| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5271688 | Tetrahedron Letters | 2013 | 6 Pages |
Abstract
Simple and efficient protocols for the construction of substituted indanes and oxazolines through intramolecular cyclization of β-hydroxyarylethanamide using trifluoromethanesulfonic acid and titanium tetrachloride in 1,2-dichloroethane respectively have been described. The selectivity due to different acid catalysts was explored and optimized to achieve good to excellent yield.
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