𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Quinonimines and aminoquinones, the reaction products of 3,6-di(tert-butyl)-o-benzoquinone with primary and secondary amines

✍ Scribed by G. A. Abakumov; V. K. Cherkasov; T. N. Kocherova; N. O. Druzhkov; Yu. A. Kurskii; L. G. Abakumova


Publisher
Springer
Year
2006
Tongue
English
Weight
386 KB
Volume
55
Category
Article
ISSN
1573-9171

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


ChemInform Abstract: The Reactions of 3,
✍ V. N. Glushakova; N. A. Skorodumova; V. I. Nevodchikov; L. G. Abakumova; N. P. M 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 29 KB 👁 1 views

The Reactions of 3,6-Di-tert-butyl-1,2-benzoquinone and 3,6-Ditert-butylcatechol with tert-Butyl Hydroperoxide. -The reaction of the title quinone (I) as well as its corresponding catechol with tert-butyl hydroperoxide in aprotic solvents results in ring oxidation accompanied by ring expansion furn

The Reaction of 3,6-di-tert-butyl-o-benz
✍ Alexandr V. Piskunov; Aryna V. Lado; Georgy K. Fukin; Evgeny V. Baranov; Ludmila 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 276 KB

## Abstract The reduction of 3,6‐di‐__tert__‐butyl‐__o__‐benzoquinone with tin amalgam gives the different tin catecholate complexes. The use of polar solvents for this reaction leads to the formation of Cat~2~Sn · L~2~ species (where Cat—dianion of 3,6‐di‐__tert__‐butylcatechol, L = Et~2~O, THF, P

Cycloaddition reactions of cyclooctyne w
✍ W. Verboom; H. J. T. Bos 📂 Article 📅 2010 🏛 Elsevier Science 🌐 English ⚖ 606 KB

## Abstract Treatment of a solution of 9,10‐phenanthrenequinone **4** and cyclooctyne **2** in chloroform with boron trifluoride‐ether affords the quinoid α,β‐unsaturated ketone **5** with loss of carbon monoxide. Reaction of 3,5‐di‐__tert__‐butyl‐__o__‐benzoquinone **9** with cyclooctyne **2** giv