Direct ortho Iodination of β??and γ??Aryl Alkylamine Derivatives

…, JM Álvarez??Gutiérrez, A Ballesteros…

Index: Barluenga, Jose; Alvarez-Gutierrez, Julia M.; Ballesteros, Alfredo; Gonzalez, Jose M. Angewandte Chemie - International Edition, 2007 , vol. 46, # 8 p. 1281 - 1283

Full Text: HTML

Citation Number: 31

Abstract

Selective CÀH functionalization reactions allow the rapid modification of available molecular scaffolds. Organometallic and electrophilic processes serve as synthetic tools to this end. Selective electrophilic aromatic substitution at the ortho position remains elusive in the case of monosubstituted arenes. Therefore, ortho-substituted derivatives are prepared typically by indirect strategies. Arynes,[1] or the orthometalated species obtained upon the treatment ...

Related Articles:

A simple and economical synthetic route to p-ethynylaniline and ethynyl-terminated substrates

[Melissaris, Anastasios P.; Litt, Morton H. Journal of Organic Chemistry, 1994 , vol. 59, # 19 p. 5818 - 5821]

Switching reaction pathways of trifluoromethylated thiobenzanilides by choice of different oxidative systems

[Zhu, Jiangtao; Xie, Haibo; Li, Shan; Chen, Zixian; Wu, Yongming Journal of Fluorine Chemistry, 2011 , vol. 132, # 5 p. 306 - 309]

Switching reaction pathways of trifluoromethylated thiobenzanilides by choice of different oxidative systems

[Zhu, Jiangtao; Xie, Haibo; Li, Shan; Chen, Zixian; Wu, Yongming Journal of Fluorine Chemistry, 2011 , vol. 132, # 5 p. 306 - 309]

More Articles...