(+)- and (−)-2-Aminocyclobutane-1-carboxylic Acids and Their Incorporation into Highly Rigid β-Peptides: Stereoselective Synthesis and a Structural Study-Reference-Cited by-同舟云学术

(+)- and (−)-2-Aminocyclobutane-1-carboxylic Acids and Their Incorporation into Highly Rigid β-Peptides: Stereoselective Synthesis and a Structural Study

Published:2005-09-01 Issue:20 Volume:70 Page:7963-7971
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Izquierdo Sandra¹,Rúa Federico¹,Sbai Abdelouahid¹,Parella Teodor¹,Álvarez-Larena Ángel¹,Branchadell Vicenç¹,Ortuño Rosa M.¹

Affiliation:

1. Departament de Química, Servei de RMN, and Unitat de Cristal·lografia, Universitat Autònoma de Barcelona, 08193 Bellaterra, Barcelona, Spain

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo0510843

Reference37 articles.

1. 2,4-Methanoproline (2-carboxy-2,4-methanopyrrolidine) and 2,4-methanoglutamic acid (1-amino-1,3-dicarboxycyclobutane) in seeds of Ateleia herbert smithii Pittier (Leguminosae)

2. The World ofβ- andγ-Peptides Comprised of Homologated Proteinogenic Amino Acids and Other Components

3. Stereospecific synthesis of (1S,2S)-1-hydroxy-2-[(S)-valylamino]-cyclobutane-1-acetic acid, a novel microbial antimetabolite

4. The synthesis and antimicrobial activity of (1,2)-1-hydroxy-2-[(s)-valylamino]cyclobutane-1-acetic acid (1) and (1, 2)-1-hydroxy-2-aminocyclobutane-1-acetic acid (2)

5. 1-Aminocyclobutanecarboxylic Acid Derivatives as Novel Structural Elements in Bioactive Peptides: Application to Tuftsin Analogs

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