Radini et al., 2016 - Google Patents
Synthesis and functionalization of some new pyridazino [4, 5-b] indole derivativesRadini et al., 2016
View PDF- Document ID
- 17127383614003408215
- Author
- Radini I
- El-Kashef H
- Haider N
- Farghaly A
- Publication year
- Publication venue
- ARKIVOC
External Links
Snippet
Starting from the indole-fused pyridazinone 5, a series of new pyridazino [4, 5-b] indoles of potential pharmaceutical interest (9-18), was prepared. Compounds 20 and 21 were obtained by nucleophilic displacement of the chlorine atom of 19. Thionation of the chloro …
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 N1=NC=C2C3=CC=CC=C3NC2=C1 0 title abstract description 11
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
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