Abstract
In this issue of Chem Catalysis , Wang et al. report the synthesis of 1,1-cyclopropanediesters promoted by a D 2 -symmetric chiral amidoporphyrin catalyst. The carbene transfer from unsymmetrical diazomalonates to a large scope of challenging alkenes occurred with high stereocontrol thanks to the efficiency of Co(II)-based metalloradical catalytic system. In this issue of Chem Catalysis , Wang et al. report the synthesis of 1,1-cyclopropanediesters promoted by a D 2 -symmetric chiral amidoporphyrin catalyst. The carbene transfer from unsymmetrical diazomalonates to a large scope of challenging alkenes occurred with high stereocontrol thanks to the efficiency of Co(II)-based metalloradical catalytic system.
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.
