## 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
ChemInform Abstract: The First Organocatalytic Enantio- and Diastereoselective 1,3-Dipolar Cycloaddition of Azomethine Ylides with Nitroalkenes.
β Scribed by Meng-Xia Xue; Xiao-Mei Zhang; Liu-Zhu Gong
- Publisher
- John Wiley and Sons
- Year
- 2008
- Weight
- 32 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0931-7597
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β¦ Synopsis
Abstract
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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