Further insight into the reaction of electrogenerated o-quinone with amino-alcohols and amines. Products and mechanism
M Largeron, A Neudorffer, MB Fleury
Index: Largeron, Martine; Neudorffer, Anne; Fleury, Maurice-Bernard Journal of the Chemical Society. Perkin Transactions 2, 1998 , # 12 p. 2721 - 2727
Full Text: HTML
Citation Number: 12
Abstract
Using 2, 3, 4-trihydroxybenzophenone as the starting material, the reaction of the electrogenerated 3, 4-quinone with amino-alcohols and amines HC (R1, R2)–NH2 is suggested to proceed via an ionic mechanism that would involve a C (3) aminated carbinolamine intermediate and would afford, after dehydration, a 3, 4-iminoquinone species. The subsequent step would consist either of a transamination reaction, or of the ...
Related Articles:
[Orito, Kazuhiko; Hatakeyama, Takahiro; Takeo, Mitsuhiro; Uchiito, Shiho; Tokuda, Masao; Suginome, Hiroshi Tetrahedron, 1998 , vol. 54, # 29 p. 8403 - 8410]
[Li, Minyan; Yuecel, Baris; Adrio, Javier; Bellomo, Ana; Walsh, Patrick J. Chemical Science, 2014 , vol. 5, # 6 p. 2383 - 2391]
[Grirrane, Abdessamad; Corma, Avelino; Garcia, Hermenegildo Journal of Catalysis, 2009 , vol. 264, # 2 p. 138 - 144]
[Volckaerts, E.; Geise, H. J.; Daelmans, F. Bulletin des Societes Chimiques Belges, 1992 , vol. 101, # 6 p. 503 - 508]
[Li, Minyan; Yuecel, Baris; Adrio, Javier; Bellomo, Ana; Walsh, Patrick J. Chemical Science, 2014 , vol. 5, # 6 p. 2383 - 2391]