Intermolecular Friedel–Crafts reaction catalyzed by InCl 3
M Kaneko, R Hayashi, GR Cook
Index: Kaneko, Miho; Hayashi, Ryuji; Cook, Gregory R. Tetrahedron Letters, 2007 , vol. 48, # 40 p. 7085 - 7087
Full Text: HTML
Citation Number: 25
Abstract
Our recent discovery that In (III) salts were able to activate halides catalytically under mild conditions for the intermolecular Friedel–Crafts cyclization prompted us to explore this highly efficient activation in intermolecular Friedel–Crafts reactions. The alkylation of p-xylene with allylic and benzylic halides was demonstrated under catalytic and mild condition to afford in some cases quantitative yields of the monoalkylated products without the need to employ ...
Related Articles:
[Maity, Arnab Kumar; Chatterjee, Paresh Nath; Roy, Sujit Tetrahedron, 2013 , vol. 69, # 2 p. 942 - 956]
[Sakai, Norio; Kawana, Keita; Ikeda, Reiko; Nakaike, Yumi; Konakahara, Takeo European Journal of Organic Chemistry, 2011 , # 17 p. 3178 - 3183]
[Kobayashi, Tomoshige; Rahman, Sheikh Maksudur Synthetic Communications, 2003 , vol. 33, # 22 p. 3997 - 4003]
The synthetic potential of graphite-catalyzed alkylation
[Sereda, Grigoriy A.; Rajpara, Vikul B.; Slaba, Ryan L. Tetrahedron, 2007 , vol. 63, # 34 p. 8351 - 8357]
[Nishimoto, Yoshihiro; Babu, Srinivasarao Arulananda; Yasuda, Makoto; Baba, Akio Journal of Organic Chemistry, 2008 , vol. 73, # 23 p. 9465 - 9468]