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Solid-phase Synthesis of [4.4] Spirocyclic Oximes
Published on: February 6, 2019
Synthesis of Spirocyclic Indolenines
Michael J James1, Peter O'Brien1, Richard J K Taylor1
1Department of Chemistry, University of York, York, YO10 5DD, UK.
This review details synthetic methods for spirocyclic indolenines, which are important scaffolds. It covers interrupted Fischer indolisations, dearomatisation, and condensation reactions, offering historical context and future outlooks.
Area of Science:
- Organic Chemistry
- Synthetic Chemistry
Background:
- Spirocyclic indolenines are synthetically useful and biologically important scaffolds.
- Numerous synthetic methods have been developed over the past 77 years.
Purpose of the Study:
- To provide an in-depth review of spirocyclic indolenine synthesis.
- To categorize and discuss major synthetic strategies.
Main Methods:
- The review categorizes synthetic strategies into three main approaches:
- Interrupted Fischer indolisations
- Dearomatisation reactions of indoles
- Condensation reactions
Main Results:
- A wide array of diverse synthetic methods has been developed.
- The review examines the historical background, common synthetic challenges, and current state-of-the-art.
- Future perspectives in the field are also discussed.
Conclusions:
- The synthesis of spirocyclic indolenines is a dynamic field with a rich history.
- Continued development of synthetic strategies is expected.
- These scaffolds remain crucial in synthetic and medicinal chemistry.
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