Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Yuki Ishido"'
Publikováno v:
ACS macro letters. 8(6)
A methodology for producing dual structural systems of macromolecules, which involves flipping the unsymmetrical aromatic rings on the main chain is presented. Previously, we reported a non-natural polypeptide containing an aromatic ring on the pepti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78eda29c2d6a197f8a16913e56920308
https://pubmed.ncbi.nlm.nih.gov/35619526
https://pubmed.ncbi.nlm.nih.gov/35619526
Publikováno v:
Polymer Chemistry. 11:6241-6250
Asymmetric polymerization is a promising method for constructing sophisticated backbones that contain asymmetric carbons on the main chain. Herein, we report the precise design and synthesis of a novel polymer backbone that induces a helical structur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::811b3922a53eb97b1b4eca7afc3e1c8d
https://doi.org/10.1039/d0py01073a
https://doi.org/10.1039/d0py01073a
Autor:
Kiyotaka Onitsuka, Naoka Fujii, Naoya Kanbayashi, Takeharu Haino, Taka-aki Okamura, Yuki Ishido
Publikováno v:
Chemical communications (Cambridge, England). 56(18)
We synthesized “glyco-arylopeptides”, whose folding structure significantly changes depending on the kind of saccharide in their side chain. The saccharide moiety interacts with the main chain via hydrogen bonding, and the non-natural polypeptide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::89fcd7d605320c60301b97014a91b43a
https://pubmed.ncbi.nlm.nih.gov/32022009
https://pubmed.ncbi.nlm.nih.gov/32022009
Publikováno v:
Macromolecules. 50:5301-5307
Herein, we present a novel synthetic strategy, to amino-acid-free peptide synthesis based on postpolymerization conversion, for chiral nonnatural polypeptides. Optically active poly-N-alkoxyamides were prepared by our asymmetric polymerization as pre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::77d7ac148eeac27215b6fe5da4ee5b21
https://doi.org/10.1021/acs.macromol.7b01426
https://doi.org/10.1021/acs.macromol.7b01426
Publikováno v:
Polym. Chem.. 8:985-994
In this study, we examined novel synthetic methods for optically active polymers bearing various side chains from post-polymerization modification of a single optically active polymer. The side chain in the optically active polymer (poly-1) which was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d2946febc80558f02748f85cde9d344d
https://doi.org/10.1039/c6py01946c
https://doi.org/10.1039/c6py01946c
Publikováno v:
Macromolecular Rapid Communications. 42:2100250
Controlling the structural transition between well-defined architectures found in living system is essential in polymer chemistry as well as material science. Herein, the reversible conformational switch of a non-natural polypeptide with an aromatic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da626ef4b30049d7349adee0d1c0c72f
https://doi.org/10.1002/marc.202100250
https://doi.org/10.1002/marc.202100250
Publikováno v:
Macromolecules; Jul2017, Vol. 50 Issue 14, p5301-5307, 7p