Abstract
2-Hydroxymethylindole reacts with l-dehydroascorbic acid under mild conditions to give (3 R,3a R,10c S)-3-[(1 S)-1,2-dihydroxyethyl]-3a,10c-dihydroxy-3a,5,6,10c-tetrahydrofuro[3′,4′:5,6]pyrano[3,4- b]indol-1(3 H)-one. Its tosyl derivative undergoes cyclization to form a pentacyclic ketal derivative.
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.
