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An Improved Synthesis of 1,3,3-Trimethyl-2-azabicyclo[2.2.2]octane and Its Nitroxyl Radical Product, a Rigid Analogue of TEMPO

✍ Scribed by Bakunov, Stanislav ;Tkachev, Alexey


Publisher
John Wiley and Sons
Year
1997
Tongue
English
Weight
246 KB
Volume
1997
Category
Article
ISSN
0947-3440

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✦ Synopsis


Abstract

A new synthetic approach for the production of isoquinuclidine 6 from dipentene (rac‐limonene, 1) is described. The nitroxyl 5, a rigid analogue of TEMPO, has been prepared from 6 in 87% yield.


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The synthesis of deuterium labelled anal
✍ P. H. Buckley; J. P. Dickens; T. A. Harrow; R. Honeyman πŸ“‚ Article πŸ“… 1979 πŸ› John Wiley and Sons 🌐 French βš– 248 KB

The synthesis of three deuterated analogues[d4, d and d ,2]octane is described. The compounds prepared were of high isotopic purity and were used in metabolism and bioavailability studies.