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Design, synthesis and conformational analysis of oligobenzanilides as multi-facial alpha-helix mimetics

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Title: Design, synthesis and conformational analysis of oligobenzanilides as multi-facial alpha-helix mimetics
Authors: Flack, T
Romain, C
White, A
Haycock, P
Barnard, A
Item Type: Journal Article
Abstract: The design, synthesis, and conformational analysis of an oligobenzanilide helix mimetic scaffold capable of simultaneous mimicry of two faces of an α-helix is reported. The synthetic methodology provides access to diverse monomer building blocks amenable to solid-phase assembly in just four synthetic steps. The conformational flexibility of model dimers was investigated using a combination of solid and solution state methodologies supplemented with DFT calculations. The lack of noncovalent constraints allows for significant conformational plasticity in the scaffold, thus permitting it to successfully mimic residues i, i+2, i+4, i+6, i +7, and i+9 of a canonical α-helix.
Issue Date: 21-Jun-2019
Date of Acceptance: 1-Jun-2019
URI: http://hdl.handle.net/10044/1/71702
DOI: https://dx.doi.org/10.1021/acs.orglett.9b01115
ISSN: 1523-7052
Publisher: American Chemical Society
Start Page: 4433
End Page: 4438
Journal / Book Title: Organic Letters
Volume: 21
Issue: 12
Copyright Statement: © 2019 American Chemical Society. This is an open access article published under a Creative Commons Attribution (CC-BY) License, which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited.
Sponsor/Funder: Wellcome Trust
Funder's Grant Number: 105603/Z/14/Z
Keywords: Science & Technology
Physical Sciences
Chemistry, Organic
Chemistry
PROTEIN-PROTEIN INTERACTIONS
EXPLORING KEY ORIENTATIONS
SMALL-MOLECULE INHIBITORS
ROTATION
INTERFACES
AMIDE
03 Chemical Sciences
Organic Chemistry
Publication Status: Published
Online Publication Date: 2019-06-12
Appears in Collections:Chemistry
Biological and Biophysical Chemistry