中文
Announcement
More
Progress in Chemistry 2005, Vol. 17 Issue (06): 1041-1047 Previous Articles   Next Articles

• Review •

Progress of Synthesis and Applications of Organoaluminacycles

Fang Hongyun;Xi Zhenfeng**   

  1. College of Chemistry &Molecular Engineering,Peking University,Beijing 100871,China
  • Received: Revised: Online: Published:
  • Contact: Xi Zhenfeng
PDF ( 2528 ) Cited
Export

EndNote

Ris

BibTeX

Recent progress of synthesis and applications of organoaluminacycles is summarized. As synthetic methods for organoaluminacycles,carboalumination or hydroalumination of alkynes followed by thermal elimination,reaction of di2organolithium reagents with aluminum halides,and zirconocene2catalyzed reactions of alkynes with AlR3 have been developed.Useful synthetic reactions of organoaluminacycles ,such as reactions with a variety of electrophiles,alkylation reagents,and metal2mediated coupling reactions are presented.

CLC Number: 

[ 1 ] 王积涛(Wang J T) , 宋礼成( Song L C) 1 金属有机化学( Organometallic Chemistry ) . 高等教育出版社( Higher Education Press) , 1989. 77 —77
[ 2 ] 王积涛(Wang J T) , 宋礼成(Song L C) . 金属有机化学( Organometallic Chemistry ) . 高等教育出版社( Higher Education Press) , 1989. 82 —82
[ 3 ] 麻生明(Ma S M) . 金属参与的现代有机合成反应(Metal Mediated Organic Synthesis) , 第二版(2nd ed) . 广东科技出版社(Guangdong Science and Technology Press) , 2003. 192 —192
[ 4 ] Eisch J J , Kaska W C. J . Am. Chem. Soc. , 1962 , 84 : 1501 —1502
[ 5 ] Eisch J J , Kaska W C. J . Am. Chem. Soc. , 1966 , 88 : 2976 —2983
[ 6 ] Eisch J J , Healy M E. J . Am. Chem. Soc. , 1964 , 86 : 4221 —4222
[ 7 ] Eisch J J , Hordis C K. J . Am. Chem. Soc. , 1971 , 93 : 2974 —2981
[ 8 ] Hata G, Miyake A. J . Org. Chem. , 1963 , 28 : 3237 —3238
[ 9 ] Hoberg H , Krause-Going R. J . Organomet . Chem. , 1977 , 127 :C29 —C31
[10] Kruger C , Sekutowski J C , Hoberg H , Krause-Going R. J .Organomet . Chem. , 1977 , 141 : 141 —148
[11] Hoberg H , Gotor V , Milchereit A , Kruger C , Sekutowski J C.Angew. Chem. Int . Ed. Engl . , 1977 , 16 : 539 —540
[12] Hoberg H , Krause-Going R , Kruger C , Sekutowski J C. Angew.Chem. Int . Ed. Engl . , 1977 , 16 : 183 —184
[13] Van Horn D E , Negishi E. J . Am. Chem. Soc. , 1978 , 100 :2252 —2254
[14] Negishi E , Yoshida T. Tetrahedron Lett . , 1980 , 21 : 1501 —1504
[15] Negishi E , van Horn D E , Yoshida T. J . Am. Chem. Soc. ,1985 , 107 : 6639 —6647
[16] Negishi E , Takahashi T. Synthesis , 1988 , 1 : 1 —19
[17] Rand C L , van Horn D E , Moore M W, Negishi E. J . Org.Chem. , 1981 , 46 : 4093 —4096
[18] Negishi E , van Horn D E , Yoshida T. J . Am. Chem. Soc. ,1985 , 107 : 6639 —6647
[19] Dzhemilev U M, Ibragimov A G. J . Organomet . Chem. , 1994 ,466 : 1 —4
[20] Dzhemilev U M. Tetrahedron Lett . , 1995 , 15 : 4333 —4346
[21] Dawson G, Durrant C A , Kirk G G, Whitby R J . Tetrahedron Lett . , 1997 , 13 : 2335 —2338
[22] Negishi E , Kondakov D Y, Choueiry D , Kasai K, Takahashi T.J . Am. Chem. Soc. , 1996 , 118 : 9577 —9588
[23] Dzhemilev U M, Vostrikova O S. J . Organomet . Chem. , 1985 ,285 : 43 —51
[24] Chenier J H , Howard J A , Mile B. J . Am. Chem. Soc. , 1987 ,109 : 4109 —4110
[25] Joly H A , Kepes M, Roy N , Prpic J . Can. J . Chem. , 1998 ,76 : 400 —406
[26] Chenier J H , Howard J A , Tse J S , Mile B. J . Am. Chem.Soc. , 1985 , 107 : 7290 —7294
[27] Negishi E , Montchamp J , Anastasia L , Elizarov A , Choueiry D.Tetrahedron Lett . , 1998 , 39 : 2503 —2506
[28] Dubac J , Laporterie A , Manuel G. Chem. Rev. , 1990 , 90 :215 —263
[29] Ashe A J Ⅲ, Kampf J W, Al-Taweel S M. J . Am. Chem. Soc. ,1992 , 114 : 372 —374
[30] Ashe A J Ⅲ, Al-Ahmad S , Pilotek S , Puranik D B , Elschenbroich C , Behrendt A. Organometallics , 1995 , 14 : 2689 —2698
[31] Bankwitz U , Sohn H , Powell D R , West R J . Organomet .Chem. , 1995 , 499 : C7 —C9
[32] Freeman W P , Tilley T D , Liable-Sands L M, Rheingold A L. J .Am. Chem. Soc. , 1996 , 118 : 10457 —10468
[33] Yamaguchi S , Jin R , Tamao K. J . Organomet . Chem. , 1998 ,559 : 73 —80
[34] Xi C , Huo S , Afifi T , Hara R , Takahashi T. Tetrahedron Lett . ,1997 , 38 : 4099 —4102
[35] Fang H Y, Zhao C J , Li G T , Xi Z F. Tetrahedron , 2003 , 59 :3779 —3786
[36] Dzhemilev U M, Ibragimov A G, Khafizova L O , Ramazanov I R ,Yalalova D F , Toslstikov G A. J . Organomet . Chem. , 2001 ,636 : 76 —81
[37] Eisch J J , Husk G R. J . Org. Chem. , 1966 , 31 : 3419 —3422
[38] Ma S , Negishi E. J . Org. Chem. , 1997 , 62 : 784 —785
[39] 麻生明(Ma S M) . 金属参与的现代有机合成反应(Metal Mediated Organic Synthesis) , 第二版(2nd ed) . 广东科技出版社(Guangdong Science and Technology Press) , 2003. 193 —194
[40] Kondakov D Y, Negishi E. J . Am. Chem. Soc. , 1995 , 117 :10771 —10772
[41] Knodakov D Y, Negishi E. J . Am. Chem. Soc. , 1996 , 118 :1577 —1578

[1] Jing He, Jia Chen, Hongdeng Qiu. Synthesis of Traditional Chinese Medicines-Derived Carbon Dots for Bioimaging and Therapeutics [J]. Progress in Chemistry, 2023, 35(5): 655-682.
[2] Jianfeng Yan, Jindong Xu, Ruiying Zhang, Pin Zhou, Yaofeng Yuan, Yuanming Li. Nanocarbon Molecules — the Fascination of Synthetic Chemistry [J]. Progress in Chemistry, 2023, 35(5): 699-708.
[3] Xinyue Wang, Kang Jin. Chemical Synthesis of Peptides and Proteins [J]. Progress in Chemistry, 2023, 35(4): 526-542.
[4] Liu Yvfei, Zhang Mi, Lu Meng, Lan Yaqian. Covalent Organic Frameworks for Photocatalytic CO2 Reduction [J]. Progress in Chemistry, 2023, 35(3): 349-359.
[5] Zixuan Liao, Yuhui Wang, Jianping Zheng. Research Advance of Carbon-Dots Based Hydrophilic Room Temperature Phosphorescent Composites [J]. Progress in Chemistry, 2023, 35(2): 263-373.
[6] Yehjun Lim, Yanmei Li. Chemical Synthesis/Semisynthesis of Post-Translational Modified Tau Protein [J]. Progress in Chemistry, 2022, 34(8): 1645-1660.
[7] Peng Xu, Biao Yu. Challenges in Chemical Synthesis of Glycans and the Possible Problems Relevant to Condensed Matter Chemistry [J]. Progress in Chemistry, 2022, 34(7): 1548-1553.
[8] Deshan Zhang, Chenho Tung, Lizhu Wu. Artificial Photosynthesis [J]. Progress in Chemistry, 2022, 34(7): 1590-1599.
[9] Shuaiwei Peng, Zhuofu Tang, Bing Lei, Zhiyuan Feng, Honglei Guo, Guozhe Meng. Design and Application of Bionic Surface for Directional Liquid Transportation [J]. Progress in Chemistry, 2022, 34(6): 1321-1336.
[10] Fangyuan Li, Junhao Li, Yujie Wu, Kaixiang Shi, Quanbing Liu, Hongjie Peng. Design and Preparation of Electrode Nanomaterials with “Yolk-Shell”Structure for Lithium/Sodium-Ion/Lithium-Sulfur Batteries [J]. Progress in Chemistry, 2022, 34(6): 1369-1383.
[11] Shiyu Li, Yongguang Yin, Jianbo Shi, Guibin Jiang. Application of Covalent Organic Frameworks in Adsorptive Removal of Divalent Mercury from Water [J]. Progress in Chemistry, 2022, 34(5): 1017-1025.
[12] Xiaoqing Ma. Graphynes for Photocatalytic and Photoelectrochemical Applications [J]. Progress in Chemistry, 2022, 34(5): 1042-1060.
[13] Xiuli Shao, Siqi Wang, Xuan Zhang, Jun Li, Ningning Wang, Zheng Wang, Zhongyong Yuan. Fabrication and Application of MFI Zeolite Nanosheets [J]. Progress in Chemistry, 2022, 34(12): 2651-2666.
[14] Xueer Cai, Meiling Jian, Shaohong Zhou, Zefeng Wang, Kemin Wang, Jianbo Liu. Chemical Construction of Artificial Cells and Their Biomedical Applications [J]. Progress in Chemistry, 2022, 34(11): 2462-2475.
[15] Baoyou Yan, Xufei Li, Weiqiu Huang, Xinya Wang, Zhen Zhang, Bing Zhu. Synthesis of Metal-Organic Framework-NH2/CHO and Its Application in Adsorption Separation [J]. Progress in Chemistry, 2022, 34(11): 2417-2431.