Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Karsten Donabauer"'
Autor:
Kathiravan Murugesan, Karsten Donabauer, Rok Narobe, Volker Derdau, Armin Bauer, Burkhard König
Publikováno v:
ACS Catalysis. 12:3974-3984
The selective activation of sp3 carbon–hydrogen bonds in the presence of multiple C–H bonds is challenging and remains of supreme importance in chemical research. Late-stage modification of complex molecules via sp3 C–H activation is of high pr
Publikováno v:
Angewandte Chemie
Angewandte Chemie (International Ed. in English)
Angewandte Chemie (International Ed. in English)
The metal‐free activation of C(sp3)−H bonds to value‐added products is of paramount importance in organic synthesis. We report the use of the commercially available organic dye 2,4,6‐triphenylpyrylium tetrafluoroborate (TPP) for the conversio
Autor:
Volker Derdau, Kathiravan Murugesan, Burkhard Koenig, Karsten Donabauer, Rok Narobe, Armin Bauer
The selective activation of sp3 carbon-hydrogen bonds in presence of multiple C¬-H bonds is challenging and remains of supreme importance in chemical research. Herein, we describe the activation of a C(sp3) H bond in α position to an amine via a ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d39cb524f6c6cb0beaecfdddfb29d6e
https://doi.org/10.33774/chemrxiv-2021-f7kt8
https://doi.org/10.33774/chemrxiv-2021-f7kt8
Publikováno v:
Chemical Science
We report a redox-neutral method for the generation of carbanions from benzylic C–H bonds in a photocatalytic Grignard-type reaction. The combination of photo- and hydrogen atom transfer (HAT) catalysis enables the abstraction of a benzylic hydroge
Publikováno v:
Chemistry-A European Journal, 26(57), 12945-12950. Wiley-VCH Verlag GmbH & Co. KGaA
Chemistry – A European Journal
Chemistry (Weinheim an Der Bergstrasse, Germany)
Chemistry – A European Journal
Chemistry (Weinheim an Der Bergstrasse, Germany)
A metal‐free generation of carbanion nucleophiles is of prime importance in organic synthesis. Herein we report a photocatalytic approach to the Corey–Seebach reaction. The presented method operates under mild redox‐neutral and base‐free cond
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::96e9b9fe861b905a88ecad91ba2b7967
https://research.rug.nl/en/publications/d2933270-9300-4112-b28e-2c166a3bc596
https://research.rug.nl/en/publications/d2933270-9300-4112-b28e-2c166a3bc596
We report a practical method for the alkylation of N-H bonds with alkanes using a photoinduced copper(II) peroxide catalytic system. Upon light irradiation, the peroxide serves as a hydrogen atom transfer reagent to activate stable C(sp(3))-H bonds f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee880b161487899f2e7c3ee5830ad36d
https://epub.uni-regensburg.de/43614/
https://epub.uni-regensburg.de/43614/
Autor:
Gregory S. Huff, Anna Lucia Berger, Karsten Donabauer, Stefano Crespi, Mitasree Maity, Burkhard König
Publikováno v:
Chemical Science
We present a redox-neutral method for the photocatalytic generation of carbanions. Benzylic carboxylates are photooxidized by single electron transfer; immediate CO2 extrusion and reduction of the in situ formed radical yields a carbanion capable of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::456bcf2b41dafe69e2bc5187d0d406fe
https://epub.uni-regensburg.de/40102/
https://epub.uni-regensburg.de/40102/
Publikováno v:
Chemical Science
We report a photocatalytic version of the Barbier type reaction using readily available allyl or benzyl bromides and aromatic aldehydes or ketones as starting materials to generate allylic or benzylic alcohols.
We report a photocatalytic version
We report a photocatalytic version
Autor:
Karsten Donabauer, Burkhard König
Publikováno v:
Acc. Chem. Res.
Accounts of Chemical Research
Accounts of Chemical Research
Conspectus The use of photocatalysis in organic chemistry has encountered a surge of novel transformations since the start of the 21st century. The majority of these transformations are driven by the generation and subsequent reaction of radicals, ow