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.

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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

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article

Stereoselective Synthesis of (Z)‐β‐Thioenamide from (Z)‐Enamide‐Iodines and Thiols under Mild Conditions

Lian-Mei Chen, Liang Hong
European Journal of Organic Chemistry
Synthesis and Reactivity of Sulfur-Containing Compounds
article

Stereoselective Synthesis of (Z)‐β‐Thioenamide from (Z)‐Enamide‐Iodines and Thiols under Mild Conditions

Lian-Mei Chen, Liang Hong
article en

Abstract

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.

European Journal of Organic ChemistryVol. 27(47)
Chengdu University (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 88%
Synthesis and Reactivity of Sulfur-Containing Compounds
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