## Abstract For Abstract see ChemInform Abstract in Full Text.
A new direction of ring expansion of 1,2-dialkyldiaziridines in the reactions with arylketenes
β Scribed by Alexander V. Shevtsov; Vera Yu. Petukhova; Yurii A. Strelenko; Konstantin A. Lyssenko; Ivan V. Fedyanin; Nina N. Makhova
- Book ID
- 119768107
- Publisher
- Royal Society of Chemistry
- Year
- 2003
- Tongue
- English
- Weight
- 150 KB
- Volume
- 13
- Category
- Article
- ISSN
- 0959-9436
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π SIMILAR VOLUMES
A derivative of the Wieland-Miescher ketone can selectively be converted into either regioisomeric ring-expanded lactam. The synthesis of the diastereomeric N-a-methylbenzyl oxaziridine derivatives determines the regiochemistry of the product lactam and additionally allows the separation of a racemi
## Abstract magnified image New reaction of diaziridine ring expansion resulting in diethyl 1,2,3,6βtetrahydropyrimidineβ4,5βdicarboxylate derivatives was discovered under the action of diethyl acetylenedicarboxylate on 1,2βdiβ and 1,2,3βtrialkyldiaziridines in ionic liquids. J. Heterocyclic Chem.,