Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5266842 | Tetrahedron Letters | 2011 | 4 Pages |
Abstract
An efficient and regioselective introduction method of 2-methylpyridines to the secondary position of Baylis-Hillman adducts has been developed. A base treatment of 2-methylpyridinium salt of Baylis-Hillman bromide generated N-allylenamine intermediate which underwent a facile 3-aza-Cope rearrangement under mild conditions to produce the product.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Hyun Seung Lee, Sangku Lee, Se Hee Kim, Jae Nyoung Kim,