ChemInform Abstract: Reaction of Dihalocarbenes with N-Alkylidene Amino Acid Esters and Nitriles. Synthesis of Aziridine and Pyrrole Amino Acid Derivatives.
β Scribed by A. F. Khlebnikov; M. S. Novikov; T. Yu. Nikiforova; R. R. Kostikov
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 31 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0931-7597
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β¦ Synopsis
Reaction of Dihalocarbenes with N-Alkylidene Amino Acid Esters and Nitriles. Synthesis of Aziridine and Pyrrole Amino Acid Derivatives.
-The synthesis of functionalized dihaloaziridines [cf. (V), (VII), (IX)] by reaction of N-benzhydrylidene amino acid derivatives or benzophenone imine derivatives with dihalocarbenes is described. Proline derivative (X) does not give the expected aziridine derivative with dichlorocarbene but furnishes the bicyclic adduct (XII) in the presence of maleate. -(KHLEBNIKOV, A.
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The title esters (III) as well as their ammonium salts (V) are synthesized and tested for their cholinergic activity.