Back to Search
Start Over
Investigation of perinone compounds
- Source :
- Chemistry of Heterocyclic Compounds. 6:1326-1328
- Publication Year :
- 1970
- Publisher :
- Springer Science and Business Media LLC, 1970.
-
Abstract
- The electronic nature of the substituent in naphthalic anhydride has a substantial effect on the isomeric composition of the naphthaloperinones formed in reactions with 1,8-naphthylenediamine. An electron-accepting substituent in the 4 position of naphthalic anhydride promotes predominant retention of the carbonyl group in the 1 position, while an electrondonating substituent promotes retention of the carbonyl group in the 8 position of the naphthalene ring. 10-Amino- and 11-amino-14H-benzo[4,5]isoquinolino[2,1-a]perimidin-14-ones were synthesized.
Details
- ISSN :
- 15738353 and 00093122
- Volume :
- 6
- Database :
- OpenAIRE
- Journal :
- Chemistry of Heterocyclic Compounds
- Accession number :
- edsair.doi...........8cd5665a9238b30cca7bf681bbfa58f0
- Full Text :
- https://doi.org/10.1007/bf00755089