A highly diastereoseleetive method for the synthesis of 3-substituted isoindolin-l-ones has been developed through application of a tricyclic lactam substrate as an N-acyliminium ion precursor. Ringopening of the tricyclic lactam with triethylsilane as hydride source generates the targets with up to
β¦ LIBER β¦
Structure of a highly substituted pyrazolidin-3-one
β Scribed by Johnson, A. T. ;Keszler, D. A. ;Perri, S. T. ;White, J. D.
- Book ID
- 114509243
- Publisher
- International Union of Crystallography
- Year
- 1992
- Tongue
- English
- Weight
- 441 KB
- Volume
- 48
- Category
- Article
- ISSN
- 0108-2701
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