Ferrous ion catalysis of reactions of nucleophiles with aryl halides
C Galli, JF Bunnett
Index: Galli, Carlo; Bunnett, J. F. Journal of Organic Chemistry, 1984 , vol. 49, # 16 p. 3041 - 3042
Full Text: HTML
Citation Number: 43
Abstract
Sir: In the recent decade it has been demonstrated in several instances that plain aryl halides, without elec- tron-attracting activating substituents, often react very satisfactorily with nucleophiles providing that reaction is appropriately provoked. Of major interest among such processes are reactions that occur by the radical chain SRNl mechanism.2 The propagation cycle for this mechanism is shown in Scheme I. Scheme I ... Although this mechanism ...
Related Articles:
[Gudla, Vanajakshi; Balamurugan, Rengarajan Tetrahedron Letters, 2012 , vol. 53, # 39 p. 5243 - 5247]
[Kosugi, Masanori; Hagiwara, Isao; Sumiya, Takashi; Migita, Toshihiko Journal of the Chemical Society, Chemical Communications, 1983 , # 7 p. 344 - 345]
[Nishiyama, Yutaka; Inoue, Jun; Teranishi, Kazuyo; Moriwaki, Masami; Hamanaka, Sawako Tetrahedron Letters, 1992 , vol. 33, # 42 p. 6347 - 6350]
[Piazza, Claudia; Millot, Nicolas; Knochel, Paul Journal of Organometallic Chemistry, 2001 , vol. 624, # 1-2 p. 88 - 95]
[Kuwajima, Isao; Urabe, Hirokazu Journal of the American Chemical Society, 1982 , vol. 104, # 24 p. 6831 - 6833]