Abstract
A preliminary theoretical calculation was performed on the photosensitized internal cycloaddition in non-conjugate dienes by using an ab initio SCF MO procedure. The result explains very reasonably the experiments; predominant parallel compound from 1,4-diene, cross compound from 1,5-diene, and the ratios of these parallel/cross products in both cases.
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.
