3142-3156
[2]  Song J J, Reeves J T, Gallou F, Tan Z, Yee N K, Senanayake C H. Chem. Soc. Rev., 2007, 36: 1120-1132
[3]  Blaazer A R, Lange J H M, van der Neut M A W, Mulder A, den Boon F S, Werkman T R, Kruse C G, Wadman W J. Eur. J. Med. Chem., 2011, 46: 5086-5098
[4]  Lachance N, Bonhomme-Beaulieu L P, Joly P. Synthesis, 2009, 721-730
[5]  Jeanty M, Blu J, Suzenet F, Guillaumet G. Org. Lett., 2009, 11: 5142-5145
[6]  Luo Q, Gu L, Wang C, Liu J, Zhang W, Xi Z. Tetrahedron Lett., 2009, 50: 3213-3215
[7]  Liu J, Zhang S, Zhang W X, Xi Z. Organometallic, 2009, 28: 413-417
[8]  Yu T, Sun X, Wang C, Deng L, Xi Z. Chem. Eur. J., 2005, 11: 1895-1902
[9]  Zhang W X, Zhang S, Sun X, Nishiura M, Hou Z, Xi Z. Angew. Chem. Int. Ed., 2009, 48: 7227-7231
[10]  Zhang S, Zhang W X, Zhao J, Xi Z. J. Am. Chem. Soc., 2010, 132: 14042-14045
[11]  Zhang S, Sun X, Zhang W X, Xi Z. Chem. Eur. J., 2009, 15: 12608-12617
[12]  Zhang S, Zhang W X, Zhao J, Xi Z. Chem. Eur. J., 2011, 17: 2442-2449
[13]  Zhang S, Zhang W X, Xi Z. Chem. Eur. J., 2010, 16: 8419-8426
[14]  Zhang S, Zhao J, Zhang W X, Xi Z. Org. Lett., 2011, 13: 1626-1629
[15]  Layek M, Kumar Y S, Islam A, Karavarapu R, Sengupta A, Halder D, Mukkanti K, Pal M. Med. Chem. Commun., 2011, 2: 478-485
[16]  Tjosaas F, Kjerstad I B, Fiksdahl A. J. Heterocyclic Chem., 2008, 45: 559-562
[17]  Gorugantula S P, Carrero-Mart韓ez G M, Dantale S W, S?derberg B C G. Tetrahedron, 2010, 66: 1800-1805
[18]  Hodgkinson R C, Schulz J, Willis M C. Org. Biomol. Chem., 2009, 7: 432-434
[19]  Jia Y, Zhu J. Synlett, 2005, 2469-2472
[20]  Jia Y, Bois-Choussy M, Zhu J. Angew. Chem. Int. Ed., 2008, 47: 4167-4172
[21]  Xu Z, Hu W, Zhang F, Li Q, L? Z, Zhang L, Jia Y. Synthesis, 2008, 3981-3987
[22]  Spergel S H, Okoro D R, Pitts W. J. Org. Chem., 2010, 75: 5316-5319
[23]  Whelligan D K, Thomson D W, Taylor D, Hoelder S. J. Org. Chem., 2010, 75: 11-15
[24]  Shumaila A M A, Puranik V G, Kusurkar R S. Tetrahedron, 2011, 67: 936-942
[25]  Lu J, Cai X, Hecht S M. Org. Lett., 2010, 12: 5189-5191
[26]  Joule J A, Mills K. Heterocyclic Chemistry (5th ed.). Blackwell: Wiley, 2010. 373-431
[27]  Popowycz F, Mérour J Y, Joseph B. Tetrahedron, 2007, 63: 8689-8707
[28]  Popowycz F, Routier S, Joseph B, Mérour J Y. Tetrahedron, 2007, 63: 1031-1064
[29]  Ma Y, Breslin S, Keresztes I, Lobkovsky E, Collum D B. J. Org. Chem., 2008, 73: 9610-9618
[30]  Kurhade S, Kaduskar R D, Dave B, Ramaiah P A, Palle V P, Bhuniya D. Tetrahedron Lett., 2011, 52: 1874-1877
[31]  Zhang W X, Zhang S, Xi Z. Acc. Chem. Res., 2011, 44: 541-551
[32]  Luo Q, Wang C, Gu L, Zhang W X, Xi Z. Chem. Asian J., 2010, 5: 1120-1128
[33]  Yu T, Deng L, Zhao C, Li Z, Xi Z. Tetrahedron Lett., 2003, 44: 677-679
[34]  Xi Z, Fischer R, Hara R, Sun W, Obora Y, Suzuki N, Nakajima K, Takahashi T. J. Am. Chem. Soc., 1997, 119: 12842-12848
[35]  Takahashi T, Xi Z, Obora Y, Suzuki N. J. Am. Chem. Soc., 1995, 117: 2665-2666
[36]  Sun X, Wang C, Li Z, Zhang S, Xi Z. J. Am. Chem. Soc., 2004, 126: 7172-7173
[37]  Calvet G, Livecchi M, Schmidt F. J. Org. Chem., 2011, 76: 4734-4740
[38]  Koolman H, Heinrich T, B?ttcher H, Rautenberg W, Reggelin M. Bioorg. Med. Chem. Lett., 2009, 19: 1879-1882
[39]  Suzuki Y, Ohta Y, Oishi S, Fujii N, Ohno H. J. Org. Chem., 2009, 74: 4246-4251
[40]  Majumdar K C, Mondal S. Tetrahedron Lett., 2007, 48: 6951-6953
[41]  Majumdar K C, Samanta S, Chattopadhyay B. Tetrahedron Lett., 2008, 49: 7213-7216
[42]  Liang Y, Zhang S, Xi Z. J. Am. Chem. Soc., 2011, 133: 9204-9207
[43]  Liang Y, Meng T, Zhang H J, Xi Z. Synlett, 2011, 911-914
[44]  Hodgkinson R C, Schulz J, Willis M C. Tetrahedron, 2009, 65: 8940-8949
[45]  Fang Y Q, Yuen J, Lautens M. J. Org. Chem., 2007, 72: 5152-5160
[46]  Wang Z, Bois-Choussy M, Jia Y, Zhu J. Angew. Chem. Int. Ed., 2010, 49: 2018-2022
[47]  Velthuisen E J, Danishefsky S J. J. Am. Chem. Soc., 2007, 129: 10640-10641
[48]  Moustafa M M A R, Pagenkopf B L. Org. Lett., 2010, 12: 3168-3171
[49]  Parcerisa J, Romero M, Pujol M D. Tetrahedron, 2008, 64: 500-507
[50]  Carpita A, Ribecai A, Stabile P. Tetrahedron, 2010, 66: 7169-7178
[51]  Jeanty M, Suzenet F, Guillaumet G. J. Org. Chem., 2008, 73: 7390-7393

Full-Text

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133