| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5231166 | Tetrahedron | 2007 | 18 Pages |
Abstract
The conjugate addition of homochiral lithium N-benzyl-N-(α-methylbenzyl)amide to a range of γ-tert-butyldimethylsilyloxy but-2-enoates and but-2-enamides, and subsequent enolate functionalisation followed by deprotection, allows access to a range of 3-substituted-4-amino-γ-butyrolactones.
Related Topics
Physical Sciences and Engineering
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Authors
Elin Abraham, Jason W.B. Cooke, Stephen G. Davies, Alan Naylor, Rebecca L. Nicholson, Paul. D. Price, Andrew D. Smith,