Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Sebastian, Peil"'
Publikováno v:
Journal of the American Chemical Society. 144:4158-4167
Publikováno v:
Journal of the American Chemical Society. 142:18541-18553
The only recently discovered gem-hydrogenation of internal alkynes is a fundamentally new transformation, in which both H atoms of dihydrogen are transferred to the same C atom of a triple bond while the other position transforms into a discrete meta
Publikováno v:
Journal of the American Chemical Society. 144(9)
Autor:
Sebastian Peil, Alois Fürstner
Publikováno v:
Angewandte Chemie (International Ed. in English)
Enynes with a tethered carbonyl substituent are converted into substituted furan derivatives upon hydrogenation using [Cp*RuCl]4 as the catalyst. Paradoxically, this transformation can occur along two distinct pathways, each of which proceeds via dis
Autor:
Alois Fürstner, Alexandre Guthertz, Christopher P. Gordon, Tobias Biberger, Sebastian Peil, Markus Leutzsch, Christophe Copéret
Publikováno v:
Angewandte Chemie International Edition. 58:8845-8850
Parahydrogen (p-H2 ) induced polarization (PHIP) NMR spectroscopy showed that [CpX Ru] complexes with greatly different electronic properties invariably engage propargyl alcohol derivatives into gem-hydrogenation with formation of pianostool rutheniu
Publikováno v:
Angewandte Chemie International Edition. 58:8851-8856
The unusual geminal hydrogenation of a propargyl alcohol derivative with [CpX RuCl] as the catalyst entails formation of pianostool ruthenium carbenes in the first place; these reactive intermediates can be intercepted with tethered alkenes to give e
Publikováno v:
Journal of the American Chemical Society
The only recently discovered gem-hydrogenation of internal alkynes is a fundamentally new transformation, in which both H atoms of dihydrogen are transferred to the same C atom of a triple bond while the other position transforms into a discrete meta
Autor:
Dirk Trauner, Florian Küllmer, Veselin Nasufovic, Oliver Thorn-Seshold, Florian A. Gegenfurtner, Malgorzata Borowiak, Sebastian Peil, Hans-Dieter Arndt, Stefan Zahler
Publikováno v:
J Am Chem Soc
The spatiotemporally-controlled perturbation of cellular function using photopharmacology has facilitated the elucidation of biological networks and opens up new opportunities for precision medicine. Here, we introduce cell- permeable photoswitchable
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c6cb369665c451fcadd89fe4a1039ced
https://europepmc.org/articles/PMC8023282/
https://europepmc.org/articles/PMC8023282/