Synthesis and structure of 1-(2-amino)phenyl-2-phenyl-12H-indolo[3,2-c]carbazole ethylacetate solvate, a new indolocarbazole compound
β Scribed by Paolo Domiano; Vittorio Bocchi; Gerardo Palla
- Publisher
- Springer
- Year
- 1989
- Tongue
- English
- Weight
- 516 KB
- Volume
- 19
- Category
- Article
- ISSN
- 1572-8854
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## Abstract Novel __N__βsubstitutedβ3βaminoβ5βoxoβ4βphenylβ2,5βdihydroβ1__H__βpyrazoleβ1βcarbothioamide derivatives were synthesized by means of two methods. First is the cyclization reaction of 1β(cyanophenyl)acetylβ4βsubstituted thiosemicarbazide, and the second one is reaction of cyanophenyl ace
The title compound, CGS 148248, was synthesized with a '%-label in the azepine ring in 14 steps starting with l-bromo-3-phenylpropane (1> and K1%N in an overall yield of 1.31%. The reaction of I with K 1 k N yielded the nitrile 2 which upon hydrolysis followed by ring closure gave a-tetral~ne-l-~~c