| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5286989 | Tetrahedron Letters | 2005 | 5 Pages |
Abstract
Electrolysis of arylidene- or alkylidenemalononitriles and malonate in alcohol in an undivided cell in the presence of sodium halide as mediator results in the stereoselective formation of alkyl (1R,5R,6R)* 6-substituted 5-cyano-4,4-dialkoxy-2-oxo-3-azabicyclo[3.1.0]hexan-1-carboxylates in 50-70% yields.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
![Stereoselective electrocatalytic transformation of arylidene- or alkylidenemalononitriles and malonate into alkyl (1R,5R,6R)* 6-substituted 5-cyano-4,4-dialkoxy-2-oxo-3-azabicyclo[3.1.0]hexane-1-carboxylates](/preview/png/5286989.png "First Page Preview: Stereoselective electrocatalytic transformation of arylidene- or alkylidenemalononitriles and malonate into alkyl (1R,5R,6R)* 6-substituted 5-cyano-4,4-dialkoxy-2-oxo-3-azabicyclo[3.1.0]hexane-1-carboxylates")
Authors
Michail N. Elinson, Sergey K. Feducovich, Zoya A. Starikova, Anatolii N. Vereshchagin, Sergey V. Gorbunov, Gennady I. Nikishin,