Chemischer Informationsdienst. Organische Chemie
 1971
DOI: 10.1002/chin.197148209
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ChemInform Abstract: 2,3‐TRIMETHYLEN‐NORBORNAN‐ADAMANTAN‐UMLAGERUNG, SELEKTIVE HALOGENIERUNG VON ADAMANTAN UND 1‐METHYL‐ADAMANTAN

H. Hamill1,
Aziz Karim2,
M. Anthony McKervey3

Abstract: Die Bromierung des endo‐ oder exo‐Norbomans (I) liefert in Gegenwart von AlBr3 bei 0°C das Naphthalin (II) (29% Ausbeute) und die Adamantane (III) (23%) und (IV) (24%).

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