Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Karl J. Bonney"'
Autor:
Ivona Jasprica, Petar Horvat, Katarina Zrnc, Karl J. Bonney, Vidar Bjornstad, Lucija Hok, Robert Vianello, Nikola Bregović, Josip Požar, Katarina Leko, Vladislav Tomišić, Ernest Meštrović
Publikováno v:
European Journal of Pharmaceutical Sciences. 187:106461
The labile β-lactam ring of penicillins and other β-lactam antibiotics is characterized by its pronounced susceptibility to various nucleophiles, acid-base reagents, oxidizing agents or even solvents like water and alcohol. However, the major pathw
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb84caf605c46c0e0607a9cbb666cbe7
https://doi.org/10.1016/j.ejps.2023.106461
https://doi.org/10.1016/j.ejps.2023.106461
Publikováno v:
Angewandte Chemie International Edition. 53:5903-5906
To date only three ligands are known to trigger the challenging reductive elimination of ArCF3 from Pd(II). We report the computational design of a bidentate trifluoromethylphosphine ligand that although exhibiting a generally ineffective small bite
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::91115e39d94a553eb4440ee75964c084
https://doi.org/10.1002/anie.201400837
https://doi.org/10.1002/anie.201400837
Publikováno v:
Angewandte Chemie. 126:6013-6016
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b966ac17b2e4d04a4a5323909ddb0eef
https://doi.org/10.1002/ange.201400837
https://doi.org/10.1002/ange.201400837
Publikováno v:
The Journal of Organic Chemistry. 78:7749-7753
The (trifluoromethyl)stannane reagent, Bu3SnCF3, was found to react under CsF activation with ketones and aldehydes to the corresponding trifluoromethylated stannane ether intermediates at room temperature in high yield. Only a mildly acidic extracti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2967a9e28b11637693d613c3b0cb3b55
https://doi.org/10.1021/jo401099e
https://doi.org/10.1021/jo401099e
Autor:
James, Clarke, Karl J, Bonney, Muhammad, Yaqoob, Savade, Solanki, Henry S, Rzepa, Andrew J P, White, David S, Millan, D Christopher, Braddock
Publikováno v:
The Journal of organic chemistry. 81(20)
The total syntheses of 12-epoxyobtusallene IV, 12-epoxyobtusallene II, obtusallene X, marilzabicycloallene C, and marilzabicycloallene D as halogenated C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::94c39b3773ff29a15163be3c8440c32d
https://pubmed.ncbi.nlm.nih.gov/27704814
https://pubmed.ncbi.nlm.nih.gov/27704814
Autor:
Karl J. Bonney, Franziska Schoenebeck
Publikováno v:
ChemInform. 45
As the accuracy of computational chemistry increases, and the advent of more powerful computers decreases the amount of time required to perform complex calculations, the use of this to investigate chemical systems becomes increasingly attractive. Pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8b84796c602d6c19d18fa33ab6d6ecc2
https://doi.org/10.1002/chin.201447268
https://doi.org/10.1002/chin.201447268
Publikováno v:
The Journal of organic chemistry. 79(24)
Building on our previous discovery and reactivity explorations of the Pd(I) dimer [(PtBu3)PdBr]2-mediated halogen exchange of aryl iodides [Chem. Sci. 2013, 4, 4434], this report presents kinetic studies of this process, giving first-order kinetic de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81410aca8dd7b419016d02b8574754c8
https://pubmed.ncbi.nlm.nih.gov/25247472
https://pubmed.ncbi.nlm.nih.gov/25247472
Publikováno v:
Angewandte Chemie (International ed. in English). 53(23)
To date only three ligands are known to trigger the challenging reductive elimination of ArCF3 from Pd(II). We report the computational design of a bidentate trifluoromethylphosphine ligand that although exhibiting a generally ineffective small bite
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::345d3f5bccc9435a70b9d23779c7de6c
https://pubmed.ncbi.nlm.nih.gov/24840791
https://pubmed.ncbi.nlm.nih.gov/24840791
Publikováno v:
ChemInform. 44
Tributyl(trifluoromethyl)stannane is successfully applied for the trifluoromethylation of a variety of carbonyl compounds.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d24f7f41696fad9522f0ad0b9473ab6d
https://doi.org/10.1002/chin.201351037
https://doi.org/10.1002/chin.201351037
Publikováno v:
The Journal of organic chemistry. 78(15)
The (trifluoromethyl)stannane reagent, Bu3SnCF3, was found to react under CsF activation with ketones and aldehydes to the corresponding trifluoromethylated stannane ether intermediates at room temperature in high yield. Only a mildly acidic extracti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::85504ab5140e430f0e2550b814530af3
https://pubmed.ncbi.nlm.nih.gov/23834264
https://pubmed.ncbi.nlm.nih.gov/23834264