Abstract
AbstractThe carbon and proton NMR spectra of syn‐ and anti‐tricyclo[5.1.0.03,5]octanes and their dichlorocarbene CH bond insertion products were determined by conventional 1D and 2D methods. Partially relaxed proton spectroscopy was carried out in some instances to aid in the separation of badly overlapped multiplets. A detailed analysis of the spectra was carried out with the aid of a new equation relating both the torsion angles and the CCH angles to the vicinal proton coupling constants. These values were combined with molecular modeling to draw conclusions regarding the conformational preferences for these molecules.
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
