Direct α‐Acylation of Thioesters With Carbonylimidazolides Toward α‐Substituted Malonate Monothioates and Weinreb‐Type Monoamides
A direct α‐acylation strategy of thioesters for the synthesis of α‐substituted monothiomalonates and β‐thioester‐Weinreb amides is described. Using carbonylimidazolides as acylating agents under LiHMDS‐mediated conditions, the method provides efficient access to a broad range of previously inaccessible derivatives, including α‐aryl analogs, in high yields without stoichiometric coupling reagents. The utility of the approach is demonstrated through gram‐scale reactions and diverse downstream functionalizations .
Authors
- L Zhang
- X. Wang
- Xinyu Wang (ORCID: https://orcid.org/0000-0002-2074-7297)
- Hui Jin (ORCID: https://orcid.org/0000-0002-5379-0064)
- Yanrong Ma
- Xu Cao
Institutions
- Shenyang University of Chemical Technology (CN)
Publication Details
- Journal
- European Journal of Organic Chemistry
- Published
- 2026-02-24
- DOI
- https://doi.org/10.1002/ejoc.202500925
- Primary Topic
- Sulfur-Based Synthesis Techniques
- Type
- article
- Field-Weighted Citation Impact
- 0.00