Kupriyan, D. G. ; Anikin, V. F. ; Merz, A. ; Pantsenker, L. D.
Alternative Links zum Volltext:DOIVerlag
| Dokumentenart: | Artikel |
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| Titel eines Journals oder einer Zeitschrift: | Russian Journal of Organic Chemistry |
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| Verlag: | MAIK NAUKA/INTERPERIODICA/SPRINGER |
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| Ort der Veröffentlichung: | NEW YORK |
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| Band: | 40 |
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| Nummer des Zeitschriftenheftes oder des Kapitels: | 5 |
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| Seitenbereich: | S. 699-704 |
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| Datum: | 2004 |
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| Institutionen: | Chemie und Pharmazie > Institut für Organische Chemie |
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| Identifikationsnummer: | | Wert | Typ |
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| 10.1023/B:RUJO.0000043717.08167.c6 | DOI |
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| Stichwörter / Keywords: | LUMINESCENT PROPERTIES; NAPHTHALIC ANHYDRIDE; BIOLOGICAL-ACTIVITY; BIS-NAPHTHALIMIDES; ANTITUMOR AGENTS; DERIVATIVES; |
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| Dewey-Dezimal-Klassifikation: | 500 Naturwissenschaften und Mathematik > 540 Chemie |
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| Status: | Veröffentlicht |
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| Begutachtet: | Ja, diese Version wurde begutachtet |
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| An der Universität Regensburg entstanden: | Ja |
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| Dokumenten-ID: | 71616 |
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Zusammenfassung
The synthetic route to 4-substituted bisnaphthalimides consisting in reaction of 4-halonaphthalic anhydrides with alpha,omega-diaminoalkanes followed by halogen substitution with dialkylamino group is more promising than imidating coupling of 4-dialkylaminonaphthalic anhydrides for it opens wider synthetic opportunities and ensures better yields of target products. Dihalosubstituted ...
Zusammenfassung
The synthetic route to 4-substituted bisnaphthalimides consisting in reaction of 4-halonaphthalic anhydrides with alpha,omega-diaminoalkanes followed by halogen substitution with dialkylamino group is more promising than imidating coupling of 4-dialkylaminonaphthalic anhydrides for it opens wider synthetic opportunities and ensures better yields of target products. Dihalosubstituted bis-naphthalimides can be prepared by N-alkylation of the corresponding naphthalimides with polymethylene dibromides under conditions of phase-transfer catalysis in the presence of tetraalkylammonium salts.
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