Ring-Closing Metathesis Approaches for the Solid-Phase Synthesis of Cyclic Peptoids-Reference-Cited by-同舟云学术

Ring-Closing Metathesis Approaches for the Solid-Phase Synthesis of Cyclic Peptoids

Published:2011-03-08 Issue:7 Volume:13 Page:1582-1585
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Khan Sharaf Nawaz¹,Kim Arim¹,Grubbs Robert H.¹,Kwon Yong-Uk¹

Affiliation:

1. Department of Chemistry and Nano Science, Ewha Womans University, Seoul 120-750, South Korea, and The Arnold and Mabel Beckman Laboratory of Chemical Synthesis, Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, California 91125, United States

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol200226z

Reference36 articles.

1. Converting a Peptide into a Drug: Strategies to Improve Stability and Bioavailability

2. Mimicry of bioactive peptides via non-natural, sequence-specific peptidomimetic oligomers

3. Efficient method for the preparation of peptoids [oligo(N-substituted glycines)] by submonomer solid-phase synthesis

4. Microwave-Assisted Solid-Phase Synthesis of Peptoids

5. Comparison of the proteolytic susceptibilities of homologous L-amino acid, D-amino acid, and N-substituted glycine peptide and peptoid oligomers

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