Base-assisted carbon-Claisen rearrangement of 4-phenyl-1-butene
M Newcomb, RS Vieta
Index: Newcomb, Martin; Vieta, Rene S. Journal of Organic Chemistry, 1980 , vol. 45, # 23 p. 4793 - 4795
Full Text: HTML
Citation Number: 7
Abstract
The [3, 3] sigmatropic rearrangements of all carbon systems in which one unsaturated site is constrained within an aromatic ring are poorly understood despite the fact that such rearrangements are related to both the Cope and Claisen rearrangements. No conversion of 4-phenyl-lbutene (1) to 3-(o-tolyl) propene (2) was observed in the
Related Articles:
[Littke, Adam F.; Schwarz, Lothar; Fu, Gregory C. Journal of the American Chemical Society, 2002 , vol. 124, # 22 p. 6343 - 6348]
[Chahdoura, Faouzi; Pradel, Christian; Gomez, Montserrat Advanced Synthesis and Catalysis, 2013 , vol. 355, # 18 p. 3648 - 3660]
[Ueno, Masahiro; Wheatley, Andrew E. H.; Kondo, Yoshinori Chemical Communications, 2006 , # 33 p. 3549 - 3550]
[Rao Volla, Chandra M.; Dubbaka, Srinivas Reddy; Vogel, Pierre Tetrahedron, 2009 , vol. 65, # 2 p. 504 - 511]
[Kayaki, Yoshihito; Koda, Takashi; Ikariya, Takao European Journal of Organic Chemistry, 2004 , # 24 p. 4989 - 4993]