About: Interconversion of single and double helices formed from synthetic molecular strands

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scientific article published in Nature

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rdf:type	Item
description	artículu científicu (ast) wetenschappelijk artikel (nl) article publié dans la revue scientifique Nature (fr) im Oktober 2000 veröffentlichter wissenschaftlicher Artikel (de) scientific article published in Nature (en) наукова стаття, опублікована в Nature в жовтні 2000 (uk)
publication date	wds:Q59054475-86540F68-EF92-48C5-AEA4-AB88E9F4553B
publication date	2000-10-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q59054475-44CBC710-CEB2-4D92-8078-E1C519BCE1A8
language of work or name	English
exact match	wds:Q59054475-DB432E4D-29E7-4C72-8D4C-CC71C2C37EB9
exact match	https://scigraph.springernature.com/pub.10.1038/35037545
cites work	wds:Q59054475-24EA0DEB-177F-4BEA-BCF2-21C7AF674C1C wds:Q59054475-41574ABE-C04F-4A2D-928C-4B91B1125C06 wds:Q59054475-5BA2EFED-2061-4187-A0E6-2702961E31A8 wds:Q59054475-6850E5D9-1E91-4BDB-8F83-588F45FD44B2 wds:Q59054475-6A409030-0C0A-463D-A323-08E9EFB1BC4F wds:Q59054475-815EE009-D929-45B0-83C1-FB7B7A57AE69 wds:Q59054475-8232A3A6-E224-428F-BBE0-8FA7AFBF0B45 wds:Q59054475-8B48451D-7830-4650-8CB6-8B906654ECE9 wds:Q59054475-CF480C53-0F57-4E80-8C50-CF8CDACEC2DD wds:Q59054475-F2560DEE-4EEC-47D3-B559-7F0905E30D2B wds:Q59054475-F30DE4D7-69E7-4C23-807C-606EE112BFD6 wds:Q59054475-FDCBB268-D19F-4353-9699-FF259164CD42
cites work	Solvophobically driven folding of nonbiological oligomers Template-induced and molecular recognition directed hierarchical generation of supramolecular assemblies from molecular strands The aggregation of gramicidin A in solution. Self-Assembly of a Circular Double Helicate Self-Assembly of Disk-Shaped Molecules to Coiled-Coil Aggregates with Tunable Helicity Three-dimensional structure at 0.86 A of the uncomplexed form of the transmembrane ion channel peptide gramicidin A Encoded Helical Self-Organization and Self-Assembly into Helical Fibers of an Oligoheterocyclic Pyridine - Pyridazine Molecular Strand Self-assembly of a double-helical complex of sodium DNH deoxyribonucleohelicates: self assembly of oligonucleosidic double-helical metal complexes Ruthenium Complexes of a Simple Tridentate Ligand Bearing Two "Distal" Pyridine Bases The double pi pi 5.6 helix of gramicidin A predominates in unsaturated lipid membranes Regularly alternating L,D-peptides. II. The double-stranded right-handed antiparallel beta-helix in the structure of t-Boc-(L-Phe-D-Phe)4-OMe
author name string	wds:Q59054475-0BC9F15D-0905-458D-9549-575C059541BB wds:Q59054475-64D8DB1D-BB0B-40AD-A70E-7EF2B4C3CA1E wds:Q59054475-730FAA90-172C-48F6-84E5-1A5EB88EBB6C wds:Q59054475-D8C9C241-1578-4A11-B69E-F4BE3999AF21 wds:Q59054475-E0DA0D02-F15B-4CAD-B15B-72654BE9C746
author name string	Lehn JM Krische MJ Khoury RG Berl V Huc I
rdfs:label	Interconversion of single and double helices formed from synthetic molecular strands (en) Interconversion of single and double helices formed from synthetic molecular strands (nl)
skos:prefLabel	Interconversion of single and double helices formed from synthetic molecular strands (en) Interconversion of single and double helices formed from synthetic molecular strands (nl)
name	Interconversion of single and double helices formed from synthetic molecular strands (en) Interconversion of single and double helices formed from synthetic molecular strands (nl)
author	wds:Q59054475-24C330DC-E019-45AC-9CBE-22800536210F wds:Q59054475-7DBF6C27-7ADF-487D-BF0E-FFCFE7827E46
author	Jean-Marie Lehn Michael J. Krische
title	wds:Q59054475-D10FB0E3-C4A3-4C9C-BE9B-187F3F36A4D9
title	Interconversion of single and double helices formed from synthetic molecular strands (en)
page(s)	wds:Q59054475-D32DB53A-4A98-41A9-8E2A-F4151967C149
page(s)	720-723
instance of	wds:Q59054475-29305D0A-5494-489C-8809-6AF0EBE6FB4F
instance of	scholarly article
PubMed ID	wds:Q59054475-AEC0956B-0E96-4829-9643-5928A716738D
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/11048713
PubMed ID	11048713
published in	wds:Q59054475-B25212C0-E5EC-4871-B346-6B7B84D5DF72
published in	Nature
issue	wds:Q59054475-467DC3BD-8AC7-4CA8-99BC-A20AC40B259F
volume	wds:Q59054475-EB100F69-7C17-4F05-AE54-A0E8C958970A
issue	6805
volume	407
DOI	wds:Q59054475-CC2BBBF2-242C-4426-A069-A29F79EA47C4
DOI	http://dx.doi.org/10.1038/35037545
DOI	10.1038/35037545
Dimensions Publication ID	wds:Q59054475-3F1FC534-A59E-4929-B995-E775F5FC00DC
Dimensions Publication ID	1014361108
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q59054475
is cites work of	Foldamers as versatile frameworks for the design and evolution of function Benzoylurea oligomers: synthetic foldamers that mimic extended alpha helices. Cation-promoted hierarchical formation of supramolecular assemblies of self-organized helical molecular components Shape-persistent H-bonded macrocyclic aromatic pentamers POCl3-mediated H-bonding-directed one-pot synthesis of macrocyclic pentamers, strained hexamers and highly strained heptamers Artificial Molecular Machines Shape persistence delivers lock-and-key chloride binding in triazolophanes Something between the amazing functions and various morphologies of self-assembling peptides materials in the medical field Small-molecule-mediated G-quadruplex isolation from human cells Folding of Oligoviologens Induced by Radical–Radical Interactions Halide-guided oligo(aryl-triazole-amide)s foldamers: receptors for multiple halide ions Iterative design of a helically folded aromatic oligoamide sequence for the selective encapsulation of fructose. Folding-driven synthesis of oligomers Designing structural motifs for clickamers: exploiting the 1,2,3-triazole moiety to generate conformationally restricted molecular architectures. Mix and match backbones for the formation of H-bonded duplexes Cooperative duplex formation by synthetic H-bonding oligomers. New Modalities for Challenging Targets in Drug Discovery A self-assembled foldamer capsule: combining single and double helical segments in one aromatic amide sequence. Control over unfolding pathways by localizing photoisomerization events within heterosequence oligoazobenzene foldamers. Folding versus Self‐Assembling Chiral recognition in noncovalent bonding interactions between helicenes: right-handed helix favors right-handed helix over left-handed helix Metal-free double helices from abiotic backbones

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