| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5277912 | Tetrahedron Letters | 2007 | 4 Pages |
Abstract
Poly-substituted nitrobenzenes were synthesized from Baylis-Hillman adducts via the [3+3] annulation strategy as the key step. 1,3-Dinitroalkanes served as the 1,3-dinucleophilic component and the Baylis-Hillman acetates as a 1,3-dielectrophilic part.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
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Authors
Da Yeon Park, Ka Young Lee, Jae Nyoung Kim,