Lewis Acid Promoted Highly Diastereoselective Desymmetric Intramolecular Cyclization of Allylstannane with a Diketone. -The prochiral allylstannyl diketone (I) undergoes Lewis acid catalyzed desymmetric intramolecular cyclization. By proper choice of the Lewis acid a highly diastereoselective synth
โฆ LIBER โฆ
ChemInform Abstract: Highly Diastereoselective 5-Hexenyl Radical Cyclizations with Lewis Acids and Carbohydrate Scaffolds.
โ Scribed by Eric J. Enholm; Jennifer S. Cottone; Florent Allais
- Publisher
- John Wiley and Sons
- Year
- 2001
- Weight
- 30 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0931-7597
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