Porel, Mintu and Jayaraj, Nithyanandhan and Raghothama, S and Ramamurthy, V (2010) Chemistry in Confined Spaces: High-Energy Conformer of a Piperidine Derivative is Favored Within a Water-Soluble Capsuleplex. In: Organic Letters, 12 (20). pp. 4544-4547.
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Propyloxy-substituted piperidine in solution adopts a conformation in which its alkoxy group is equatorially positioned Surprisingly, two conformers of it that do not interconvert in the NMR time scale at room temperature have been found within an octa-acid capsule The serendipitous finding of the axial conformer of propyloxy-substituted piperidine within a supramolecular capsule highlights the value of confined spaces in physical organic chemistry.
|Item Type:||Journal Article|
|Additional Information:||Copyright of this article belongs to American Chemical Society.|
|Department/Centre:||Division of Chemical Sciences > NMR Research Centre (Formerly SIF)|
|Date Deposited:||26 Oct 2010 06:47|
|Last Modified:||26 Oct 2010 06:47|
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