Abstract
A palladium-catalyzed aminocarbonylative cyclization of benzyl chlorides with 2-nitroaryl alkynes has been developed for the rapid construction of indole skeletons. The reaction utilized nitroarenes as the nitrogen source, Mo(CO)6 as both the CO surrogate and the reductant to furnish various indole derivatives in moderate to high yields.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: 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.