Abstract
AbstractA strategy has been devised for the stereoselective synthesis of hexahydroindeno[2,1‐c]pyran scaffolds through a domino cyclization of (E)‐3,5‐diphenylpent‐4‐en‐1‐ol with aldehydes using BF3⋅OEt2 at 70 °C. It is an approach for the construction of the indeno[2,1‐c]pyran skeleton in a one‐pot operation through a cascade cyclization.
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.
