The Infona portal uses cookies, i.e. strings of text saved by a browser on the user's device. The portal can access those files and use them to remember the user's data, such as their chosen settings (screen view, interface language, etc.), or their login data. By using the Infona portal the user accepts automatic saving and using this information for portal operation purposes. More information on the subject can be found in the Privacy Policy and Terms of Service. By closing this window the user confirms that they have read the information on cookie usage, and they accept the privacy policy and the way cookies are used by the portal. You can change the cookie settings in your browser.
Dibenzothiophene dioxides, which are readily prepared through oxidation of the parent dibenzothiophenes, undergo nucleophilic aromatic substitution with anilines intermolecularly and then intramolecularly to yield the corresponding carbazoles in a single operation. The “aromatic metamorphosis” of dibenzothiophenes into carbazoles does not require any heavy metals. This strategy is also applicable...
Der Modus der oxidative Anellierung von Meso(diarylamino)porphyrinen hängt stark von der Struktur der Diarylaminogruppen ab. Verbrückte Diarylaminogruppen führen zur Anellierung von 3,5‐Di‐tert‐butylphenyl‐Ringen an den Porphyrinkern (blau), nichtverbrückte Diarylaminogruppen ergeben Aminophenylen‐anellierte Porphyrine mit Brückenkopf‐N‐Atomen (rot).
Set the date range to filter the displayed results. You can set a starting date, ending date or both. You can enter the dates manually or choose them from the calendar.