Abstract
AbstractIn this work, several alkenylated benzo[1,2‐b:4,5‐b′]dithiophene were synthesized by Pd‐catalyzed C−H functionalization of benzo[1,2‐b:4,5‐b′]dithiophene with various alkenes. This direct alkenylation took place regioselectively at the C‐2 position of the fused heterocycle. The obtained compounds were structurally characterized by NMR and MS spectroscopic methods. Moreover, DFT calculations have been employed to shed light on the regioselectivity of the reaction as well as on the geometry and electronic properties of the newly formed C=C double bonds.
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.
