Sammanfattning
Z-Ligustilide, a naturally occurring phthalide isolated from Ligusticum porteri, underwent Diels-Alder reactions with different dienophiles yielding novel tricyclic products with potentially interesting biological properties. Where selectivity was possible, the reactions performed showed regio- and stereoselectivity. The experimental results with ethyl acrylate were compared with the selectivity predicted by ab initio calculations.
Originalspråk | engelska |
---|---|
Sidor (från-till) | 4215-4218 |
Tidskrift | Tetrahedron Letters |
Volym | 48 |
Nummer | 24 |
DOI | |
Status | Published - 2007 |
Bibliografisk information
The information about affiliations in this record was updated in December 2015.The record was previously connected to the following departments: Organic chemistry (S/LTH) (011001240)
Ämnesklassifikation (UKÄ)
- Organisk kemi