Steric Effects on the Amide Isomer Equilibrium of Prolyl Peptides. Synthesis and Conformational Analysis of N-Acetyl-5-tert-butylproline N‘-Methylamides-Reference-Cited by-同舟云学术

Steric Effects on the Amide Isomer Equilibrium of Prolyl Peptides. Synthesis and Conformational Analysis of N-Acetyl-5-tert-butylproline N‘-Methylamides

Published:1996-01-01 Issue:51 Volume:118 Page:12902-12908
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Beausoleil Eric¹,Lubell William D.¹

Affiliation:

1. Contribution from the Département de chimie, Université de Montréal, C. P. 6128, Succursale Centre Ville, Montréal, Québec, Canada H3C 3J7

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja962013b

Reference42 articles.

1. Cis/trans conformational equilibrium across the cysteine6-proline peptide bond of oxytocin, arginine vasopressin, and lysine vasopressin

2. Approaches to peptidomimetics which serve as surrogates for the cis amide bond: novel disulfide-constrained bicyclic hexapeptide analogs of somatostatic.

3. The synthesis and conformational analysis of a pair of diastereomeric, conformationally constrained peptides with opposite amide bond geometries

4. The synthesis and conformational analysis of a pair of diastereoisomeric cyclic peptides with cis and transamide bonds, respectively

5. The conformation of cyclo-[(R)-cysteinyl-(R)-cysteine] in solution

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