1-Acetyl-2-bromo-3-indolinone in nucleophilic substitution reactions and the synthesis of pyrrolo [3, 2-b] indoles
…, AI Mel'man, YI Smushkevich, VI Pol'shakov…
Index: Velezheva, V. S.; Mel'man, A. I.; Smushkevich, Yu. I.; Pol'shakov, V. I.; Anisimova, O. S. Pharmaceutical Chemistry Journal, 1990 , vol. 24, # 12 p. 917 - 923 Khimiko-Farmatsevticheskii Zhurnal, 1990 , vol. 24, # 12 p. 46 - 51
Full Text: HTML
Citation Number: 2
Abstract
Indoles with 2, 3-disubstitution and heterocycles obtained from them are of interest in the search for new biologically active materials [4, 9]. One of the possible approaches to the synthesis of compounds of such structure is in the use of 2-substituted indoxyls [i, 6]. The present work presents a new method for the introduction of nucleophilic substituents into position 2 of indoxyl and its subsequent conversion into hetero [b] indoles, and in ...
Related Articles:
Oxidation of indoles and 1, 2-dihydro-3H-indol-3-ones
[Desarbre; Savelon; Cornec; Merour Tetrahedron, 1996 , vol. 52, # 8 p. 2983 - 2994]
Total synthesis of (+)-isatisine A
[Kawasaki, Tomomi; Chien, Chun-Sheng; Suzuki, Takako; Takanami, Toshikatsu; Sakamoto, Masanori Heterocycles, 1985 , vol. 23, # 1 p. 172]