9‐Azahomocubane

Author:

Fahrenhorst‐Jones Tyler1ORCID,Marshall David L.2ORCID,Burns Jed M.1ORCID,Pierens Gregory K.3ORCID,Van Meurs Derek P.4,Kong Dehui1ORCID,Bernhardt Paul V.1ORCID,Blanksby Stephen J.2ORCID,Savage G. Paul5ORCID,Eaton Philip E.4,Williams Craig M.1ORCID

Affiliation:

1. School of Chemistry and Molecular Biosciences University of Queensland Brisbane 4072 Queensland Australia

2. Central Analytical Research Facility and School of Chemistry and Physics Queensland University of Technology Brisbane 4000 Queensland Australia

3. Centre for Advanced imaging University of Queensland Brisbane 4072 Queensland Australia

4. Department of Chemistry University of Chicago Chicago Illinois 60637 USA

5. CSIRO Manufacturing Ian Wark Laboratory Melbourne 3168 Victoria Australia

Abstract

AbstractHomocubane, a highly strained cage hydrocarbon, contains two very different positions for the introduction of a nitrogen atom into the skeleton, e. g., a position 1 exchange results in a tertiary amine whereas position 9 yields a secondary amine. Herein reported is the synthesis of 9‐azahomocubane along with associated structural characterization, physical property analysis and chemical reactivity. Not only is 9‐azahomocubane readily synthesized, and found to be stable as predicted, the basicity of the secondary amine was observed to be significantly lower than the structurally related azabicyclo[2.2.1]heptane, although similar to 1‐azahomocubane.

Funder

Australian Research Council

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

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