Formal Syntheses of Dictyodendrins B, C, and E by a Multi-substituted Indole Synthesis

02 April 2021, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

The dictyodendrins are a family of marine alkaloids, which possess a highly substituted pyrrolo[2,3-c]carbazole core. This core structure can be regarded as a multi-substituted indole and aniline moiety. To achieve a concise synthesis of dictyodendrins, we planned to capitalize on our previously developed multi-substituted indole synthesis. By using this method along with two C–H functionalizations, formal syntheses of dictyodendrin B, C, and E were achieved.

Keywords

Total syntheses
Natural products
dictyodendrin
indole
C–H functionalization

Supplementary materials

Title
Description
Actions
Title
kabuki210401SIfinal
Description
Actions

Comments

Comments are not moderated before they are posted, but they can be removed by the site moderators if they are found to be in contravention of our Commenting Policy [opens in a new tab] - please read this policy before you post. Comments should be used for scholarly discussion of the content in question. You can find more information about how to use the commenting feature here [opens in a new tab] .
This site is protected by reCAPTCHA and the Google Privacy Policy [opens in a new tab] and Terms of Service [opens in a new tab] apply.