Proline Derived Spirobarbiturates as Highly Effective β-Turn Mimetics Incorporating Polar and Functionalizable Constraint Elements-Reference-Cited by-同舟云学术

Proline Derived Spirobarbiturates as Highly Effective β-Turn Mimetics Incorporating Polar and Functionalizable Constraint Elements

Published:2008-03-26 Issue:9 Volume:73 Page:3608-3611
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Lomlim Luelak¹,Einsiedel Juergen¹,Heinemann Frank W.¹,Meyer Karsten¹,Gmeiner Peter¹

Affiliation:

1. Department of Chemistry and Pharmacy, Emil Fischer Center, Chair of Medicinal Chemistry, Friedrich Alexander University, Schuhstrasse 19, D-91052 Erlangen, Germany, and Department of Chemistry and Pharmacy, Chair of Inorganic Chemistry, Friedrich Alexander University, Egerlandstrasse 1, D-91058 Erlangen, Germany

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo702573z

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4. Over One Hundred Peptide-Activated G Protein-Coupled Receptors Recognize Ligands with Turn Structure

5. Enantiopure 4- and 5-Aminopiperidin-2-ones: Regiocontrolled Synthesis and Conformational Characterization as Bioactive β-Turn Mimetics

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