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Azabicyclic alcohols. VI. Azabicyclo [2.2.1]heptan-3-ol epimers

✍ Scribed by Spry, Douglas O.; Aaron, Herbert S.

Book ID
126075715
Publisher
American Chemical Society
Year
1969
Tongue
English
Weight
473 KB
Volume
34
Category
Article
ISSN
0022-3263

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πŸ“œ SIMILAR VOLUMES

ChemInform Abstract: Efficient Synthesis
ChemInform Abstract: Efficient Synthesis of exo-1-Azabicyclo(2.2.1)heptan-3-ol.
✍ S. D. BARRETT; J. C. JAEN; B. W. CAPRATHE; A. J. THOMAS; H. TECLE πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 30 KB πŸ‘ 1 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a β€œFull Text” option. The original article is trackable v

Absolute Configuration of 3-Substituted
Absolute Configuration of 3-Substituted 1-Azabicyclo[2.2.1]heptanes
✍ Jakob Boelsterli; Ursula Eggnauer; Esteban Pombo-Villar; Hans-Peter Weber; Malco πŸ“‚ Article πŸ“… 1992 πŸ› John Wiley and Sons 🌐 German βš– 396 KB

The l-azabicyclo[2.2. I]heptan-3-exo-ol (2) was resolved by fractional crystallisation of its hydrogen tartrate salts. The enantiomers (+)-and (-)-2 were oxidised to the ketones (-)-4 and (+)-4, respectively (Scheme). CD spectroscopy suggested that (-)-4 possesses the (IR,4S)-configuration. This abs