Abstract
Abstract A simple qualitative procedure is outlined for the conformational analysis of cycloheptane derivatives with particular attention to the natural perhydroazulenes. The procedure allows discrimination amongst different configuration and conformational isomers on grounds of thermodynamic stability. Using this procedure it is possible, by analyzing the known reactions of each, to derive stereochemical structures for the sesquiterpenes lactucin, artabsin and arborescin, tenulin, balduilin, and helenalin.
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.
