Abstract
The first total synthesis of veiutamine, a new type of pyrroroiminoquinone marine alkaloid bearing a p-hydroxybenzyl substituent at C-6, has been achieved. The key step of the synthesis is 6-selective functionalization of the 1,3,4,5-tetrahydropyrrolo[4,3,2- de]quinoline nucleus via N-Boc-directed lithiation.
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.
