| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5233010 | Tetrahedron | 2005 | 8 Pages |
Abstract
The reaction of α-keto esters with cyclopent-2-enone catalyzed by tertiary-phosphine organocatalyst of diphenylmethylphosphine provides the corresponding Baylis-Hillman adducts in higher yields. While the similar reaction of α-keto esters with cyclopent-2-enone furnishes the corresponding aldol adducts in the presence of tertiary-amine organocatalyst of DBU.
Related Topics
Physical Sciences and Engineering
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Authors
Min Shi, Wen Zhang,