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Synlett 1994; 1994(11): 925-928
DOI: 10.1055/s-1994-23050
DOI: 10.1055/s-1994-23050
letter
© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved. This journal, including all individual contributions and illustrations published therein, is legally protected by copyright for the duration of the copyright period. Any use, exploitation or commercialization outside the narrow limits set by copyright legislation, without the publisher's consent, is illegal and liable to criminal prosecution. This applies in particular to photostat reproduction, copying, cyclostyling, mimeographing or duplication of any kind, translating, preparation of microfilms, and electronic data processing and storage.
Enantioselective Synthesis of Novel Functionalised Prolines via [3 + 2] Cycloadditions of a Chiral Azomethine Ylid
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Publikationsverlauf
Publikationsdatum:
22. März 2002 (online)
![](https://www.thieme-connect.de/media/synlett/199411/lookinside/thumbnails/10.1055-s-1994-23050-1.jpg)
The chiral, stabilised azomethine ylid 2 derived from (S)-2-phenylglycinol underwent enantioselective [3 + 2] cycloaddition reactions with a variety of unactivated and monoactivated dipolarophiles. Cycloaddition products were successfully deprotected to give chiral, functionalised proline derivatives.