| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5281881 | Tetrahedron Letters | 2009 | 5 Pages |
Abstract
Various 3,6-disubstituted N-2-thienyl/aryl-indoles were prepared by a short synthetic strategy involving reaction of substituted 2,4-difluoro/dichloro-styrene epoxide with substituted 2-formylaminothiophene/N-formylaniline in the presence of a base followed by treatment with an acid.
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Hanumant B. Borate, Sangmeshwer P. Sawargave, Suleman R. Maujan,