Abstract
The cyclopentadiene (Cp) hyperconjugative aromaticity on anomeric carbon of piperidines was studied using DFT method. The aromaticity indices showed that Cp has considerably enhanced cyclic conjugation in comparison with unsubstituted Cp.
Full Text 
Sign-in/Register to access full text options
Sign-in/Register to access full text options 
Published version (
Free)
Free) 
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
