Ortho-halogen effects: n→π* interactions, halogen bonding, and deciphering chiral attributes in N-aryl glycine peptoid foldamers
Author:
Funder
Department of Science and Technology
VGST
Publisher
Elsevier BV
Subject
Inorganic Chemistry,Organic Chemistry,Spectroscopy,Analytical Chemistry
Reference66 articles.
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3. Extraordinarily robust polyproline type I peptoid helices generated via the incorporation of α-chiral aromatic N -1-naphthylethyl side chains;Stringer;J. Am. Chem. Soc.,2011
4. N-naphthyl peptoid foldamers exhibiting atropisomerism;Paul;Org. Lett.,2012
5. The tert-butyl side chain: a powerful means to lock peptoid amide bonds in the cis conformation;Roy;Org. Lett.,2013
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1. DFT Studies on the Molecular Structure, Regioisomerism, Ground and Excited state Charge Transfer Properties of Spiro‐heterocycles;ChemistrySelect;2022-12-21
2. Deciphering C–H⋯O/X weak hydrogen bonding and halogen bonding interactions in aromatic peptoids;New Journal of Chemistry;2022
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