Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Jonas F. Goebel"'
Publikováno v:
Angewandte Chemie International Edition.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::024d17974c4b5354187245e65293210f
https://doi.org/10.1002/anie.202301839
https://doi.org/10.1002/anie.202301839
Publikováno v:
Angewandte Chemie.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cfd1cf18eee756c5d96c1b45713708b6
https://doi.org/10.1002/ange.202301839
https://doi.org/10.1002/ange.202301839
Publikováno v:
Organic Letters. 24:3466-3470
In the presence of a [Ru(
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aeff30d0b4d19e45cfc4b938a8a5f72c
https://doi.org/10.1021/acs.orglett.2c01043
https://doi.org/10.1021/acs.orglett.2c01043
Autor:
Jonas F. Goebel, Julian Löffler, Zhongyi Zeng, Jens Handelmann, Albert Hermann, Ilja Rodstein, Tobias Gensch, Viktoria H. Gessner, Lukas J. Gooßen
Palladium-katalysierte Kupplungen von Silicium-Enolaten mit Arylelektrophilen sind von großem synthetischem Nutzen, aber oft auf teure Bromid-Substrate beschränkt. Eine vergleichende experimentelle Studie bestätigte, dass keines der etablierten Li
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46e8ed7f9b8144e11593bfa04e6fe37a
Autor:
Giulia Bertoli, Ángel Manu Martínez, Jonas F. Goebel, Debora Belmonte, Nardana Sivendran, Lukas J. Gooßen
Publikováno v:
Angewandte Chemie. 135
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::433cb63860953dfc61504f92e2f50020
https://doi.org/10.1002/ange.202215920
https://doi.org/10.1002/ange.202215920
Autor:
Jonas F. Goebel, Julian Löffler, Zhongyi Zeng, Jens Handelmann, Albert Hermann, Ilja Rodstein, Tobias Gensch, Viktoria H. Gessner, Lukas J. Gooßen
Publikováno v:
Angewandte Chemie (International ed. in English).
Palladium‐catalyzed couplings of silicon enolates with aryl electrophiles are of great synthetic utility, but often limited to expensive bromide substrates. A comparative experimental study confirmed that none of the established ligand systems allo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f54a73d3b51cfe09edac22bf5917d1b
https://pubmed.ncbi.nlm.nih.gov/36538000
https://pubmed.ncbi.nlm.nih.gov/36538000
Autor:
Yizhou Yang, Zoltan Takacs, Bo Albinsson, Jonas F. Goebel, Yi Yu, Karl Börjesson, Alexei Cravcenco, Fredrik Edhborg
Publikováno v:
Journal of the American Chemical Society
Exciton coupling between the transition dipole moments of ordered dyes in supramolecular assemblies, so-called J/H-aggregates, leads to shifted electronic transitions. This can lower the excited state energy, allowing for emission well into the near-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74043cc195a40c6e22981b9f9cc7559e
https://doi.org/10.1021/jacs.1c10654
https://doi.org/10.1021/jacs.1c10654
Autor:
Giulia Bertoli, Ángel Manu Martínez, Jonas F. Goebel, Debora Belmonte, Nardana Sivendran, Lukas J. Gooßen
Publikováno v:
Angewandte Chemie (International ed. in English).
Redox-active N-(fluoromethoxy)benzotriazoles were made accessible from fluoroacetic acid and hydroxybenzotriazoles via electrodecarboxylative coupling. After alkylation, they become effective monofluoromethoxylation reagents, enabling the photocataly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::255e75e35c2d9c482174341a2a268220
https://pubmed.ncbi.nlm.nih.gov/36385731
https://pubmed.ncbi.nlm.nih.gov/36385731
Autor:
Dominik Lichte, Nico Pirkl, Gregor Heinrich, Sayan Dutta, Jonas F. Goebel, Debasis Koley, Lukas J. Gooßen
Publikováno v:
Angewandte Chemie. 134
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::56274f36147459f3d5336e9d6b7b3a41
https://doi.org/10.1002/ange.202210009
https://doi.org/10.1002/ange.202210009
Autor:
Dominik Lichte, Nico Pirkl, Gregor Heinrich, Sayan Dutta, Jonas F. Goebel, Debasis Koley, Lukas J. Gooßen
Publikováno v:
Angewandte Chemie (International ed. in English). 61(47)
Controlling regioselectivity in C-H functionalizations is a key challenge in chemical method development. In arenes, functionalizations are most difficult to direct towards the C-H group furthest away from a substituent, in its para position. We here
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0efdcded392ef3e4c3056265ee704c3c
https://pubmed.ncbi.nlm.nih.gov/36112053
https://pubmed.ncbi.nlm.nih.gov/36112053