| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5274257 | Tetrahedron Letters | 2012 | 4 Pages |
Abstract
This work concerns the asymmetric additions of benzothiazole to a variety of N-tert-butanesulfinyl imines with excellent diastereoselectivities (d.r. up to >99:1). Amino alkoxyl lithium was the key additive to obtain the excellent diastereoselectivity. More functionalized 4-methyl-5-vinyl thiazole and alkyl imines which can isomerize to enamines are also compatible substrates to the present protocol.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Jinlong Zhang, Yuhong Yang, Mei Wang, Li Lin, Rui Wang,