Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5283055 | Tetrahedron Letters | 2006 | 5 Pages |
Abstract
trans-Stilbene oxide was oxidatively converted to 2-phenyl-1,3-dioxanes with phenyltrimethylammonium tribromide in the presence of various 1,3-diols and a catalytic amount of SbBr3 in DMSO at room temperature. Aromatic 1,2-diol, such as hydrobenzoin, was similarly converted to 2-aryl-1,3-dioxane derivatives under the same reaction conditions.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Shinsei Sayama,