1,3-Dipolar Cycloaddition of Isatin-Derived Azomethine Ylides with 2H-Azirines: Stereoselective Synthesis of 1,3-Diazaspiro[bicyclo[3.1.0]hexane]oxindoles-Reference-Cited by-同舟云学术

1,3-Dipolar Cycloaddition of Isatin-Derived Azomethine Ylides with 2H-Azirines: Stereoselective Synthesis of 1,3-Diazaspiro[bicyclo[3.1.0]hexane]oxindoles

Published:2019-03-12 Issue:7 Volume:84 Page:4273-4281
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Angyal Anikó¹²,Demjén András¹,Harmat Veronika³,Wölfling János²,Puskás László G.¹,Kanizsai Iván¹^ORCID

Affiliation:

1. AVIDIN Ltd., Alsó kikötő sor 11/D, Szeged H-6726, Hungary

2. Department of Organic Chemistry, University of Szeged, Dóm tér 8, H-6720 Szeged, Hungary

3. Laboratory of Structural Chemistry and Biology, and MTA-ELTE Protein Modeling Research Group, Institute of Chemistry, Eötvös Loránd University, Pázmány P. sétány 1/A, H-1117 Budapest, Hungary

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.9b00242

Reference53 articles.

1. Therapeutic Potential of Spirooxindoles as Antiviral Agents

2. Spiroindolones, a Potent Compound Class for the Treatment of Malaria

3. Discovery of a New Class of Potent, Selective, and Orally Bioavailable CRTH2 (DP2) Receptor Antagonists for the Treatment of Allergic Inflammatory Diseases

4. Structure-Based Design of Potent Non-Peptide MDM2 Inhibitors

5. Molecular diversity of spirooxindoles. Synthesis and biological activity

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