An improved synthesis of 1,3,3-trimethyl-2-azabicyclo[2.2.2]octane and its nitroxyl radical product, A rigid analogue of TEMPO Full article
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Liebigs Annales
ISSN: 0947-3440 |
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| Output data | Year: 1997, Number: 7, Pages: 1587-1588 Pages count : 2 DOI: 10.1002/jlac.199719970740 | ||
| Tags | Limonene; Nitrogen heterocycles; Nitroxyl radicals; Steric hindrance; Terpenoids | ||
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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. © VCH Verlagsgesellschaft mbH, 1997.
Cite:
Bakunov S.
, Tkachev A.
An improved synthesis of 1,3,3-trimethyl-2-azabicyclo[2.2.2]octane and its nitroxyl radical product, A rigid analogue of TEMPO
Liebigs Annales. 1997. N7. P.1587-1588. DOI: 10.1002/jlac.199719970740 WOS Scopus РИНЦ OpenAlex
An improved synthesis of 1,3,3-trimethyl-2-azabicyclo[2.2.2]octane and its nitroxyl radical product, A rigid analogue of TEMPO
Liebigs Annales. 1997. N7. P.1587-1588. DOI: 10.1002/jlac.199719970740 WOS Scopus РИНЦ OpenAlex
Dates:
| Published print: | Jul 1, 1997 |
Identifiers:
| Web of science: | WOS:A1997XK28000038 |
| Scopus: | 2-s2.0-1842573496 |
| Elibrary: | 14874251 |
| OpenAlex: | W2059937473 |