# First Total Synthesis of Pestasulfamides A and B Through Iminoketene Dimerization of Anthranilic Acid in One-Pot Manner

## TL;DR

Scientists synthesized two natural compounds, pestasulfamides A and B, using a one-pot method involving a novel dimerization reaction.

## Contribution

The first total synthesis of pestasulfamides A and B using iminoketene dimerization of anthranilic acid in a one-pot process.

## Key findings

- Pestasulfamide A showed potent anti-acetylcholine esterase activity with an IC50 of 11.94 μM.
- A one-pot synthesis method was developed using sulfonylation-induced iminoketene dimerization.
- The method successfully produced both pestasulfamides A and B for the first time.

## Abstract

Pestasulfamides A and B are phenylbenzene-sulfonamides with an eight-membered dilactam, produced by mangrove endophytic fungus Pestalotiopsis sp. HNY36-1D. In bioassay, pestasulfamide A (1) exhibited potent anti-acetylcholine esterase (AChE) activities with an IC50 value of 11.94 μM, offering new pharmacophores with relevance to anti-Alzheimer’s disease drug discovery. Although the dimerization reaction of anthranilic acid derivatives forges an dibenzodiazocin-2,6-dione framework, the application of the dimerization to total synthesis of pestasulfamides A (1) and B (2) has not yet been realized. Herein, the first total synthesis of pestasulfamides A and B was achieved through one-pot protocol. The key step features a sulfonylation-induced iminoketene dimerization of anthranilic acid in a pyridine/THF system.