Synthesis of anion-radical salts by hydride transfer reactions
β Scribed by Gunzi Saito; Allan K. Colter
- Publisher
- Elsevier Science
- Year
- 1977
- Tongue
- French
- Weight
- 227 KB
- Volume
- 18
- Category
- Article
- ISSN
- 0040-4039
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π SIMILAR VOLUMES
Cyclopropanation is regarded as an important transformation in organic synthesis. [1] Synthesis of 3-azabicyclo-A C H T U N G T R E N N U N G [3.1.0]hexane structures has been of interest because compounds with these structures, for example, indolizomycin, [2] trovafloxacin, [3] duocarmycin, and CC-
Cyclopropyl radicals normally undergo complete thermodynamic equilibration of configuration before they react, e.g., with bromine in the Hunsdiecker reaction'. Incomplete equilibration is normally due to steric or cage effectsa, and to surface effects when cyclopropyl halides are reduced with metals