Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5333173 | Tetrahedron Letters | 2008 | 4 Pages |
Abstract
A series of 2-heterosubstituted 1,3-oxathianes were synthesized and their reactivity toward a strong base, sec-butyllithium, was studied. It was shown that sec-butyllithium attacked 2-heterosubstituted 1,3-oxathianes in three different ways depending upon the heteroatom at C-2; the removal of the proton at C-2, the nucleophilic attack at the heteroatom, or the nucleophilic attack at C-2 took place.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Kaoru Fuji, Masaru Ueda, Kenzo Sumi, Eiichi Fujita,