EventsThe 4th International Electronic Conference on Synthetic Organic Chemistry
Event submissions
Published
with-doi10.3390/ecsoc-4-01878
This submission belongs to the session a. General Organic Synthesis of the event The 4th International Electronic Conference on Synthetic Organic Chemistry
Published date
11 Sep, 2000
Citation
Constanze Bergt, Georg Uray, trans -(9,10)-Dihydro-11-Aminoethanoanthracene-12-Carboxylic Acid (AMEAC), A New Synthon For ß-Peptides, in Proceedings of The 4th International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 2000, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-4-01878
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trans -(9,10)-Dihydro-11-Aminoethanoanthracene-12-Carboxylic Acid (AMEAC), A New Synthon For ß-Peptides

Georg Uray 1
Constanze Bergt 1
1. Institute of Chemistry, Karl-Franzens-University of Graz, Heinrichstrasse 28, A-8010 Graz (Austria)
Abstract
ß-Amino acids and their peptides have most recently found intense interest in the research community [1].Oligomers ("foldamers") of unnatural amino acids have a wide range of potential applications. They may adopt compact, specific conformations. They could be used to form helices, turns and sheets and develop new types of tertiary structures. Certainly short peptides of this type have potential pharmaceutical applications.
Keywords
n/a
Synthesis of 2-nitromethyl-5-nitro-1,2,3,4-tetrazole
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