NBS-mediated elimination of β-keto sulfides to access enones and dienones
Author:
Affiliation:
1. Jiangsu Key Laboratory of Pesticide Science and Department of Chemistry, College of Sciences, Nanjing Agricultural University, Nanjing, Jiangsu, China
Abstract
Funder
Nanjing Agricultural University
Shuangchuang Program of Jiangsu Province
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2023/OB/D2OB02135H
Reference60 articles.
1. Michael addition of thiols to α-enones in ionic liquids with and without organocatalysts
2. Organocatalytic enantioselective Michael addition of thioacetic acid to enones
3. Enantioselective Michael Reactions of β, β-Disubstituted Nitroalkenes: A New Approach to β2,2-Amino Acids with Hetero-Quaternary Stereocenters
4. Highly Enantioselective Organocatalytic Sulfa-Michael Addition to α,β-Unsaturated Ketones
5. Organocatalytic Asymmetric Sulfa-Michael Addition of Thiols to 4,4,4-Trifluorocrotonates
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