| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5275078 | Tetrahedron Letters | 2008 | 5 Pages |
Abstract
An expeditious method to access 2-substituted benzimidazoles was developed. Both aromatic (phenols, anilines, and thiophenols) and alkyl nucleophiles (amines and thiols) react with 2-methylsulfonyl benzimidazole under solvent-free conditions to generate a variety of 2-substituted benzimidazoles.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Ping Lan, F. Anthony Romero, Threshia S. Malcolm, Benjamin D. Stevens, Dariusz Wodka, Gergely M. Makara,