Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Markus Feurer"'
Autor:
Markus Feurer, Jens Weweler, Dietmar A. Plattner, Sylwia Kacprzak, Georg Frey, Jan Streuff, Alberto Steffani, Leonardus H. Leijendekker, Daniel Kratzert
Publikováno v:
Journal of the American Chemical Society. 137:14396-14405
The titanium(III)-catalyzed cross-coupling between ketones and nitriles provides an efficient stereoselective synthesis of α-hydroxyketones. A detailed mechanistic investigation of this reaction is presented, which involves a combination of several
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bca39d8ef2c00b08bb40321e99fb0cb5
https://doi.org/10.1021/jacs.5b09223
https://doi.org/10.1021/jacs.5b09223
Publikováno v:
Angewandte Chemie. 125:7271-7274
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2f0c8f0a6a00c9aae44de2f161530e52
https://doi.org/10.1002/ange.201302460
https://doi.org/10.1002/ange.201302460
Publikováno v:
Angewandte Chemie. 124:8789-8792
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::50c7ff486b390c8c0ccb227ff8541017
https://doi.org/10.1002/ange.201204469
https://doi.org/10.1002/ange.201204469
Publikováno v:
Angewandte Chemie International Edition. 51:8661-8664
Reduction, please! The title reaction affords α-hydroxyketones, a common structural motif in biologically active natural products, in good yields and high enantioselectivities at room temperature. The commercially available ansa-titanocene 1 was fou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a77048de1c5b5a5416db5a99bd0772e
https://doi.org/10.1002/anie.201204469
https://doi.org/10.1002/anie.201204469
Publikováno v:
Chem. Commun.. 50:5370-5372
A titanium(III)-catalysed intermolecular reductive coupling of ketones or imines with nitriles is described, which gives direct access to α-hydroxylated and α-aminated ketones. This coupling reaction is cross-selective and a catalytic version of th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9dc593290829f397ad867ef04510fbce
https://doi.org/10.1039/c3cc46894a
https://doi.org/10.1039/c3cc46894a
Publikováno v:
ChemInform. 45
A Ti(III)-catalyzed intermolecular reductive coupling of ketones (I) and (IV) or imine (VI) with nitriles (II) is described, which gives direct access to α-hydroxylated and α-aminated ketones, respectively.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c87e5b5e5ad5123b4ac695eeb2105839
https://doi.org/10.1002/chin.201443042
https://doi.org/10.1002/chin.201443042
Publikováno v:
ChemInform. 44
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4b12ece3c5e16d7506b11d936b8064b9
https://doi.org/10.1002/chin.201348028
https://doi.org/10.1002/chin.201348028
Publikováno v:
Angewandte Chemie (International ed. in English). 52(28)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::11f35f3ad535fd740dff603d40ad0615
https://pubmed.ncbi.nlm.nih.gov/23740827
https://pubmed.ncbi.nlm.nih.gov/23740827
Publikováno v:
ChemInform. 44
Reduction, please! The title reaction affords α-hydroxyketones, a common structural motif in biologically active natural products, in good yields and high enantioselectivities at room temperature. The commercially available ansa-titanocene 1 was fou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::540dc4605fb9660e04bb33f2cdc885d9
https://doi.org/10.1002/chin.201305029
https://doi.org/10.1002/chin.201305029
Publikováno v:
ChemInform. 43
Highly efficient metal-free reductive coupling reactions of aldehydes and ketones with a range of nucleophiles in the presence of triflic acid as catalyst are presented.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::757540ed907e6de62d495a2405e09e14
https://doi.org/10.1002/chin.201213041
https://doi.org/10.1002/chin.201213041