Investigations of indolo[3,2-b]quinolines
✍ Scribed by N. Z. Tugusheva; S. Yu. Ryabova; N. P. Solov'eva; V. G. Granik
- Book ID
- 105534128
- Publisher
- Springer US
- Year
- 1998
- Tongue
- English
- Weight
- 340 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0009-3122
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
Investigations in Indolo[3,quinoline Series. -Several new 10-γaminoalkyl-substituted indoloquinolines [cf. (V) and (VI)] are prepared starting from 2-nitroindolo[3,2-b]quinoline (I). Raney-nickel catalyzed hydrogenation of the nitro group in starting compound (I) affords the 2-aminoindoloquinoline
## Abstract Treatment of 2‐hydroxy‐, 2‐mercapto‐, and 2‐ethoxycarbonylamino‐benzonitriles **12** with 2‐fluoro‐ or 2‐nitrophenacylbromides **13** under alkaline conditions provided the corresponding benzofuran, benzothiophene, and indole intermediates **10**, respectivelly. Nucleophilic cyclization
## Abstract For Abstract see ChemInform Abstract in Full Text.