Abstract
A computational study of the reaction mechanism of aryl propiolates with various radicals is carried out employing DFT and coupled-cluster methods, such as coupled-cluster singles and doubles with perturbative triples [CCSD(T)].
Full Text 
Sign-in/Register to access full text options
Sign-in/Register to access full text options 
Paper version not known
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 call
