Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Thomas Knauber"'
Autor:
Holly E. Bonfield, Thomas Knauber, François Lévesque, Eric G. Moschetta, Flavien Susanne, Lee J. Edwards
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-4 (2020)
A pharmaceutical industry viewpoint on how the fundamental laws of photochemistry are used to identify the parameters required to implement photochemistry from lab to scale. Parameters such as photon stoichiometry and light intensity are highlighted
Externí odkaz:
https://doaj.org/article/c9016fc44960416fa1ceca7a8c7a3ae8
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 6, Iss 1, p 43 (2010)
A new protocol for the decarboxylative Heck vinylation of benzoic acids is disclosed. In the presence of a catalyst system generated in situ from Pd(OAc)2 (2 mol %), CuF2 (2 equiv), and benzoquinone (0.5 equiv) in NMP, a wide range of olefins were co
Externí odkaz:
https://doaj.org/article/7af280a9c43a4768b025fd7dbf914b92
Autor:
David F. Fernández, María González-Esguevillas, Sebastian Keess, Felix Schäfer, Jens Mohr, Andre Shavnya, Thomas Knauber, David C. Blakemore, David W. C. MacMillan
Publikováno v:
Organic Letters.
Autor:
Tiffany Q. Chen, P. Scott Pedersen, Nathan W. Dow, Remi Fayad, Cory E. Hauke, Michael C. Rosko, Evgeny O. Danilov, David C. Blakemore, Anne-Marie Dechert-Schmitt, Thomas Knauber, Felix N. Castellano, David W. C. MacMillan
Publikováno v:
J Am Chem Soc
Aryl halides are a fundamental motif in synthetic chemistry, playing a critical role in metal-mediated cross-coupling reactions and serving as important scaffolds in drug discovery. Although thermal decarboxylative functionalization of aryl carboxyli
Autor:
Nathan W. Dow, P. Scott Pedersen, Tiffany Q. Chen, David C. Blakemore, Anne-Marie Dechert-Schmitt, Thomas Knauber, David W. C. MacMillan
Publikováno v:
J Am Chem Soc
We report a copper-catalyzed strategy for arylboronic ester synthesis that exploits photoinduced ligand-to-metal charge transfer (LMCT) to convert (hetero)aryl acids into aryl radicals amenable to ambient-temperature borylation. This near-UV process
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15f291bf118e3cd39af4d59a20651dfd
https://europepmc.org/articles/PMC9676084/
https://europepmc.org/articles/PMC9676084/
Autor:
Natan J. W. Straathof, Thomas Knauber, Laura Buglioni, Véronique Gouverneur, Christopher W. am Ende, Claudio F. Meyer, Andrés A. Trabanco, Jeroen B. I. Sap, Timothy Noël, Christophe Genicot, Maurice Médebielle
Publikováno v:
Journal of the American Chemical Society
Journal of the American Chemical Society, American Chemical Society, 2020, 142 (20), pp.9181-9187. ⟨10.1021/jacs.0c03881⟩
Journal of the American Chemical Society, 142(20), 9181-9187. American Chemical Society
Journal of the American Chemical Society, American Chemical Society, 2020, 142 (20), pp.9181-9187. ⟨10.1021/jacs.0c03881⟩
Journal of the American Chemical Society, 142(20), 9181-9187. American Chemical Society
Molecular editing such as insertion, deletion, and single atom exchange in highly functionalized compounds is an aspirational goal for all chemists. Here, we disclose a photoredox protocol for the replacement of a single fluorine atom with hydrogen i
Autor:
Thomas Knauber, Remi Fayad, Michael C. Rosko, Nathan W. Dow, P. Scott Pedersen, David C. Blakemore, Evgeny O. Danilov, David W. C. MacMillan, Tiffany Chen, Anne-Marie Dechert-Schmitt, Felix N. Castellano, Cory E. Hauke
Aryl carboxylic acids are valuable, stable, and abundant functional handles in organic synthesis. Historically, their activation with established two-electron methods requires forcing conditions, and such protocols are limited in scope. In contrast,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e0b01b78569319f6e219d4aa5170a47
https://doi.org/10.26434/chemrxiv.14451117.v1
https://doi.org/10.26434/chemrxiv.14451117.v1
Autor:
Thomas Knauber, François Lévesque, Eric G. Moschetta, Lee Edwards, Holly E. Bonfield, Flavien Susanne
Publikováno v:
Nature Communications
Nature Communications, Vol 11, Iss 1, Pp 1-4 (2020)
Nature Communications, Vol 11, Iss 1, Pp 1-4 (2020)
A pharmaceutical industry viewpoint on how the fundamental laws of photochemistry are used to identify the parameters required to implement photochemistry from lab to scale. Parameters such as photon stoichiometry and light intensity are highlighted
Publikováno v:
ChemMedChem. 13:2159-2165
A new procedure for the photoredox-mediated conjugate addition of radicals that can be conveniently generated from α-amino acids to DNA-tagged Michael acceptors and styrenes is presented. This C(sp3 )-C(sp3 ) coupling tolerates a broad array of stru
Autor:
Jinshan Michael Chen, Matthew R. Reese, Christopher John Helal, Ramalakshmi Yegna Chandrasekaran, Neal W. Sach, Thomas Knauber, Joseph W. Tucker, Danica A. Rankic
Publikováno v:
Organic Letters. 19:6566-6569
A mild Ru/Ni dual catalytic desulfinative photoredox Csp2–Csp3 cross-coupling reaction of alkyl sulfinate salts with aryl halides has been developed. The optimized catalyst system, consisting of Ru(bpy)3Cl2, Ni(COD)2, and DBU, smoothly mediates the