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The structure of the hydrazones formed fromβ-dicarbonyl compounds under the conditions of the azo-coupling reaction

✍ Scribed by V. N. Drozd; V. I. Sheichenko; V. N. Postnov

Book ID
112421419
Publisher
Springer
Year
1965
Tongue
English
Weight
179 KB
Volume
14
Category
Article
ISSN
1573-9171

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The reaction of tetramethoxyethylene wit
The reaction of tetramethoxyethylene with β-dicarbonyl compounds
✍ P. Camps; J.M. Drudis 📂 Article 📅 1978 🏛 Elsevier Science 🌐 French ⚖ 129 KB

Tetranethoxyethylene (TIIE) is a highly nucleophilic alkene that reacts with methanol, malononitrile or benmic acid to give the addition products, pentaoethoxyethane, 1,2,2~trimethoxyethyltdenemalononitrile and 1,1,2,2-tetramethoxyethyl benxoate respectively'. Roreover, the last product decomposes t