Subscribe to RSS
Please copy the URL and add it into your RSS Feed Reader.
https://www.thieme-connect.de/rss/thieme/en/10.1055-s-00000083.xml
Synlett 1995; 1995(6): 647-649
DOI: 10.1055/s-1995-5015
DOI: 10.1055/s-1995-5015
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.
Efficient and Practical New Synthesis of 2-Oxazolines; 1,2-Bis- and 1,3-Bis(oxazolinyl)benzenes by [3+2] Cycloaddition Using Solvent-Free Conditions
Further Information
Publication History
Publication Date:
31 December 2000 (online)
![](https://www.thieme-connect.de/media/synlett/199506/lookinside/thumbnails/10.1055-s-1995-5015-1.jpg)
New 2-oxazolines, 1,2-bis- and 1,3-bis(oxazolinyl)benzenes were synthesized respectively from aliphatic, aromatic aldehydes, cinnamaldehyde, activated ketones, phthalic dicarboxaldehyde, isophthalaldehyde and imidate 1a derived from dimethyl aminomalonate by regioselective 1,3-dipolar cycloadditions using solvent-free conditions at 70°C.
[3+2] Cycloaddition - imidates - aldehydes - ketones - 2-oxazolines