Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Adam W. Franz"'
Publikováno v:
Molecules, Vol 26, Iss 10, p 2950 (2021)
The Cu-catalyzed alkyne-azide 1,3-dipolar cycloaddition variant provides a highly efficient entry to conjugated triazolyl-substituted (oligo)phenothiazine organosilicon derivatives with luminescence and reversible redox characteristics. Furthermore,
Externí odkaz:
https://doaj.org/article/4750f9ede3a444fe9e4307b5ebf4e0b6
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 6, Iss 1, p 72 (2010)
(Oligo)phenothiazinyl thioacetates, synthesized by a one-pot sequence, are electrochemically oxidizable and highly fluorescent. SAMs can be readily formed from thiols prepared by in situ deprotection of the thioacetates in the presence of a gold-coat
Externí odkaz:
https://doaj.org/article/9d994c94235444ff87f85311af4bbad1
Publikováno v:
Nachrichten aus der Chemie. 70:44-47
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::91b54c3ddff5b8bf1f3791b1db5e6a6a
https://doi.org/10.1002/nadc.20224129344
https://doi.org/10.1002/nadc.20224129344
Autor:
Adam W. Franz, Helmut Kronemayer, Daniel Pfeiffer, Roman D. Pilz, Gänther Reuss, Walter Disteldorf, Armin Otto Gamer, Albrecht Hilt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8fd0e5685c9128a7287081a2323f2b1b
https://doi.org/10.1002/14356007.a11_619.pub2
https://doi.org/10.1002/14356007.a11_619.pub2
Publikováno v:
Letters in Organic Chemistry. 9:211-217
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9864a153d098e71a90620c1bcb12ab1d
https://doi.org/10.2174/157017812800167529
https://doi.org/10.2174/157017812800167529
Publikováno v:
Journal of the American Chemical Society. 133:4766-4769
An atom-economical method for the direct synthesis of [3.1.0]- and [4.1.0]-bicyclic frameworks via Ru-catalyzed redox bicycloisomerization of enynols is reported. The presented results highlight the unique reactivity profile of propargyl alcohols, wh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3e47685b35dd6c29487e67aae718d86
https://doi.org/10.1021/ja200971v
https://doi.org/10.1021/ja200971v
Autor:
Thomas Müller, Uli Lemmer, Adam W. Franz, David Müller, Alexander Colsmann, Christa S. Barkschat, Klaus Meerholz, Markus Sailer
Publikováno v:
Macromolecular Symposia. 287:1-7
Monodisperse oligophenothiazines are rapidly synthesized in good yields by use of Suzuki arylation. These well defined oligomers reveal both highly fluorescence and low oxidation potentials. As a consequence of intense electronic coupling as supporte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3f792c1870aee09e939fe5efd3450de8
https://doi.org/10.1002/masy.201050101
https://doi.org/10.1002/masy.201050101
Autor:
Biprajit Sarkar, Thomas Müller, Martin Hartmann, Zhou Zhou, Adam W. Franz, Raluca Turdean, Alex Wagener, Werner R. Thiel, Stefan Ernst
Publikováno v:
European Journal of Organic Chemistry. 2009:3895-3905
Mesoporous hybrid materials of (oligo)phenothiazines covalently grafted onto MCM-41 or SBA-15 silica have been readily prepared from (oligo)phenothiazinyl carbamates. The phenothiazine precursors show interesting electronic properties according to el
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f864958872681ad3f3686512eb3763fa
https://doi.org/10.1002/ejoc.200900332
https://doi.org/10.1002/ejoc.200900332
Publikováno v:
Tetrahedron Letters. 49:3300-3303
(Oligo)phenothiazinyl nitriles were synthesized in good to very good yields from bromo (oligo)phenothiazines via the Beller cyanation protocol either under conductive or under dielectric heating using NMP as a solvent. Their electronic properties wer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2a8f2b205f9d87d7521465909d92b3a8
https://doi.org/10.1016/j.tetlet.2008.03.071
https://doi.org/10.1016/j.tetlet.2008.03.071
Publikováno v:
The Journal of Organic Chemistry. 73:1795-1802
Phenothiazine is coupled under Buchwald-Hartwig conditions with bromo anthracenes and perylene as substrates to give phenothiazine-anthracene and phenothiazine-perylene dyads and triads. Investigation of the electronic properties of these sterically
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe9429539405a6cd9f966c1b70c71963
https://doi.org/10.1021/jo702389v
https://doi.org/10.1021/jo702389v