Issue 19, 2013

Hyperconjugation involving strained carbon–carbon bonds. Application of the variable oxygen probe to ester and ether derivatives of cubylmethanol

Abstract

Application of the variable oxygen probe to derivatives of (4-methoxycarbonyl)cubylmethanol 11 demonstrated a strong response of C–OR bond distance to the electron demand of the OR substituent, consistent with an enhanced σ-donor ability of the strained C–C bonds of cubane. The extent of cubane donor ability was found to be superior to an unstrained donor 13, comparing data extracted from the Cambridge Structural Database (T. W. Cole, Ph.D. Dissertation, University of Chicago, 1966), but weaker than the previously studied cyclopropane donors. Structural evidence is also found for σCC–π*CO interactions in these structures.

Graphical abstract: Hyperconjugation involving strained carbon–carbon bonds. Application of the variable oxygen probe to ester and ether derivatives of cubylmethanol

Supplementary files

Article information

Article type
Paper
Submitted
08 Feb 2013
Accepted
14 Mar 2013
First published
14 Mar 2013

Org. Biomol. Chem., 2013,11, 3151-3158

Hyperconjugation involving strained carbon–carbon bonds. Application of the variable oxygen probe to ester and ether derivatives of cubylmethanol

B. Harris, G. P. Savage and J. M. White, Org. Biomol. Chem., 2013, 11, 3151 DOI: 10.1039/C3OB40288F

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