Synthesis of Spirocyclopropane Oxindoles via Michael-Initiated Cyclopropanation of Pyridinium Salts with 3-Ylidene Oxindoles
Author:
Affiliation:
1. Advanced Research Institute and Department of Chemistry, Taizhou University
2. Department of Chemistry, Zhejiang Sci-Tech University
Abstract
Funder
Taizhou University
Publisher
Georg Thieme Verlag KG
Subject
Organic Chemistry
Link
http://www.thieme-connect.de/products/ejournals/pdf/10.1055/a-1327-6388.pdf
Reference3 articles.
1. Domino Corey–Chaykovsky Reaction for One-Pot Access to Spirocyclopropyl Oxindoles
2. Alkaloid inspired spirocyclic oxindoles from 1,3-dipolar cycloaddition of pyridinium ylides
3. Solvent-Controlled, Tunable Domino Reaction of 3-Ylideneoxindoles with in Situ-Generated α-Aryldiazomethanes: A Facile Access to 3-Spirocyclopropyl-2-oxindole and Pyrazoloquinazolinone Scaffolds
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1. The cyclization and functionalization reactions involving N-phenacylpyridinium salts;Chemical Papers;2024-07-07
2. DNA-Conjugated Cyclopropane Derivatives Constructed from Sulfonium Ylides with α,β-Unsaturated Ketones;Bioconjugate Chemistry;2023-08-17
3. New Synthetic Approaches to Benzo-Fused Spiro Heterocycles;Russian Journal of Organic Chemistry;2022-10
4. Synthesis and computational studies of potent antimicrobial and anticancer indolone scaffolds with spiro cyclopropyl moiety as a novel design element;Journal of the Indian Chemical Society;2022-07
5. Microwave induced formal [2 + 1] Michael-cyclization cascade sequence of 3-ylidene oxindoles and pyridinium phenacyl salts;Synthetic Communications;2022-06-15
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