Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5280525 | Tetrahedron Letters | 2007 | 4 Pages |
Abstract
The β-(trifluoromethyl)vinylsulfides on treatment with n-BuLi/TMEDA were readily lithiated at α-position of the sulfanyl group, and the generated α-lithiovinylsulfides were trapped with a variety of electrophiles to give the corresponding β-trifluoromethyl-α-functionalized vinylsulfides in good to high yields.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Takeshi Hanamoto, Ryoko Anno, Kenji Yamada, Kousuke Ryu,