Prolinamides containing 2-(2-aminocyclohexyl)phenols as highly enantioselective organocatalysts for aldol reactions
Author:
Affiliation:
1. TÜBITAK Marmara Research Center, 41470 Gebze, Kocaeli, Türkiye
2. Department of Chemistry, Süleyman Demirel University, 32260 Isparta, Türkiye
3. TÜBITAK SAGE, 06261 Mamak, Ankara, Türkiye
Abstract
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2023/OB/D3OB00723E
Reference61 articles.
1. Catalytic enantioselective aldol reactions
2. Asymmetric synthesis of bicyclic intermediates of natural product chemistry
3. New Type of Asymmetric Cyclization to Optically Active Steroid CD Partial Structures
4. Proline-Catalyzed Direct Asymmetric Aldol Reactions
5. Kinetic and Stereochemical Evidence for the Involvement of Only One Proline Molecule in the Transition States of Proline-Catalyzed Intra- and Intermolecular Aldol Reactions
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1. Prolinamides derived from 2-aminocyclohexanols as organocatalysts for asymmetric List-Lerner-Barbas aldol reactions;Tetrahedron Letters;2024-04
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