A Divergent Synthesis of Numerous Pyrroloiminoquinone Alkaloids Identifies Promising Antiprotozoal Agents DOI Creative Commons
Griffin L. Barnes, Nicholas L. Magann,

Daniele Perrotta

et al.

Journal of the American Chemical Society, Journal Year: 2024, Volume and Issue: 146(43), P. 29883 - 29894

Published: Oct. 16, 2024

On the basis of a streamlined route to pyrroloiminoquinone (PIQ) core, we made 16 natural products spread across four classes biosynthetically related alkaloid products, and multiple structural analogs, all in ≤8 steps longest linear sequence (LLS). The strategy features Larock indole synthesis as key operation five-step methoxy-PIQ intermediate. Critically, this compound was readily diverged via selective methylation either (or both) imine-like or pyrrole nitrogens, which then permitted further divergence by

Language: Английский

Synthesis of the Pentacyclic Core of Sanguinone B Enabled by Alkyne Functionalization DOI Creative Commons
Jonathan Farhi, Samir P. Rezgui, Hao Yu

et al.

Organic Letters, Journal Year: 2025, Volume and Issue: unknown

Published: May 15, 2025

Sanguinones A and B are recently isolated pyrroloiminoquinone alkaloids possessing a rare C4 carboxylic acid. We report synthetic approach toward the full carbon nitrogen pentacyclic core of sanguinone B, with correct oxidation at C4. Highlights this include application Larock/Buchwald-Hartwig annulation cascade to access key tricyclic intermediate alkyne functionalization using Rh(I) or Cu(I) catalysis hindered benzylic ketones.

Language: Английский

Citations

0

A Divergent Synthesis of Numerous Pyrroloiminoquinone Alkaloids Identifies Promising Antiprotozoal Agents DOI Creative Commons
Griffin L. Barnes, Nicholas L. Magann,

Daniele Perrotta

et al.

Journal of the American Chemical Society, Journal Year: 2024, Volume and Issue: 146(43), P. 29883 - 29894

Published: Oct. 16, 2024

On the basis of a streamlined route to pyrroloiminoquinone (PIQ) core, we made 16 natural products spread across four classes biosynthetically related alkaloid products, and multiple structural analogs, all in ≤8 steps longest linear sequence (LLS). The strategy features Larock indole synthesis as key operation five-step methoxy-PIQ intermediate. Critically, this compound was readily diverged via selective methylation either (or both) imine-like or pyrrole nitrogens, which then permitted further divergence by

Language: Английский

Citations

0