| Article ID | Journal | Published Year | Pages | File Type | 
|---|---|---|---|---|
| 5223957 | Tetrahedron | 2010 | 8 Pages | 
Abstract
												Carbanions of 3-substituted-3-chloropropyl phenyl sulfones add to carbonyl groups of aldehydes to produce aldol type adducts that undergo 1,5-intramolecular substitution giving 2,3,5-trisubstituted tetrahydrofurans. The effect of substituents in the 3-position of these sulfones on the relative rates of 1,3-intramolecular substitution of the corresponding γ-chlorocarbanions and their intramolecular addition are disclosed.
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											Authors
												Agnieszka Brandt, Anna Wojtasiewicz, Marcin Ånieżek, MieczysÅaw MÄ
kosza, 
											