## Abstract A number of 2,3‐pyrrolidinediones have been synthesised by the condensation of oxalacetic and oxalpropionic esters with different aldehydes and ketones. Typical reactions and properties of the diones have been studied by the preparation of suitable derivatives.
Heterocyclic compounds II: Synthesis and reactions of some 2,3-pyrrolidinediones
✍ Scribed by J. R. Merchant; Miss R. J. Shah; Miss R. M. Bhandarkar
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- English
- Weight
- 507 KB
- Volume
- 81
- Category
- Article
- ISSN
- 0165-0513
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
A number of 2,3‐pyrrolidinediones have been synthesised by the condensation of phenylpyruvic, 3,4‐dimethoxyphenylpyruvic and α‐keto‐butyric acid with different aldehydes and amines. In some cases, cinchoninic acids were the products of condensations. The properties and reactions of the pyrrolidinediones have been studied.
📜 SIMILAR VOLUMES
## Abstract For Abstract see ChemInform Abstract in Full Text.
## Abstract 3‐[(Trimethylsilylmethylamino)(methylthio)]methylene‐2‐coumaranone (**4a**) and 1‐methyloxindole (**4b**), readily prepared by reactions of the corresponding bis(methylthio)methylene heterocyclic compounds (**2a, b**), with (trimethylsilylmethyl)amine (3), were found to be synthetic equ