Peptoid Oligomers with α-Chiral, Aromatic Side Chains: Sequence Requirements for the Formation of Stable Peptoid Helices-Reference-Cited by-同舟云学术

Peptoid Oligomers with α-Chiral, Aromatic Side Chains: Sequence Requirements for the Formation of Stable Peptoid Helices

Published:2001-06-20 Issue:28 Volume:123 Page:6778-6784
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Wu Cindy W.¹,Sanborn Tracy J.¹,Huang Kai¹,Zuckermann Ronald N.¹,Barron Annelise E.¹

Affiliation:

1. Contribution from the Department of Chemical Engineering, Northwestern University, Evanston, Illinois 60208, Structural Biology NMR Facility, Northwestern University, Evanston, Illinois 60208, and Chiron Technologies, Chiron Corporation, 4560 Horton Street, Emeryville, California 94608

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja003154n

Reference37 articles.

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

2. Reassignment of stereochemistry and total synthesis of the thrombin inhibitor cyclotheonamide B

3. Peptide Nucleic Acid. A Molecule with Two Identities

4. Solid-Phase Syntheses of Unnatural Biopolymers Containing Repeating Urea Units

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