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Iron-catalyzed, hydrogen-mediated reductive cyclization of 1,6-enynes and diynes: Evidence for bis(imino)pyridine ligand participation
Kevin T. Sylvester,
Paul J. Chirik
Research output
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Contribution to journal
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Article
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peer-review
185
Scopus citations
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Dive into the research topics of 'Iron-catalyzed, hydrogen-mediated reductive cyclization of 1,6-enynes and diynes: Evidence for bis(imino)pyridine ligand participation'. Together they form a unique fingerprint.
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Medicine & Life Sciences
Diynes
100%
Cyclization
74%
pyridine
64%
Hydrogen
57%
Iron
41%
Hydrogenation
41%
Iron Compounds
39%
ferrous sulfate
36%
Ligands
35%
Deuterium
34%
Atmosphere
28%
Proton Magnetic Resonance Spectroscopy
28%
Carbon
24%
Spectrum Analysis
24%
Metals
21%
Engineering & Materials Science
Cyclization
86%
Pyridine
81%
Ligands
65%
Iron
44%
Hydrogen
39%
Substrates
34%
Iron compounds
29%
Nuclear magnetic resonance spectroscopy
25%
Deuterium
23%
Dehydrogenation
23%
Precious metals
21%
Hydrogenation
20%
Labeling
16%
Catalysts
13%
Carbon
12%
Monitoring
9%
Experiments
5%
Chemical Compounds
Reductive Cyclization
66%
Enyne
63%
Pyridine
35%
Dinitrogen
29%
Turnover Frequency
27%
Dehydrogenation
22%
Deuterium(.)
22%
Ligand
21%
1H NMR Spectroscopy
20%
Cyclization Reaction
18%
Hydrogenation
18%
Catalysis
15%