| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5269742 | Tetrahedron Letters | 2011 | 4 Pages |
Abstract
Vilsmeier's reagent treatment of substituted diphenacyl sulfides or diphenacyl disulfides has led to the formation of a series of benzfused 3-chlorothiophene-2-carbaldehydes by a Domino Vilsmeier-Haack reaction/ring closure sequence, opening a new route for the synthesis of 3-chlorobenzo[b]thiophene-2-carbaldehydes and their benzfused analogues. A plausible mechanism has been proposed.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
![Domino Vilsmeier-Haack/ring closure sequences: a facile synthesis of 3-chlorobenzo[b]thiophene-2-carbaldehydes](/preview/png/5269742.png "First Page Preview: Domino Vilsmeier-Haack/ring closure sequences: a facile synthesis of 3-chlorobenzo[b]thiophene-2-carbaldehydes")
Authors
Nidhin Paul, Shanmugam Muthusubramanian,