## Abstract Analysis of the IR., UV., and polarographic data of a variety of 2‐arylhydrazono‐3‐ketimino‐nitriles indicated that these derivatives exist mainly in the intramolecularly chelated hydrazone structure **1**. Compounds **1** reacted with hydrazine hydrate to yield the corresponding 5‐ami
Reaction of the nitrile of 3,3-diphenyl-2-propenic acid with the carbanions of some α-branched nitriles Short communication
✍ Scribed by Kostadinka Popandova-Yambolieva; Christo Ivanov
- Book ID
- 105012002
- Publisher
- Springer Vienna
- Year
- 1979
- Tongue
- English
- Weight
- 159 KB
- Volume
- 110
- Category
- Article
- ISSN
- 0026-9247
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## Abstract magnified image 2‐Dimethylaminomethylene‐3‐oxo‐__N__‐phenylbutyramide **1** reacts with malononitrile **2a** to afford the pent‐2‐enedioic acid 1‐amide 5‐phenylamide derivative **6**, which could be cyclized to give the 6‐methylpyridone derivative **7**. Compound **1** reacts with cyan
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