A one step synthesis of 4-oxo-Δ2-pyrrolines from iminoesters
✍ Scribed by .P.C. Srivastava; C.M. Gupta; A.P. Bhaduri
- Book ID
- 104247684
- Publisher
- Elsevier Science
- Year
- 1971
- Tongue
- French
- Weight
- 116 KB
- Volume
- 12
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
Kjaer2 reported that the reaction of ethyl <-ethoxy-P-phenylethylideneaminoacetate (I: R = II) with morpholine led to the formation of unexpected products, and he proposed that the data could be best presented by structure 11 or III, However, on mechanistic consideration it was difficult to visualise the functionalisation of one of the morpholine methylenes under the mild experlmental conditions used and, therefore, the assigned structure II or II1 seemed untenable.
This prompted us to reinvestigate this reaction.
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## Abstract Novel 4‐amino‐6‐aryl‐2‐phenylpyrimidine‐5‐carbonitriles have been prepared in one step procedure from the readily available 4‐aryl‐2‐amino‐3‐cyano‐5,6,7,8‐tetrahydro‐7,7‐dimethyl‐5‐oxo‐4__H__‐benzopyrans. The mass spectroscopy study under EI conditions shows molecular peaks with high in
Acetoacetic ester is converted can be hydrolyzed to give tetramic acids. The 2,4-pyrrolidinedione nucleus (4)