Chemischer Informationsdienst
 1972
DOI: 10.1002/chin.197242138
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ChemInform Abstract: GEOMETRIE DES UEBERGANGSZUSTANDES BEI DER HYDOPEROX. VON MONOOLEFINEN MIT SINGULETT‐SAUERSTOFF

Alex Nickon1,
V. T. Chuang2,
Peter J. L. Daniels3
et al.

Abstract: Die Photooxidation des Olefins (I) in Pyridin bei 35°C in Gegenwart von Hämatoporphyrin liefert ein Hydroperoxid‐Gemisch, dessen Reduktion die Alkohole (II)‐(IV) im Verhältnis 57: 13:30 ergibt.

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