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 1994; 1994(2): 125-126
DOI: 10.1055/s-1994-22764
DOI: 10.1055/s-1994-22764
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.
Intramolecular Hetero-Diels-Alder Reaction of Prolinal-Derived N-Arylimines Lewis Acid-Dependent Reversal of the Diastereoselectivity
Further Information
Publication History
Publication Date:
22 March 2002 (online)
Intramolecular Lewis acid-catalyzed hetero-Diels-Alder reaction of L-prolinal-derived N-arylimine 1 yielded diastereoselectively either the cis,cis-diazacyclopenta[a]anthracene derivative 2a or the trans,trans-isomer 2b, depending on the Lewis acid.