- PII
- 10.31857/S0044460X24040028-1
- DOI
- 10.31857/S0044460X24040028
- Publication type
- Article
- Status
- Published
- Authors
- Volume/ Edition
- Volume 94 / Issue number 4
- Pages
- 469-488
- Abstract
- In the reactions of 1,3-dipolar cycloaddition of a twofold excess of aryl aldimines of glycine ethyl ester with diarylideneacetones and diarylidenecyclohexanones in the presence of silver acetate, the corresponding dipyrrolidinylketones were obtained. Diethyl 4,4′-carbonylbis(3,5-diarylpyrrolidine-2-carboxylates) obtained from diarylideneacetones undergo aromatization under the action of N-bromosuccinimide to form diethyl 4,4′-carbonylbis(3,5-diaryl-1H-pyrrole-2-carboxylates). The selectivity of the reactions and the structure of the products were determined using correlation NMR spectroscopy and X-ray diffraction analysis.
- Keywords
- 1,3-диполярное циклоприсоединение ароматизация диарилиденацетон диарилиденцилогексанон дипирролидинилкетон дипирролилкетон
- Date of publication
- 15.04.2024
- Year of publication
- 2024
- Number of purchasers
- 0
- Views
- 28
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