Zobrazeno 1 - 10
of 63
pro vyhledávání: '"Frédéric, Coutrot"'
Publikováno v:
ChemistryOpen, Vol 13, Iss 10, Pp n/a-n/a (2024)
Abstract [cn]daisy chain molecular muscle architectures are self‐assemblies of hermaphrodite monomers, which usually contain a macrocycle unit linked to a molecular thread that contains sites of interactions – i. e. molecular stations – for the
Externí odkaz:
https://doaj.org/article/84e0168185684944a79f5a5b9b121042
Autor:
Frédéric Coutrot, Maxime Gauthier
Publikováno v:
Chemistry – A European Journal. 27:17576-17580
This paper reports the synthesis and study of new pH-sensitive DB24C8-based [2]rotaxane molecular shuttles that contain within their axle the following four potential sites of interaction for the DB24C8: ammonium, amine, Weinreb amide and ketone. At
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe54aebf05c6e7eecfad0f15d2da9064
https://doi.org/10.1002/chem.202103805
https://doi.org/10.1002/chem.202103805
Autor:
Victor Koehler, Maxime Gauthier, Chenhao Yao, Karine Fournel-Marotte, Philip Waelès, Brice Kauffmann, Ivan Huc, Frédéric Coutrot, Yann Ferrand
Publikováno v:
Chemical Communications
Chemical Communications, 2022, 58 (62), pp.8618-8621. ⟨10.1039/D2CC03066G⟩
Chemical Communications, 2022, 58 (62), pp.8618-8621. ⟨10.1039/D2CC03066G⟩
The wrapping of an aromatic oligoamide helix around an active ester-containing [2]rotaxane enforced the sliding and the sequestration of the surrounding macrocycle around a part of the axle for which it has no formal affinity. The foldamer-mediated c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff89d5d92ca83040e396732134e836d9
https://pubmed.ncbi.nlm.nih.gov/35786713
https://pubmed.ncbi.nlm.nih.gov/35786713
Autor:
Ivan Huc, Yann Ferrand, Maxime Gauthier, Frédéric Coutrot, Caroline Clavel, Brice Kauffmann, Victor Koehler
Publikováno v:
Angewandte Chemie International Edition
Angewandte Chemie International Edition, Wiley-VCH Verlag, 2021, 60 (15), pp.8380-8384. ⟨10.1002/anie.202100349⟩
Angewandte Chemie International Edition, Wiley-VCH Verlag, 2021, 60 (15), pp.8380-8384. ⟨10.1002/anie.202100349⟩
The design and synthesis of a novel rotaxane/foldaxane hybrid architecture is reported. The winding of an aromatic oligoamide helix host around a dumbbell-shaped thread-like guest, or axle, already surrounded by a macrocycle was evidenced by NMR spec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c5d61e7a1561f88c9be218e05b0b235
https://doi.org/10.1002/ange.202100349
https://doi.org/10.1002/ange.202100349
Publikováno v:
European Journal of Organic Chemistry. 2022
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6abbb13f6a3254a2b84d1bfa669b3130
https://doi.org/10.1002/ejoc.202101385
https://doi.org/10.1002/ejoc.202101385
Publikováno v:
Molecules, Vol 18, Iss 9, Pp 11553-11575 (2013)
The synthesis of a peptide-containing lasso molecular switch by a self-entanglement strategy is described. The interlocked [1] rotaxane molecular machine consists of a benzometaphenylene[25]crown-8 (BMP25C8) macrocycle surrounding a molecular axle. T
Externí odkaz:
https://doaj.org/article/bef745649fc644538d3ca2a4d8ef264b
Publikováno v:
ChemPlusChem. 87
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2a6398a90de8df58bc901393203b0765
https://doi.org/10.1002/cplu.202200018
https://doi.org/10.1002/cplu.202200018
Publikováno v:
ChemPlusChem. 87(3)
Although not often encountered, cyclic interlocked molecules are appealing molecular targets because of their restrained tridimensional structure which is related to both the cyclic and interlocked shapes. Interlocked molecules such as rotaxane build
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1bf4267c4bf018d883f57438af00b315
https://pubmed.ncbi.nlm.nih.gov/34811956
https://pubmed.ncbi.nlm.nih.gov/34811956
Autor:
Frédéric Coutrot, Maxime Gauthier
Publikováno v:
European Journal of Organic Chemistry. 2022
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b17ae25514a3e9a00ce56f1892783991
https://doi.org/10.1002/ejoc.202101201
https://doi.org/10.1002/ejoc.202101201
Autor:
Frédéric Coutrot, Maxime Gauthier
Publikováno v:
European Journal of Organic Chemistry. 2019:3391-3395
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f90c9c3fdd6f0f675d97658b4d348e70
https://doi.org/10.1002/ejoc.201900046
https://doi.org/10.1002/ejoc.201900046