Base-catalyzed equilibration of anancomeric cyanocyclohexanes demonstrates that replacement of cis-3,5-dimethyl holding groups with electron-withdrawing CF groups dramatically increases the proportion of the axial cyano isomer present at equilibrium. The CF groups exert an effect on the conformational energy of the cyano group worth about 0.6 kcal/mol. A nonclassical hydrogen bond between the axial CN group and the syn-axial hydrogens is a major contributor to the axial stability of the group.

Download full-text PDF

Source
http://dx.doi.org/10.1021/acs.orglett.7b03287DOI Listing

Publication Analysis

Top Keywords

hydrogen bond
8
axial cyano
8
cyano group
8
experimental demonstration
4
demonstration sizeable
4
sizeable nonclassical
4
nonclassical ch···g
4
ch···g hydrogen
4
bond cyclohexane
4
cyclohexane derivatives
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!