Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Markus Sailer"'
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
Publikováno v:
Synlett. 2008:845-848
Double bromine-lithium exchange and sequential trapping of the dilithio intermediate with different electrophiles gives rise to the formation of unsymmetrically substituted (hetero)arenes in a one-pot fashion.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d5e9a2836d2735a4d4b642c462d1a209
https://doi.org/10.1055/s-2008-1042911
https://doi.org/10.1055/s-2008-1042911
Publikováno v:
Journal of Organometallic Chemistry. 691:299-308
Oligomeric ferrocene–phenothiazine systems, a novel class of organometallic–organic hybrid electrophores, are easily accessible by Suzuki coupling of iodo ferrocenes and phenothiazinyl and diphenothiazinyl pinacolyl boronates. The triad and the p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1cc3f1d9c428454b47b20b7f5edb1aef
https://doi.org/10.1016/j.jorganchem.2005.08.012
https://doi.org/10.1016/j.jorganchem.2005.08.012
Publikováno v:
European Journal of Organic Chemistry. 2006:423-435
3-Acceptor-substituted and 3,7-bisacceptor-substituted phenothiazines can be synthesized in moderate to excellent yields through Suzuki cross-coupling reactions between phenothiazin-3-yl pinacolyl boronates or phenothiazin-3,7-diyl bis(pinacolyl boro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b882f4c363982b224b6b0e8cdac2c727
https://doi.org/10.1002/ejoc.200500539
https://doi.org/10.1002/ejoc.200500539
Publikováno v:
ChemInform. 33
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7adedff81270b01aceff24faef6388c9
https://doi.org/10.1002/chin.200241157
https://doi.org/10.1002/chin.200241157
Publikováno v:
ChemInform. 39
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d1e45d4e765570705a535ed611d25e01
https://doi.org/10.1002/chin.200831030
https://doi.org/10.1002/chin.200831030
Publikováno v:
The Journal of organic chemistry. 68(19)
Bromine−lithium exchange of the mono- and dibromophenothiazines 1 and 3a regiospecifically furnishes upon electrophilic trapping with iodine the iodo- and diiodophenothiazines 2, 3b, and 3d in excellent yield. The 3-bromo-7-iodophenothiazine 3d can
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ea5e0843a1e2fe0715d4241c8fd5b94
https://pubmed.ncbi.nlm.nih.gov/12968908
https://pubmed.ncbi.nlm.nih.gov/12968908
Publikováno v:
Synthesis. 2002
Phenothiazinylboronic acid derivatives 3,7 and 9, useful building blocks for the construction of oligophenothiazines, are readily synthesized in good yield from brominated phenothiazines 5 and 6 by bromine-lithium exchange followed by trapping with t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::25c713c850dac4af535af1b7cca06d8f
https://doi.org/10.1055/s-2002-32527
https://doi.org/10.1055/s-2002-32527