Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Kristin Klaue"'
Publikováno v:
Cell Reports Methods. :100486
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::35429b08f69827c371a0b4f8f1e38b06
https://doi.org/10.1016/j.crmeth.2023.100486
https://doi.org/10.1016/j.crmeth.2023.100486
Publikováno v:
Journal of the American Chemical Society. 142:11857-11864
The use of low-intensity NIR light to operate molecular switches offers several potential advantages including enhanced penetration into bulk materials, in particular biological tissues, and reduced radiation damage due to the limited photon energies
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2e659859b00bfe0c09940cc41f79923
https://doi.org/10.1021/jacs.0c04219
https://doi.org/10.1021/jacs.0c04219
Publikováno v:
Broløs, L, Klaue, K, Bendix, J, Grubert, L, Hecht, S & Nielsen, M B 2021, ' Stabilizing Indigo Z-isomer via Intramolecular Associations of Redox-Active Appendages ', European Journal of Organic Chemistry, vol. 2021, no. 46, pp. 6304-6311 . https://doi.org/10.1002/ejoc.202100781
Photoswitchable small molecules, such as N , N'- disubstituted indigos, have received great interest within fields such as pharmacology, energy storage, and functional materials, as they represent key building blocks for reversible and non-invasive c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee448c02d96c7761d378de994642ca37
https://curis.ku.dk/ws/files/279650658/Stabilizing_Indigo_Z_isomer_via_Intramolecular_Associations_of_Redox_Active_Appendages_accepted_version_.pdf
https://curis.ku.dk/ws/files/279650658/Stabilizing_Indigo_Z_isomer_via_Intramolecular_Associations_of_Redox_Active_Appendages_accepted_version_.pdf
Publikováno v:
Angewandte Chemie International Edition. 57:1414-1417
The success of photopharmacology is inevitably tied to the availability of photoswitches, which can be operated within the biological window (λ=650-1450 nm) to maximize penetration in tissue. A general design strategy has been devised and a dihydrop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::726aae6530f53204539a42877072ddcf
https://doi.org/10.1002/anie.201709554
https://doi.org/10.1002/anie.201709554
Publikováno v:
Angewandte Chemie. 130:1429-1432
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::024a7b158895903f8e4c14c45c2dcb63
https://doi.org/10.1002/ange.201709554
https://doi.org/10.1002/ange.201709554
Publikováno v:
ChemPlusChem. 82:1025-1029
Although aromaticity is a key concept in chemistry that is frequently used to explain the structure and reactivity of organic compounds, it remains challenging to actually measure this property. Proper probes allow for an experimental quantification
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::794464d147be5045ee82d2a3a3317aa1
https://doi.org/10.1002/cplu.201700068
https://doi.org/10.1002/cplu.201700068
Publikováno v:
European Journal of Organic Chemistry. 2016:5309-5320
A highly stereoselective de-Bruyn–Ekenstein rearrangement/aldol condensation/intramolecular oxa-Michael cascade reaction of unprotected ketoses with ketones was elaborated. By the utilization of this new and operationally simple methodology an acce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::68032ddc45fcb137f0eb009db1f36a6a
https://doi.org/10.1002/ejoc.201601058
https://doi.org/10.1002/ejoc.201601058