Recently Tsutsumi and co-workers reported on the direct introduction of cyan0 groups into aromatic compounds by the electrolytic oxidation of inorganic cyanide in the presence of the aromatic compound (1). These workers found that
[2H] Labelling studies on the mechanism of electrocyclic aromatic substitution by the diazo-group
β Scribed by Thomas K. Miller; John T. Sharp; Gordon J. Thomas; Ian Thompson
- Publisher
- Elsevier Science
- Year
- 1981
- Tongue
- French
- Weight
- 219 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
β¦ Synopsis
A primary deuterium isotope effect has been observed in the cyclisation of diazocompounds (1) selectively deuteriated at the ring closure sites.
We have recently reported on the directive effects of meta substituents (R) in the synthesis of 1,2_benzodiazepines
(2) and (3) from B-aryl-a,B-unsaturated diazoalkanes (l).l
π SIMILAR VOLUMES
The 1,3 dipolar cycloadditions of diazomethane and ethyl diazoacetate with differently substituted 5-mlfur-2(5/-/)-furanones (1-6) are rcpone~ Cycloaddition of diazomethane occurs in a regio-and ~Β’ manner to give the ~ed adducts 9-14, in good yield. The cycloaddition with ethyl diazoat~ate occurs al