Palladium (0)-catalyzed arylation of olefins by arylamines and an alkyl nitrite
K Kikukawa, K Maemura, Y Kiseki, F Wada…
Index: Kikukawa, Kiyoshi; Maemura, Koji; Kiseki, Yasuyuki; Wada, Fumio; Matsuda, Tsutomu; Giam, Choo S. Journal of Organic Chemistry, 1981 , vol. 46, # 24 p. 4885 - 4888
Full Text: HTML
Citation Number: 64
Abstract
Various olefins were arylated by the combination of arylamines and tert-butyl nitrite under palladium catalysis in the presence of acid such as monochloroacetic or acetic. The reaction proceeded in good yields without serious effects from substituents on either the olefinic substrates or the arylamines, including 3-aminopyridine.
Related Articles:
Alder-ene reaction of aryne with olefins
[Chen, Zhao; Liang, Jinhua; Yin, Jun; Yu, Guang-Ao; Liu, Sheng Hua Tetrahedron Letters, 2013 , vol. 54, # 43 p. 5785 - 5787]
[Kikukawa, Kiyoshi; Naritomi, Masaki; He, Gong-Xin; Wada, Fumio; Matsuda, Tsutomu Journal of Organic Chemistry, 1985 , vol. 50, # 3 p. 299 - 301]
[Sekine, Masaki; Ilies, Laurean; Nakamura, Eiichi Organic Letters, 2013 , vol. 15, # 3 p. 714 - 717]
[Berthiol, Florian; Doucet, Henri; Santelli, Maurice Tetrahedron Letters, 2003 , vol. 44, # 6 p. 1221 - 1225]
Arylation of olefins by arylazo aryl sulfones under palladium (0) catalysis.
[Kamigata, Nobumasa; Satoh, Akira; Kondoh, Tetsuya; Kameyama, Masayuki Bulletin of the Chemical Society of Japan, 1988 , vol. 61, p. 3575 - 3580]