An Easy Stereoselective Access to β,γ-Aziridino α-Amino Ester Derivatives via Mannich Reaction of Benzophenone Imines of Glycine Esters with N-Sulfonyl α-Chloroaldimines-Reference-Cited by-同舟云学术

An Easy Stereoselective Access to β,γ-Aziridino α-Amino Ester Derivatives via Mannich Reaction of Benzophenone Imines of Glycine Esters with N-Sulfonyl α-Chloroaldimines

Published:2007-08-17 Issue:19 Volume:72 Page:7199-7206
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Kiss Loránd¹,Mangelinckx Sven¹,Sillanpää Reijo¹,Fülöp Ferenc¹,De Kimpe Norbert¹

Affiliation:

1. Department of Organic Chemistry, Faculty of Bioscience Engineering, Ghent University, Coupure Links 653, B-9000, Ghent, Belgium, Institute of Pharmaceutical Chemistry, University of Szeged, H-6701 Szeged, P.O. Box 427, Hungary, and Department of Chemistry, University of Jyväskylä, Fin-40351, Jyväskylä, Finland

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo0710634

Reference112 articles.

1. Exploring Ramachandran and Chi Space: Conformationally Constrained Amino Acids and Peptides in the Design of Bioactive Polypeptide Ligands

2. Conformationally rigid cyclic α-amino acids in the design of peptidomimetics, peptide models and biologically active compounds

3. Cyclic amino acid derivatives

4. The Chemistry of 2-Aminocycloalkanecarboxylic Acids

5. Application of alicyclic β-amino acids in peptide chemistry

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