Stereoselective Access to Azetidine-Based α-Amino Acids and Applications to Small Peptide Synthesis
Author:
Affiliation:
1. Department of Chemistry and Pharmacy, Ludwig-Maximilians-Universität München, Butenandtstraße 5-13, 81377 Munich, Germany
Funder
Deutsche Forschungsgemeinschaft
Ludwig-Maximilians-Universität München
Fonds der chemischen Industrie
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.0c03131
Reference38 articles.
1. Azetidine-2-Carboxylic Acid: a New Constituent of Plants
2. Structural Modification of a Periodic Polypeptide through Biosynthetic Replacement of Proline with Azetidine-2-carboxylic Acid
3. AF12198, a Novel Low Molecular Weight Antagonist, Selectively Binds the Human Type I Interleukin (IL)-1 Receptor and Blocks in Vivo Responses to IL-1
4. Misincorporation of the Proline Analog Azetidine-2-Carboxylic Acid in the Pathogenesis of Multiple Sclerosis: A Hypothesis
5. Synthesis of new functionalized aziridine-2- and azetidine-3-carboxylic acid derivatives of potential interest for biological and foldameric applications
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