Abstract
The synthesis and the physical properties of some optically active 1,4-dialkylbuta-1,3-dienes are reported. The synthetic processes employed were essentially stereospecific. NMR, UV and CD spectra of these compounds provide information on the main conformation of the conjugated diene system, which was shown to be s-trans planar.
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.
