Small-Ring Compounds. XIII. The Mechanism of Racemization of Optically Active 2, 4-Dichloro-3-phenylcyclobutenone1
EF Jenny, JD Roberts
Index: Jenny; Roberts Journal of the American Chemical Society, 1956 , vol. 78, p. 2005,2009
Full Text: HTML
Citation Number: 32
Abstract
I Enolization of 1 does not occur readily. The compound gives no color with ferric chloride solution and shows no hydroxyl absorption in the infrared. 3 It dissolves in alkali, but acidification yields 2, 4-dichloro-3-phenyl-3-butenoic acid and complex prod~ cts.~ No reaction was noted in an attempt to convert I to 1-acetoxy-2, 4-dichloro-3- phenylcyclobutadiene with isopropenyl acetate in the presence of p-toluenesulfonic acid ...
Related Articles:
[Kamon, Hitomi; Aoki, Yutaro; Nakata, Norio; Ishii, Akihiko Bulletin of the Chemical Society of Japan, 2014 , vol. 87, # 2 p. 274 - 282]
[Fukushima, Masahiro; Takushima, Daiki; Satomura, Hideaki; Onodera, Gen; Kimura, Masanari Chemistry - A European Journal, 2012 , vol. 18, # 26 p. 8019 - 8023]
[Bejot, Romain; Tisserand, Steve; Li, De Run; Falck; Mioskowski, Charles Tetrahedron Letters, 2007 , vol. 48, # 22 p. 3855 - 3858]
[Bejot, Romain; Tisserand, Steve; Li, De Run; Falck; Mioskowski, Charles Tetrahedron Letters, 2007 , vol. 48, # 22 p. 3855 - 3858]
[Bejot, Romain; Tisserand, Steve; Li, De Run; Falck; Mioskowski, Charles Tetrahedron Letters, 2007 , vol. 48, # 22 p. 3855 - 3858]