# Achmatowicz rearrangement-enabled unified total syntheses of (+)-passifetilactones A–C

## TL;DR

The paper describes a unified and efficient method to synthesize three natural products called passifetilactones A–C using a streamlined chemical process.

## Contribution

A unified synthetic strategy is introduced for passifetilactones A–C using Achmatowicz rearrangement and stereoselective catalytic transformations.

## Key findings

- A chiral furan-derived alcohol was synthesized using the Corey–Bakshi–Shibata reduction.
- The Achmatowicz rearrangement enabled construction of the α-hydroxy–δ-pyrone core.
- An iridium-catalyzed redox isomerization provided the δ-hydroxy-α-pyrone framework efficiently.

## Abstract

In this manuscript, we report the enantio- and diastereoselective total synthesis of three cytotoxic 2-pyrone-derived natural products passifetilactones A–C. Our strategy leverages a unified synthetic approach that originates from simple furan-based building blocks. Key transformations include the Corey–Bakshi–Shibata (CBS) reduction to access chiral furan-derived alcohol, NBS-mediated Achmatowicz rearrangement to construct the α-hydroxy–δ-pyrone core, followed by a highly stereoselective, iridium-catalyzed dynamic kinetic intramolecular redox isomerization to access the δ-hydroxy-α-pyrone framework. This streamlined route enables efficient access to passifetilactones A, B, and C in 13, 5, and 8 steps, with overall yields of 12%, 54%, and 37%, respectively.

In this manuscript, we report the enantio- and diastereoselective total synthesis of three cytotoxic 2-pyrone-derived natural products passifetilactones A–C.