Synthesis of 3-acyl-5-hydroxyindoles and 3-acyl-5-hydroxybenzofurans. Influence of solvent on the course of the Nenitzescu reaction
TI Mukhanova, LM Alekseeva, EF Kuleshova…
Index: Mukhanova, T. I.; Alekseeva, L. M.; Kuleshova, E. F.; Sheinker, Yu. N.; Granik, V. G. Pharmaceutical Chemistry Journal, 1993 , vol. 27, # 2 p. 136 - 142 Khimiko-Farmatsevticheskii Zhurnal, 1993 , vol. 27, # 2 p. 60 - 65
Full Text: HTML
Citation Number: 2
Abstract
136 0091-150X/93/2702-0136512.50 9 1993 Plenum Publishin~ Corporation reaction. Thus the reaction of benzoquinone (I) with l-acetyl-2-amino-l-propene (IIa) leads to a mixture of 2- methyl-3-acetyl-5-hydroxyindole (III, R= H)(IIIa) and-benzofuran (IV)[5], but the use of the N- methyl (IIb) and N-ethyl derivatives of enaminoketone IIa gave only the benzofuran IV [3]. Conversely, treatment of quinone I with the corresponding N-aryl analogs (IIc and IId) ...
Related Articles:
[Thirupathaiah; Venkateshwar Rao; Ramanna Oriental Journal of Chemistry, 2010 , vol. 26, # 4 p. 1521 - 1524]
[Gadaginamath, Guru S.; Kavali, Rajesh R.; Pujar, Shashikanth R. Synthetic Communications, 2003 , vol. 33, # 13 p. 2285 - 2292]
[Struebe, Frank; Rath, Susann; Mattay, Jochen European Journal of Organic Chemistry, 2011 , # 24 p. 4645 - 4653]
[Struebe, Frank; Siewertsen, Ron; Soennichsen, Frank D.; Renth, Falk; Temps, Friedrich; Mattay, Jochen European Journal of Organic Chemistry, 2011 , # 10 p. 1947 - 1955]