Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Michael C. D. Fürst"'
Autor:
Lisa-Marie Altmann, Gerald Pratsch, Markus R. Heinrich, Michael C. D. Fürst, Eva Gans, Viviane Zantop
Publikováno v:
Organic letters. 22(2)
Aryl radicals generated in the aqueous phase of biphasic mixtures have—regardless of a comparably low polarity— a strong preference to react with aromatic substrates in the aqueous phase and not to undergo phase-transfer into a lipophilic phase,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::792ee02198a4fc621abf9b4ee1dac76b
https://pubmed.ncbi.nlm.nih.gov/31904970
https://pubmed.ncbi.nlm.nih.gov/31904970
Publikováno v:
Tetrahedron. 74:5289-5294
Frozen aryldiazonium chlorides have been investigated in radical alkene and arene functionalizations. Through freezing at – 84 °C, aryldiazonium chlorides, which otherwise show significant decomposition in aqueous solution after several hours at r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5bda2de2c034895081f746b118705d31
https://doi.org/10.1016/j.tet.2018.05.089
https://doi.org/10.1016/j.tet.2018.05.089
Autor:
Christiane Östreicher, Gerald Pratsch, Stefanie K. Fehler, Michael C. D. Fürst, Markus R. Heinrich, Monika Pischetsrieder
Publikováno v:
Tetrahedron. 72:7888-7893
The radical arylation of the phenolic side chain of tyrosine in peptides was investigated. Aryl radicals were generated from aryldiazonium salts using titanium(III) chloride as stoichiometric reductant. Due to the high selectivity with which 3-arylty
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::547c969d5ce286e673e59b602aefb24d
https://doi.org/10.1016/j.tet.2016.04.084
https://doi.org/10.1016/j.tet.2016.04.084
Publikováno v:
The Journal of Organic Chemistry. 81:5752-5758
The titanium(III)-mediated radical arylation of 3-hydroxypyridines was found to proceed with high regioselectivity for the 2-position. Using aryldiazonium chlorides, which were prepared from the corresponding anilines, as aryl radical sources, a rang
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2bac2ad6ba2e52599395a4912bcaccf
https://doi.org/10.1021/acs.joc.6b00894
https://doi.org/10.1021/acs.joc.6b00894
Publikováno v:
European Journal of Organic Chemistry. 2016:3051-3055
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e4d41d901b6896248386a03fa84e361e
https://doi.org/10.1002/ejoc.201600377
https://doi.org/10.1002/ejoc.201600377
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 23(61)
In the absence of a photocatalyst and other additives, the radical arylation of diverse arenes and heteroarenes has been achieved with aryldiazonium salts under visible-light irradiation from a blue light-emitting diode (LED). Although the course of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34932f55bd5f88f51becf8933c5ecf32
https://pubmed.ncbi.nlm.nih.gov/28836697
https://pubmed.ncbi.nlm.nih.gov/28836697
Autor:
Roland Schüle, Ludovica Morera, Johanna Senger, Manfred Jung, Henriette Franz, Michael C. D. Fürst, Martin Roatsch, Mirjam Hau, Inga Hoffmann, Markus R. Heinrich
Publikováno v:
ChemMedChem. 11(18)
Overexpression of the histone lysine demethylase KDM4A, which regulates H3K9 and H3K36 methylation states, has been related to the pathology of several human cancers. We found that a previously reported hydroxamate-based histone deacetylase (HDAC) in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa6895f61d45876cebeab0e5f30fa1b4
https://pubmed.ncbi.nlm.nih.gov/27505861
https://pubmed.ncbi.nlm.nih.gov/27505861