Polaroghic reduction of some c~uplexl product of acztyl acetone with aryl diazonium chloride takes place in a single Qelectron transfer, giving a diffusion controllcd irreversible waves in B.R. buffers of pH range 2-11.8. The re&ction in these compounds takes place at the -NH-N = C bond. Effect of v
✦ LIBER ✦
Studies on the O/C-Arylation of Cyclic β-Diketones with activated aryl fluorides
✍ Scribed by J. Deutsch; Prof. Dr. H.-J. Niclas
- Book ID
- 105354134
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- English
- Weight
- 411 KB
- Volume
- 335
- Category
- Article
- ISSN
- 1615-4150
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