Baseninduzierte Acyloin??Umlagerung sterisch gehinderter p??Chinole

A Nishinaga, T Itahara, T Matsuura, S Berger…

Index: Nishinaga,A. et al. Chemische Berichte, 1976 , vol. 109, p. 1530 - 1548

Full Text: HTML

Citation Number: 32

Abstract

Abstract 4-R-2, 6-di-tert-butyl-substituierte p-Chinole 1 erleiden in Gegenwart von Basen die Acyloin-Umlagerung. Durch Wanderung von R zum benachbarten C-Atom des Ringes entstehen dabei in guten Ausbeuten die Hydrochinone 2 oder durch deren Autoxidation ...

Related Articles:

Photo-induced reactions—XVIII: The photochemical transformation of 4-hydroxy-and 4-acetoxy-2, 5-cyclohexadienones

[Matsuura,T.; Ogura,K. Tetrahedron, 1968 , vol. 24, p. 6167 - 6175]

Photo-induced reactions—XVIII: The photochemical transformation of 4-hydroxy-and 4-acetoxy-2, 5-cyclohexadienones

[Matsuura,T.; Ogura,K. Tetrahedron, 1968 , vol. 24, p. 6167 - 6175]

Photo-induced reactions—XVIII: The photochemical transformation of 4-hydroxy-and 4-acetoxy-2, 5-cyclohexadienones

[Matsuura,T.; Ogura,K. Tetrahedron, 1968 , vol. 24, p. 6167 - 6175]

More Articles...