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Kramer, Søren, Odabachian, Yann, Overgaard, Jacob, Rottländer, Mario, Gagosz, Fabien, Skrydstrup, Troels (2011) Taking Advantage of the Ambivalent Reactivity of Ynamides in Gold Catalysis: A Rare Case of Alkyne Dimerization. Angewandte Chemie, 123 (22). 5196-5200 doi:10.1002/ange.201100327

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Reference TypeJournal (article/letter/editorial)
TitleTaking Advantage of the Ambivalent Reactivity of Ynamides in Gold Catalysis: A Rare Case of Alkyne Dimerization
JournalAngewandte Chemie
AuthorsKramer, SørenAuthor
Odabachian, YannAuthor
Overgaard, JacobAuthor
Rottländer, MarioAuthor
Gagosz, FabienAuthor
Skrydstrup, TroelsAuthor
Year2011 (May 23)Volume123
Issue22
PublisherWiley
DOIdoi:10.1002/ange.201100327Search in ResearchGate
Generate Citation Formats
Mindat Ref. ID7316114Long-form Identifiermindat:1:5:7316114:1
GUID0
Full ReferenceKramer, Søren, Odabachian, Yann, Overgaard, Jacob, Rottländer, Mario, Gagosz, Fabien, Skrydstrup, Troels (2011) Taking Advantage of the Ambivalent Reactivity of Ynamides in Gold Catalysis: A Rare Case of Alkyne Dimerization. Angewandte Chemie, 123 (22). 5196-5200 doi:10.1002/ange.201100327
Plain TextKramer, Søren, Odabachian, Yann, Overgaard, Jacob, Rottländer, Mario, Gagosz, Fabien, Skrydstrup, Troels (2011) Taking Advantage of the Ambivalent Reactivity of Ynamides in Gold Catalysis: A Rare Case of Alkyne Dimerization. Angewandte Chemie, 123 (22). 5196-5200 doi:10.1002/ange.201100327
In(2011, May) Angewandte Chemie Vol. 123 (22) Wiley

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Kramer, Søren, Odabachian, Yann, Overgaard, Jacob, Rottländer, Mario, Gagosz, Fabien, Skrydstrup, Troels (2011) Taking Advantage of the Ambivalent Reactivity of Ynamides in Gold Catalysis: A Rare Case of Alkyne Dimerization. Angewandte Chemie International Edition, 50 (22). 5090-5094 doi:10.1002/anie.201100327
Kramer, Søren, Friis, Stig D., Xin, Zhuo, Odabachian, Yann, Skrydstrup, Troels (2011) Metal-Free Halonium Mediated Acetate Shifts of Ynamides To Access α-Halo Acrylamides/Acrylimides. Organic Letters, 13. 1750-1753 doi:10.1021/ol200269h
Xin, Zhuo, Kramer, Søren, Overgaard, Jacob, Skrydstrup, Troels (2014) Access to 1,2-Dihydroisoquinolines through Gold-Catalyzed Formal [4+2] Cycloaddition. Chemistry - A European Journal, 20 (26). 7926-7930 doi:10.1002/chem.201403290
Kramer, Søren, Skrydstrup, Troels (2012) Gold-Catalyzed Carbene Transfer to Alkynes: Access to 2,4-Disubstituted Furans. Angewandte Chemie, 124 (19). 4759-4762 doi:10.1002/ange.201200307
Gronnier, Colombe, Kramer, Søren, Odabachian, Yann, Gagosz, Fabien (2012) Cu(I)-Catalyzed Oxidative Cyclization of Alkynyl Oxiranes and Oxetanes. Journal Of The American Chemical Society, 134 (2) 828-831 doi:10.1021/ja209866a
Kramer, Søren, Skrydstrup, Troels (2012) Gold-Catalyzed Carbene Transfer to Alkynes: Access to 2,4-Disubstituted Furans. Angewandte Chemie International Edition, 51 (19). 4681-4684 doi:10.1002/anie.201200307
Kramer, Søren, Dooleweerdt, Karin, Lindhardt, Anders Thyboe, Rottländer, Mario, Skrydstrup, Troels (2009) Highly Regioselective Au(I)-Catalyzed Hydroamination of Ynamides and Propiolic Acid Derivatives with Anilines. Organic Letters, 11. 4208-4211 doi:10.1021/ol901565p
Jia, Xiuwen, Kramer, Søren, Skrydstrup, Troels, Lian, Zhong (2021) Design and Applications of a SO 2 Surrogate in Palladium‐Catalyzed Direct Aminosulfonylation between Aryl Iodides and Amines. Angewandte Chemie, 133 (13) 7429-7435 doi:10.1002/ange.202014111
Wetzel, Alexander, Gagosz, Fabien (2011) Gold-Catalyzed Transformation of 2-Alkynyl Arylazides: Efficient Access to the Valuable Pseudoindoxyl and Indolyl Frameworks. Angewandte Chemie, 123 (32). 7492-7496 doi:10.1002/ange.201102707
Andersen, Thomas L., Kramer, Søren, Overgaard, Jacob, Skrydstrup, Troels (2017) Evidence for Single-Electron Pathways in the Reaction between Palladium(II) Dialkyl Complexes and Alkyl Bromides under Thermal and Photoinduced Conditions. Organometallics, 36. 2058-2066 doi:10.1021/acs.organomet.6b00893
Muratov, Karim, Gagosz, Fabien (2022) Confinement‐Induced Selectivities in Gold(I) Catalysis—The Benefit of Using Bulky Tri‐( ortho ‐biaryl)phosphine Ligands. Angewandte Chemie, 134 (28) doi:10.1002/ange.202203452
 
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