Metal-Free Regioselective Oxa-Michael Approach to Access Spirooxindole-Fused Tetrahydrofuran/Tetrahydropyran through [3 + 2]/ [4 + 2] Spirocyclization of Methyleneindolinones with Haloalcohols-Reference-Cited by-同舟云学术

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Metal-Free Regioselective Oxa-Michael Approach to Access Spirooxindole-Fused Tetrahydrofuran/Tetrahydropyran through [3 + 2]/ [4 + 2] Spirocyclization of Methyleneindolinones with Haloalcohols

Published:2024-06-24 Issue:13 Volume:89 Page:9389-9404
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Savekar Amol T.¹,Gaikwad Ramesh A.¹,Waghmode Suresh B.¹^ORCID

Affiliation:

1. Department of Chemistry, Savitribai Phule Pune University (Formerly University of Pune), Ganeshkhind, Pune 411007, India

Funder

Council of Scientific and Industrial Research, India

Science and Engineering Research Board

University Grants Commission - South Eastern Regional Office

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.4c00659

Reference71 articles.

1. Spirooxindoles as Potential Pharmacophores

2. An overview of spirooxindole as a promising scaffold for novel drug discovery

3. Spirooxindoles: Promising scaffolds for anticancer agents

4. Natural Product-Derived Spirooxindole Fragments Serve as Privileged Substructures for Discovery of New Anticancer Agents

5. Enantioselective methodologies for the synthesis of spiro compounds

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