caa a22 4500 469050225 CHVBK 20180323132828.0 cr unu---uuuuu 170328e19920601xx s 000 0 eng 10.1007/BF02974089 doi (NATIONALLICENCE)springer-10.1007/BF02974089 Synthesis of benz[f] indole-4,9-dione Derivatives via intramolecular cyclization (II) [Elektronische Daten] [Myung-Eun Suh, Sang-Hee Shin] The new N-aryl-benz[f]-indole-4,9-dione derivatives were synthesizedvia intramolecular cyclization when triethylamine was employed as a base for the reaction of 2-chloro-3-(α-cyano-α-ethoxycarbonyl-methyl)-1,4-naphthoquinone and arylamines. The Pharmaceutical Society of Korea, 1992 2-amino-3-ethoxycarbonyl-N-(4-hydroxy-phenyl)-benz[f] indole-4,9-dione nationallicence 2-amino-3-ethoxycarbonyl-N-(4-methyl-phenyl)-benz[f] indole-4,9-dione nationallicence 2-amino-3-ethoxycarbonyl-N-(5-indanyl-phenyl)-benz[f] indole-4,9-dione nationallicence 2-amino-3-ethoxy-carbonyl-N-(4-amino-phenyl)-benz[f]-benz[f]-indole-4,9-dione nationallicence 2-amino-3-ethoxy-carbonyl-N-(3-hydroxyphenyl)-benz[f]-indole-4,9-dione nationallicence Suh Myung-Eun College of Pharmacy, Ewha Womans University, 120-750, Seoul, Korea aut Shin Sang-Hee College of Pharmacy, Ewha Womans University, 120-750, Seoul, Korea aut Archives of Pharmacal Research Pharmaceutical Society of Korea 15/2(1992-06-01), 138-141 0253-6269 15:2<138 1992 15 12272 https://doi.org/10.1007/BF02974089 text/html Onlinezugriff via DOI 1 research-article jats NATIONALLICENCE 856 40 https://doi.org/10.1007/BF02974089 text/html Onlinezugriff via DOI NATIONALLICENCE 700 1- Suh Myung-Eun College of Pharmacy, Ewha Womans University, 120-750, Seoul, Korea aut NATIONALLICENCE 700 1- Shin Sang-Hee College of Pharmacy, Ewha Womans University, 120-750, Seoul, Korea aut NATIONALLICENCE 773 0- Archives of Pharmacal Research Pharmaceutical Society of Korea 15/2(1992-06-01), 138-141 0253-6269 15:2<138 1992 15 12272 Metadata rights reserved Springer special CC-BY-NC licence nationallicence BK010053 XK010053 XK010000 NATIONALLICENCE NATIONALLICENCE NL-springer