1,3-Dipolar Cycloaddition of Nitrones with 5-Methylenehydantoins: Synthesis and Transformation of New Spirohydantoin Derivatives
Author:
Affiliation:
1. a Laboratory of Asymmetric Organic Synthesis and Homogeneous Catalysis, Faculty of Sciences , Monastir, Tunisia
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
https://www.tandfonline.com/doi/pdf/10.1080/00397910903097237
Reference33 articles.
1. 1,3-Dipolar Cycloadditions. Past and Future
2. 1,3-Dipolar Cycloadditions of D-Erythrose- and D-Threose-Derived Alkenes with Nitrones
3. Regio- and Stereoselectivity of Captodative Olefins in 1,3-Dipolar Cycloadditions. A DFT/HSAB Theory Rationale for the Observed Regiochemistry of Nitrones
4. Investigations on Peri-, Regio- and Stereoselectivities in Thermal Cycloadditions Involving C -(4-Oxo-4 H [1]benzopyran-3-yl)- N -phenylnitrones: Role of Steric Factors and Secondary Interactions in 1,3-Dipolar Cycloadditions
5. Solution-phase parallel synthesis of highly diverse spiroisoxazolinohydantoins
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