An Efficient and Diastereoselective Intramolecular 1,3-Dipolar Cycloaddition of Cyclic Azomethine Ylides and Nitrones.
โ Scribed by Rafael Pedrosa; Celia Andres; Javier Nieto; Cristobal Perez-Cuadrado; Ivan San Francisco
- Publisher
- John Wiley and Sons
- Year
- 2006
- Weight
- 19 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0931-7597
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
## Dedicated to Professor Wei-Yuan Huang on the occasion of his 85th birthday The 1,3-dipolar cycloaddition of azomethine ylides to electron-deficient alkenes is one of the most powerful methods for the construction of highly substituted pyrrolidine rings. [1] Following early research on the prepa
on the occasion of his 85th birthday The 1,3-dipolar cycloaddition of azomethine ylides to electron-deficient alkenes is one of the most powerful methods for the construction of highly substituted pyrrolidine rings. [1] Following early research on the preparation of optically active pyrrolidines in