| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5286077 | Tetrahedron Letters | 2005 | 4 Pages |
Abstract
Pyrrolidine-derived arylglycines have been synthesized via a diastereoselective Petasis boronic acid Mannich reaction. Use of hexafluoroisopropanol as a co-solvent dramatically reduces reaction times, providing a practical room temperature process.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Kausik K. Nanda, B. Wesley Trotter,