Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Mads C. Nielsen"'
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:
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
Publikováno v:
Journal of the American Chemical Society
With the objective to increase understanding of the factors that control selectivities in high oxidation state palladium chemistry we examined the chemoselectivity in the reductive elimination of a dinuclear Pd(III) complex bearing different apical l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b5e3965c7aba6ed8620d1784e9054b2
Publikováno v:
Helvetica Chimica Acta. 95:2231-2236
(Trifluoromethyl)stannane reagents such as Bu3SnCF3 are effective in CuI-mediated trifluoromethylation reactions of aryl iodides. The reactions proceed via the intermediacy of [CuCF3] species.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::968b9213834a4d3d37e7482bf1819d7b
https://doi.org/10.1002/hlca.201200450
https://doi.org/10.1002/hlca.201200450
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
Publikováno v:
ChemInform. 44
(Trifluoromethyl)stannane reagents, such as Bu3SnCF3 (II), are found to be effective trifluoromethylation agents in CuI-mediated transformations of aryl iodides (I).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fdf6bf5771386a1b51208c21ddb78d51
https://doi.org/10.1002/chin.201317052
https://doi.org/10.1002/chin.201317052
Publikováno v:
Angewandte Chemie; Aug2006, Vol. 118 Issue 32, p5437-5441, 5p