Chiral Calcium Phosphate-Catalyzed Enantioselective Amination of 3-Aryl-2-oxindoles with Dibenzyl Azodicarboxylate
Author:
Affiliation:
1. Institute for Molecular Design and Synthesis, School of Pharmaceutical Science and Technology, Tianjin University, Tianjin 300072, P. R. China
2. School of Science, Zhejiang Sci-Tech University, Hangzhou, Zhejiang 310018, P. R. China
Funder
Central Committee of the Chinese Communist Party
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.2c00432
Reference83 articles.
1. Organocatalytic Asymmetric Assembly Reactions: Synthesis of Spirooxindoles via Organocascade Strategies
2. Recent progress in enantioselective synthesis of C3-functionalized oxindoles: rare earth metals take action
3. Catalytic Asymmetric Synthesis of Oxindoles Bearing a Tetrasubstituted Stereocenter at the C-3 Position
4. Asymmetric Syntheses of Oxindole and Indole Spirocyclic Alkaloid Natural Products
5. Pyrrolidinyl-Spirooxindole Natural Products as Inspirations for the Development of Potential Therapeutic Agents
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1. Highly diastereoselective Mannich reaction between 3‑amino oxindole Schiff base and oxindole ketimines–Direct and effective preparation of adjacent tetrasubstituted 3,3′-bisoxindole protected diamines;Tetrahedron Letters;2023-06
2. Enantioselective Benzylation and Allylation of a Crucial Synthon of 3-Amino Oxindole Schiff Base Promoted by a Cinchonidinium Phase Transfer Catalyst to Enable the Effective Preparation of Chiral Quaternary 3-Amino Oxindoles;The Journal of Organic Chemistry;2023-04-13
3. Chiral organophosphates as ligands in asymmetric metal catalysis;Organic Chemistry Frontiers;2023
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