Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Natalja Frueh"'
Publikováno v:
ChemInform. 47
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c27b3c7f11fc7ea99e105439d6dfd830
https://doi.org/10.1002/chin.201627189
https://doi.org/10.1002/chin.201627189
Autor:
Gregory Hamilton, Jeffrey Wu, Natalja Frueh, F. Dean Toste, Yi-Ming Wang, A. D. Lackner, H. P. Shunatona, Vivek Rauniyar, Robert J. Phipps, Jigar Patel, Takashi Honjo
Publikováno v:
Science. 334:1681-1684
The discovery of distinct modes of asymmetric catalysis has the potential to rapidly advance chemists' ability to build enantioenriched molecules. As an example, the use of chiral cation salts as phase-transfer catalysts for anionic reagents has enab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c280d9e058bcb0fdbff36f93f39e113
https://doi.org/10.1126/science.1213918
https://doi.org/10.1126/science.1213918
Autor:
Antonio Togni, Natalja Frueh
Publikováno v:
ChemInform. 46
The vanadium catalyzed reaction of silyl ketene imines with hypervalent iodine reagent (II) produces α-trifluoromethyl nitriles.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::457c74779829df878d0409cdd7d78ebc
https://doi.org/10.1002/chin.201512120
https://doi.org/10.1002/chin.201512120
Publikováno v:
ChemInform. 44
This is the first report of a metal-free catalytic asymmetric 1,4-fluoroamination of conjugated dienes.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c357f79e9a4c0a31666907e6b419a634
https://doi.org/10.1002/chin.201349172
https://doi.org/10.1002/chin.201349172
Publikováno v:
ChemInform. 43
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::81f560363dc330fcc6db91f760e03681
https://doi.org/10.1002/chin.201245142
https://doi.org/10.1002/chin.201245142
Autor:
Matthias S. Wiehn, Antonio Togni, Katrin Niedermann, Natalja Frueh, Aitor Moreno, Ekaterina V. Vinogradova
Publikováno v:
ChemInform. 42
Hypervalent iodine reagent (II) is used for the electrophilic trifluoromethylation of acetonitrile in the presence of azoles using catalytic amounts of N-(trifluoromethanesulfonyl)imide.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::55f119733ab49bca8df6779e8e707bfd
https://doi.org/10.1002/chin.201122042
https://doi.org/10.1002/chin.201122042