Novel Consecutive β- and γ-Turn Mimetics Composed of α-Aminooxy Tripeptides-Reference-Cited by-同舟云学术

Novel Consecutive β- and γ-Turn Mimetics Composed of α-Aminooxy Tripeptides

Published:2003-02-27 Issue:7 Volume:5 Page:971-974
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Baek Bong-hyeon¹,Lee Myung-ryul¹,Kim Kwang-Yon¹,Cho Ung-In¹,Boo Doo Wan¹,Shin Injae¹

Affiliation:

1. Department of Chemistry, Yonsei University, Seoul 120-749, Korea

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol020233q

Reference13 articles.

1. (b) Creighton, T. E.Proteins: Structures and MolecularProperties; Freeman: New York, 1993.

2. Reverse Turns in Peptides and Protein

3. Rose, G. D.; Gierasch, L. M.; Smith, J. A. InTurns in Peptides and Proteins; Anfinsen, C. B., Edsall, J. T., Richards, F. M., Eds.; Academic Press: Orlando, FL, 1985; Vol. 37, pp 1−109.

4. 1H-nmr studies of receptor-selective substance P analogues reveal distinct predominant conformations in DMSO-d6

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