✦ LIBER ✦
A new and efficient electrochemical ring opening of 7-oxanorbornene systems via a modified Ritter reaction: direct approach to bicyclic valienamine analogues
✍ Scribed by David Le Goanvic; Marie-Christine Lallemand; François Tillequin; Thierry Martens
- Book ID
- 104230945
- Publisher
- Elsevier Science
- Year
- 2001
- Tongue
- French
- Weight
- 62 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
Electrogenerated acids (EGA), produced by controlled potential electrolysis in acetonitrile at a platinum electrode, permitted the oxa-ring opening and the acetamidation of the 7-oxanorbornene system of 4. It opens in one step a new route to bicyclic valienamine analogues 3.