Synthesis of Insect Sex Pheromones by Ligand-Free Iron-Catalyzed Alkyl–Allyl Cross-Coupling Involving α,ω-Difunctionalized Aliphatic Grignard Nucleophiles and Allyl Electrophiles
We disclose synthetic access to four insect sex pheromones, proceeding with a key alkyl-allyl disconnection achieved by a ligand-free cross-coupling between α,ω-difunctionalized aliphatic Grignard reagents bearing terminal alkoxides and allylic electrophiles, mediated by an air-stable and inexpensive iron precatalyst. The efficiency of the coupling is ensured by a combination of exo- or endogenous magnesium alkoxide additives and LiCl, enabling appreciable, mild conditions (low 1 mol % catalyst load, noncryogenic temperatures) and proceeding with near-complete stereoselectivity.
Authors
- Olivier Guerret
- Guillaume Lefèvre (ORCID: https://orcid.org/0000-0001-9409-5861)
- Virginie Liautard
- Eric Gayon
- Adrien Tintar
Institutions
- Airbus (France) (FR)
- Centre National de la Recherche Scientifique (FR)
- Chimie ParisTech - PSL (FR)
- Université Paris Sciences et Lettres (FR)
- Health & Life (Taiwan) (TW)
Publication Details
- Journal
- ACS Omega
- Published
- 2026-02-05
- DOI
- https://doi.org/10.1021/acsomega.6c00255
- Primary Topic
- Radical Photochemical Reactions
- Type
- article
- Field-Weighted Citation Impact
- 0.00