| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5281237 | Tetrahedron Letters | 2010 | 4 Pages |
Abstract
In the presence of Pd2(dba)3-Cy3P catalyst, IPr·HCl salt [IPr = 1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene], and Cs2CO3, N-propargylamides react with allyl carbonates to give 2,5-disubstituted oxazoles having homoallyl groups through the tandem cycloisomerization-allylation.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Akio Saito, Koichi Iimura, Yuji Hanzawa,