Abstract
The scope and limitations of a novel free radical chain process involving the addition of benzyl radicals to substituted allyl bromides were examined and extended to explore the effect of α-substitution on the allyl bromide (R′), and the use of pyrrolidine amides and oxazolidinone as activating substituents (Z) as the first steps toward the development of a stereoselective, radical-based C–C bond-forming reaction which is environmentally benign.
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.
