Spiro β-Lactams as β-Turn Mimetics. Design, Synthesis, and NMR Conformational Analysis-Reference-Cited by-同舟云学术

Spiro β-Lactams as β-Turn Mimetics. Design, Synthesis, and NMR Conformational Analysis

Published:2001-08-24 Issue:19 Volume:66 Page:6333-6338
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Alonso Eduardo¹,López-Ortiz Fernando¹,del Pozo Carlos¹,Peralta Emma¹,Macías Alberto¹,González Javier¹

Affiliation:

1. Departamento de Química Orgánica e Inorgánica Universidad de Oviedo, 33071 Oviedo, Spain, Área de Química Orgánica, Universidad de Almería Carretera de Sacramento s/n 04120 Almería, Spain, and Química ID Asturias, SL c/Cat. Adolfo A. Buylla, 26, 33013 Oviedo, Spain

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo015714m

Reference21 articles.

1. Peptidomimetics—Tailored Enzyme Inhibitors

2. Design, Synthesis, and Dopamine Receptor Modulating Activity of Spiro Bicyclic Peptidomimetics of l-Prolyl-l-leucyl-glycinamide

3. Asymmetric Catalysis with Libraries of Palladium β-Turn Phosphine Complexes

4. Asymmetric Conjugate Addition of Azide toα,β-Unsaturated Carbonyl Compounds Catalyzed by Simple Peptides

5. Kinetic Resolution of Alcohols Catalyzed by Tripeptides Containing the N-Alkylimidazole Substructure

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