Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Charlotte F. Gers-Panther"'
Autor:
Charlotte F. Gers-Panther, Walter Frank, Katrin Hoffmann, Ute Resch-Genger, Nithiya Nirmalananthan, Thomas Müller, Daniel Kage, Thomas Behnke
Publikováno v:
The Journal of Physical Chemistry C. 122:11119-11127
Aggregation-induced emission (AIE) has been meanwhile observed for many dye classes and particularly for fluorophores containing propeller-like groups. Herein, we report on the AIE characteristics of a series of four hydrophobic pyrrolidinylvinylquin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e57318202f1b856f997f08d3e1f3f880
https://doi.org/10.1021/acs.jpcc.8b01425
https://doi.org/10.1021/acs.jpcc.8b01425
Publikováno v:
Chemistry - A European Journal. 22:2020-2031
A convergent and diversity-oriented approach to the unusual furo[2,3-c]isoquinoline scaffold is presented. This serendipity-driven approach is characterized by an Ugi multicomponent reaction, which gives the substrate for a palladium-catalyzed insert
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce512473ed5bf03fb758c4fb32ecbcf5
https://doi.org/10.1002/chem.201504335
https://doi.org/10.1002/chem.201504335
Autor:
Charlotte F. Gers-Panther, Thomas Müller, Mirko Matthias Lindic, Matthias Zajonz, Michael Schmitt
Publikováno v:
Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy. 228:117574
The excited state dipole moment of 2-[(4-methoxyphenyl)ethynyl]-3-(1-methyl-1H-indol-3-yl)-quinoxaline has been determined in ethyl acetate solution using the method of thermochromic shifts. Three different models have been tested and are compared to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cef6df3f549fcae05693f215a63ec54b
https://doi.org/10.1016/j.saa.2019.117574
https://doi.org/10.1016/j.saa.2019.117574
Autor:
Irina Gruber, Christoph Janiak, Simon P. Höwedes, Charlotte F. Gers-Panther, Thomas Müller, Franziska K. Merkt
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 24(32)
2-Substituted 3-ethynylquinoxaline chromophores can be readily synthesized by a consecutive activation-alkynylation-cyclocondensation (AACC) one-pot sequence in a three-component manner. In comparison with the previously published four-component glyo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7fb3c2d2dc03fcd2c8d91bb51c41d77
https://pubmed.ncbi.nlm.nih.gov/29425410
https://pubmed.ncbi.nlm.nih.gov/29425410
Autor:
Christian Würth, Ute Resch-Genger, Charlotte F. Gers-Panther, Walter Frank, Jan Nordmann, Theresa Seiler, Thomas Behnke, Henry Fischer, Thomas Müller
Publikováno v:
The Journal of organic chemistry. 82(1)
3-Aminovinylquinoxalines are readily accessible from (hetero)aryl glyoxylic acids or heterocyclic π-nucleophiles by consecutive four- and five-component syntheses in the sense of an activation-alkynylation-cyclocondensation-addition sequence or glyo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2a28479a2cd86d799d3e01777ae591b
https://pubmed.ncbi.nlm.nih.gov/27976907
https://pubmed.ncbi.nlm.nih.gov/27976907
Publikováno v:
ChemInform. 47
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d6de615ad90bc53ca06d85fd4a58c60e
https://doi.org/10.1002/chin.201627181
https://doi.org/10.1002/chin.201627181
Propynones and 3-butyne-1,2-diones are densely substituted bi- and trifunctional electrophiles that can be generated by Pd-Cu- or by Cu-catalyzed alkynylation. The mild and general reaction conditions allow a straightforward entry to consecutive mult
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6b5f0b67b4a188a9fc7575bb7f63d921
https://doi.org/10.1016/bs.aihch.2016.04.007
https://doi.org/10.1016/bs.aihch.2016.04.007
Autor:
Christoph Janiak, Franziska K. Merkt, Irina Gruber, Simon P. Höwedes, Charlotte F. Gers-Panther, Thomas Müller
Publikováno v:
Chemistry - A European Journal. 24:8017-8017
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::082661217f2aeca62c83fc131abad369
https://doi.org/10.1002/chem.201802060
https://doi.org/10.1002/chem.201802060