Symmetric Urea-catalyzed Asymmetric Michael Addition of Thiols to β-Nitrostyrenes
Author:
Affiliation:
1. Department of Chemistry, Faculty of Science, Ibaraki University
2. Process Chemistry Laboratory, Astellas Pharma Inc.
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
http://www.journal.csj.jp/doi/pdf/10.1246/cl.140591
Reference24 articles.
1. Asymmetric organocatalytic reactions by bifunctional amine-thioureas
2. Asymmetric catalysis with bifunctional cinchona alkaloid-based urea and thiourea organocatalysts
3. Asymmetric Sulfa-Michael Additions
4. Squaramide–Tertiary Amine Catalyzed Asymmetric Cascade Sulfa-Michael/Michael Addition via Dynamic Kinetic Resolution: Access to Highly Functionalized Chromans with Three Contiguous Stereocenters
5. Enantio- and diastereoselective addition of thioacetic acid to nitroalkenes via N-sulfinyl urea catalysis
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1. Dft Study of the Possible Mechanisms for the Synthesis of Α-Cyanophosphonates from Β-Nitrostyrenes;2024
2. Amino Amide Organocatalysts for Asymmetric Michael Addition of β-Keto Esters with β-Nitroolefins;Bulletin of the Chemical Society of Japan;2019-03-15
3. Addition Reactions: Polar Addition;Organic Reaction Mechanisms · 2014;2018-01-05
4. Catalyst-free sulfa-Michael addition of pyrimidine-2-thiol to nitroolefins;Journal of Sulfur Chemistry;2017-08-28
5. Asymmetric Michael addition of thiols to β-nitrostyrenes using a novel phenylpyrrolidine-based urea catalyst;Tetrahedron Letters;2015-01
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