# 2,3‐Epoxyamide‐alcohols in Domino Reactions: En Route to Molecular Diversity

## TL;DR

This paper introduces a new chemical method to create complex molecules with high stereochemical control using epoxyamides and domino reactions.

## Contribution

A novel domino reaction approach using 2,3-epoxyamides to synthesize diverse polycyclic lactams with full stereocontrol.

## Key findings

- Four different γ- and δ-lactam scaffolds were synthesized with good to high yields.
- Up to four contiguous stereocenters were fully controlled in the reaction products.
- The method offers high stereo- and chemoselectivity, enabling molecular diversity.

## Abstract

The synthesis of polycyclic γ‐ and δ‐lactams bearing up to four contiguous fully controlled stereocenters is presented. For that purpose, we developed an original approach based on the use of 2,3‐epoxyamides in domino reactions by taking advantage of the nucleophilic nitrogen atom and electrophilic epoxide. In reaction with enol ethers bearing gem bis‐electrophiles on the double bond as Michael acceptors, four different reaction pathways were observed. They all started with a domino oxa‐Michael/aza‐Michael/epoxide opening sequence and depending on substrates engaged could be followed either by a lactonization or a hemiketalization/retro‐aldol cascade. Thus, four original fully‐substituted piperidine‐ or pyrrolidine‐2‐one scaffolds were selectively synthesized in good to high yields. Moreover, these polycyclic lactams were obtained in high stereo‐ and chemo‐selectively highlighting the efficiency and molecular diversity offered by this new methodology that should offer various synthetic opportunities in the future.

Molecular diversity was achieved by reaction between easily accessible 2,3‐epoxyamido‐alcohols and Michael acceptors. 4 different γ‐ and δ‐lactam skeletons were selectively synthesized in good yields with up to 4 contiguous stereo‐centres fully controlled. Depending on the R substituent and the electron‐withdrawing groups different domino pathways, all triggered by an an oxa‐Michael/aza‐Michael/epoxide opening sequence, occurred.