| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5271942 | Tetrahedron Letters | 2010 | 5 Pages |
Abstract
A highly diastereoselective pyrrolidine-promoted dibromination of alkenes by combination of NBS and succinimide is presented. The pyrrolidine-mediated dibromination of alkenes is higly anti-selective and gives the corresponding products in moderate to high yields and up to >25:1 dr.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
