Please use this identifier to cite or link to this item:
https://www.um.edu.mt/library/oar/handle/123456789/24645| Title: | A new two steps synthesis of α-substituted γ-methyl γ-lactones from nitroalkanes |
| Authors: | Ballini, Roberto Bosica, Giovanna |
| Keywords: | Nitroalkanes -- Synthesis Chemistry, Analytic |
| Issue Date: | 1996 |
| Publisher: | Georg Thieme Verlag |
| Citation: | Ballini, R., & Bosica, G. (1996). A new two steps synthesis of α-substituted γ-methyl γ-lactones from nitroalkanes. Synlett, 11, 1115-1116. |
| Abstract: | α-Substituted γ-methyl γ-lactones are efficiently prepared, in two steps, by regiospecific Michael addition of nitroalkanes to methyl trans-4-oxo-2-pentenoate in MeCN/DBU followed by chemoselective reduction of the obtained enones with NiCl2⋅6H2O/NaBH4. By this method a variety of functionalized 3,5-disubstituted butyrolactones can be obtained. |
| URI: | https://www.um.edu.mt/library/oar//handle/123456789/24645 |
| Appears in Collections: | Scholarly Works - FacSciChe |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| ballini2000.pdf Restricted Access | 149.89 kB | Adobe PDF | View/Open Request a copy |
Items in OAR@UM are protected by copyright, with all rights reserved, unless otherwise indicated.