Abstract
The regioselectivity of the cyclopropanation of polyenes by cycloaddition of carbenes generated by catalyzed decomposition of diazoesters in the presence of Rh, Pd and Cu catalysts can be controlled to some extent by selecting proper reaction parameters. For a particular diene, the regioselectivity depends both on the catalyst and on the nature of the double-bond (conjugation, substitution). The cyclopropanation of trienes containing both a conjugated diene system and an isolated double bond is reported as an application of these reactions. The practical interest of the present study is further demonstrated by the synthesis of a pyrethroid precursor by the rhodium(II) carboxylates catalyzed-cyclopropanations of 1.1-dichloro-4-methyl-1, 3-pentadiene.
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.
