Targeting the protein backbone with aryl halides: systematic comparison of halogen bonding and π⋯π interactions using N-methylacetamide

M. O. Zimmermann; F. M. Boeckler

doi:10.1039/c5md00499c

by M. O. Zimmermann, Frank Boeckler

Published in MedChemComm by Royal Society of Chemistry (RSC).

2016 p500-505

Abstract

Systematic plane scans reveal a seamless transition from σ-hole interactions with the carbonyl oxygen to interactions with the amide π-electrons at increasing distances.
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Year 2016
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DOI 10.1039/c5md00499c

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Targeting the protein backbone with aryl halides: systematic comparison of halogen bonding and π⋯π interactions using N-methylacetamide release_vy6gbjuvf5ee7c4ijpjrsjlrmi

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