| Article ID | Journal | Published Year | Pages | File Type | 
|---|---|---|---|---|
| 5273807 | Tetrahedron Letters | 2009 | 4 Pages | 
Abstract
												A phosphine-catalyzed [3+3] annulation reaction of modified tert-butyl allylic carbonates with various alkylidenemalononitriles to form cyclohexenes was developed. The use of protic solvent is crucial in this reaction. When non-polar solvent, toluene or xylene, was used, only non-cyclized product was obtained.
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											![First Page Preview: Phosphine-catalyzed [3+3] annulation reaction of modified tert-butyl allylic carbonates and substituted alkylidenemalononitriles Phosphine-catalyzed [3+3] annulation reaction of modified tert-butyl allylic carbonates and substituted alkylidenemalononitriles](/preview/png/5273807.png)