𝔖 Bobbio Scriptorium
✦   LIBER   ✦

The one-electron oxidation of 2-methoxy-4,6-di-t-butylphenol

✍ Scribed by J. Petránek; J. Pilař; D. Doskočilova


Publisher
Elsevier Science
Year
1967
Tongue
French
Weight
187 KB
Volume
8
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

✦ Synopsis


In connection with a program directed toward the systematic study of red-ox behaviour of phenols substituted with bulky alkyl groups we wish to describe in this communication the oxidation of 2-methoxy-4,6-di-t-butylphenol involving a one-electron transfer. The oxidation was carried out by


📜 SIMILAR VOLUMES


Base-catalyzed decomposition of 3,5-di-t
✍ A. Nishinaga; K. Nakamura; T. Matsuura 📂 Article 📅 1978 🏛 Elsevier Science 🌐 French ⚖ 197 KB

In a previous paper,' we reported a novel base-catalyzed rearrangement of R-peroxyquinol esters derived from 2,6-di-t-butylphenols leading to quinoxyacetic acid derivatives, where the peroxy bond cleaves even below -60 "C. Nature of the peroxy bond cleavage has been remained n

New 1,1-amino hydroperoxides from regios
✍ A. Nishinaga; T. Shimizu; T. Matsuura 📂 Article 📅 1980 🏛 Elsevier Science 🌐 French ⚖ 223 KB

The oxygenation of 4-(N-arylmethyleneamino)-2,6-di-t-butylphenols with Co(Salpr), a five coordinate Co(I1) Schiff base complex, in CH2C12 results in the regioselective hydroperoxylation at the imino carbon to give N-(1-aryl-1-hydroperoxymethyl)-3,5-di-tbutyl-R-benzoquinone mnoimines, which give excl