Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5304918 | Tetrahedron Letters | 2019 | 4 Pages |
Abstract
Two routes to the novel scalemic β-amino disulfide 7 have been developed from (S)-phenylglycine and (R)-styrene oxide. The β-amino disulfide 7 was used as a catalyst in the enantioselective addition of diethylzinc to aldehydes providing (R)-secondary alcohols in 39-80% ee.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
David A. Fulton, Colin L. Gibson,