Stereoselective Synthesis of (<i>Z</i>)‐β‐Thioenamide from (<i>Z</i>)‐Enamide‐Iodines and Thiols under Mild Conditions
Abstract The ( Z )‐β‐thioenamides is a valuable motif in many drugs. However, it's stereoselective synthesis is still facing challenge. Herein, we firstly reported a general and efficient approach for highly stereoselective synthesis of them by using ( Z )‐enamide‐iodines with thiols under transition metal‐free conditions.
Authors
- Lian-Mei Chen
- Liang Hong (ORCID: https://orcid.org/0000-0001-8955-6694)
Institutions
- Chengdu University (CN)
Publication Details
- Journal
- European Journal of Organic Chemistry
- Published
- 2024-09-22
- DOI
- https://doi.org/10.1002/ejoc.202400883
- Primary Topic
- Synthesis and Reactivity of Sulfur-Containing Compounds
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Natural Science Foundation of China