Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Felix Lederle"'
Publikováno v:
BMC Research Notes, Vol 12, Iss 1, Pp 1-6 (2019)
Abstract Objective A synthetic pathway to γ-hydroxy-α-(arylmethyl)carboxylic acids starting from α-angelica lactone and γ-butyrolactone was investigated. These γ-hydroxycarboxylic acids resemble structural motifs of lactic acid and amino acids.
Externí odkaz:
https://doaj.org/article/e49f316e844f45d184f35c4d2f3d4f21
Autor:
Philipp Memmel, Felix Lederle, Martin Söftje, Jannis Koch, Mingji Li, Wolfgang Schade, Eike G. Hübner
Publikováno v:
ACS Omega. 7:28408-28420
Long-flying sparks are an essential part of several pyrotechnic effects. Unfortunately, and in contrast to colored flames, the color space of sparks is basically limited to the black body curve. With low-boiling-point metals, vapor-phase combustion a
Autor:
Sebastian Mummel, Felix Lederle, Eike G. Hübner, Jan C. Namyslo, Martin Nieger, Andreas Schmidt
Publikováno v:
European Journal of Organic Chemistry. 26
Sydnone methides represent an almost unknown class of mesoionic compounds which possess exocyclic carbon substituents instead of oxygen (sydnones) or nitrogen (sydnone imines) in the 5-position of a 1,2,3-oxadiazolium ring. Unsubstituted 4-positions
Autor:
Sviatoslav Batsyts, Alexander Tombrink, Felix Lederle, Eike G. Hübner, Jan C. Namyslo, Martin Nieger, Andreas Schmidt
Publikováno v:
European Journal of Organic Chemistry. 2022
Dicationic bis-quinolinium salts possessing different types of conjugation are presented in which the hetareniums are separated by acetylenic or 1,4-diethynylbenzene spacers. Cross-conjugation is induced by interconnections via the 3-positions of the
Autor:
Eike G. Hübner, Andreas Schmidt, Felix Lederle, Martin Nieger, Sebastian Mummel, Jan C. Namyslo
Publikováno v:
Angewandte Chemie. 133:19032-19037
Wir beschreiben Sydnonmethide, von denen bisher nur ein einziges Beispiel in der Literatur erwähnt worden war. Sydnonmethide können zu Anionen deprotoniert werden, die als π-elektronenreiche anionische N-heterocyclische Carbene formulierbar sind.
Autor:
Jörg Adams, Felix Lederle, Sven Nagorny, Thea Weingartz, Wolfgang Maus-Friedrichs, Viktor Udachin, Andreas Schmidt, Eike G. Hübner, Sebastian Dahle
Publikováno v:
European Journal of Organic Chemistry. 2021:3178-3189
Syntheses of push–pull substituted non-symmetric bis(thienyl)ethenes (BTEs) possessing a central perfluorocyclopentene core are described. The substituent effects of anisole, phenole, and phenolate as well as pyridine, pyridinium, and N-methylpyrid
Autor:
Eike G. Hübner, Felix Lederle
Publikováno v:
Nachrichten aus der Chemie. 68:76-79
Publikováno v:
Zeitschrift für anorganische und allgemeine Chemie. 646:37-46
Commonly, sparks emit light according to the well-known black (gray) body radiation. Recently, we reported on color‐changing sparks based on erbium powder, which switch their light emission between black body emission (surface combustion) and eleme
Starting from 4-nitropyrazole, eight mesoionic pyrazolium-4-aminides were prepared by a six-step reaction sequence. The deprotonation of 1,2-disubstituted 4-amido-1H-pyrazolium salts by an anion exchange resin in its hydroxide form is the final step
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aaae39d4e33a88002f34c1bee1d2f982
https://publica.fraunhofer.de/handle/publica/429390
https://publica.fraunhofer.de/handle/publica/429390
Autor:
Jan C. Namyslo, Eike G. Hübner, Martin Nieger, Sebastian Mummel, Andreas Schmidt, Felix Lederle
Publikováno v:
Angewandte Chemie (International Ed. in English)
Sydnone methides are described from which only one single example has been mentioned in the literature so far. Their deprotonation gave anions which can be formulated as π‐electron rich anionic N‐heterocyclic carbenes. Sulfur and selenium adduct
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::006813da4f5708686ede05e928e2b4ab
https://dokumente.ub.tu-clausthal.de/receive/clausthal_mods_00002113
https://dokumente.ub.tu-clausthal.de/receive/clausthal_mods_00002113