Design of polyaromatic hydrocarbon-supported tin reagents: A new family of tin reagents easily removable from reaction mixtures
D Stien, S Gastaldi
Index: Stien, Didier; Gastaldi, Stephane Journal of Organic Chemistry, 2004 , vol. 69, # 13 p. 4464 - 4470
Full Text: HTML
Citation Number: 32
Abstract
We report in this paper the preparation and use of stannanes 11, 12a, and 12b, compounds whose 3-pyrenylpropyl side chain affinity for activated carbon simplifies tin removal and product isolation. Our pyrene-supported reagents can be used for radical reductions and cyclizations (11), radical and cationic allylations (12a), and Stille couplings (12b) in much the same way as tributyltin derivatives.
Related Articles:
[Nithyanandhan, Jayaraj; Jayaraman, Narayanaswamy Tetrahedron, 2005 , vol. 61, # 47 p. 11184 - 11191]
[Niu, Jiajia; Guo, Pengran; Kang, Juntao; Li, Zhigang; Xu, Jingwei; Hu, Shaojing Journal of Organic Chemistry, 2009 , vol. 74, # 14 p. 5075 - 5078]
[Ogawa; Sumino; Nanke; Ohya; Sonoda; Hirao Journal of the American Chemical Society, 1997 , vol. 119, # 11 p. 2745 - 2746]
[Aki, Shinji; Nishi, Takao; Minamikawa, Jun-Ichi Chemistry Letters, 2004 , vol. 33, # 7 p. 940 - 941]
[Mathew, Siji; Divia; Nair, T.D. Radhakrishnan; Haridas, Karickal R. Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 2010 , vol. 49, # 10 p. 1389 - 1393]