| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 9614568 | Journal of Molecular Catalysis A: Chemical | 2005 | 6 Pages |
Abstract
Readily available sulfamide-amine alcohol 11 was found to be effective in catalyzing the enantioselective phenylacetylene addition to aromatic ketones without using another central metal, providing the chiral tertiary propargylic alcohols in good yields (up to 83%) and enantioselectivities (up to 83% e.e.).
Keywords
Related Topics
Physical Sciences and Engineering
Chemical Engineering
Catalysis
Authors
Jincheng Mao, Boshun Wan, Fan Wu, Shiwei Lu,