Stereoselective synthesis of 3-amino-2-oxindoles from isatin imines: new scaffolds for bioactivity evaluation
Author:
Affiliation:
1. Department of Chemistry
2. U.G.C. Centre of Advance Studies in Chemistry
3. Guru Nanak Dev University
4. Amritsar
5. India
6. DAV University
7. Jalandhar
Abstract
3-Substituted-3-aminooxindole motifs constitute the core structure of a number of natural products and drug candidates.
Publisher
Royal Society of Chemistry (RSC)
Subject
General Chemical Engineering,General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2015/RA/C5RA06969F
Reference111 articles.
1. The Asymmetric Intramolecular Heck Reaction in Natural Product Total Synthesis
2. Pyrrolidinyl-Spirooxindole Natural Products as Inspirations for the Development of Potential Therapeutic Agents
3. Synthesis and Reactivity of C-Heteroatom-Substituted Aziridines
4. Catalytic Asymmetric Synthesis of Oxindoles Bearing a Tetrasubstituted Stereocenter at the C-3 Position
5. Recent progress in enantioselective synthesis of C3-functionalized oxindoles: rare earth metals take action
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