Synthesis of Spirooxindoles Bearing Iminothiolactone Moiety from Morita-Baylis-Hillman Carbonates of Isatins and Phenyl Isothiocyanate
Author:
Affiliation:
1. Department of Chemistry and Institute of Basic Science; Chonnam National University; Gwangju 500-757 Korea
Funder
National Research Foundation of Korea (NRF)
Korea government
Publisher
Wiley
Subject
General Chemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/bkcs.11051/fullpdf
Reference53 articles.
1. Spirooxindoles: Promising scaffolds for anticancer agents
2. Recent advances in the synthesis of biologically active spirooxindoles
3. Organocatalytic Asymmetric Assembly Reactions: Synthesis of Spirooxindoles via Organocascade Strategies
4. Recent Advances in Asymmetric Organocatalytic Construction of 3,3′-Spirocyclic Oxindoles
5. Isatins As Privileged Molecules in Design and Synthesis of Spiro-Fused Cyclic Frameworks
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2. Synthesis of five‐ring‐fused azepinone derivatives from bis‐isatins via sequential 6π‐electrocyclic ring closure, ring expansion, and dehydrogenation process;Bulletin of the Korean Chemical Society;2023-01-08
3. Synthesis of Spirooxindoles Bearing 1, 3‐Oxathiolane ‐2‐thione Moiety From Isatin‐Derived Propargylic Alcohols;Bulletin of the Korean Chemical Society;2021-01-03
4. Synthesis of spirooxindoles bearing 2,3-(or 2,5-)dihydrothiophene-2-thione moiety via [3+2] annulation of carbon disulfide with Morita-Baylis-Hillman carbonates of isatins;Tetrahedron Letters;2018-04
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