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Carbenes / Functional groups / Organic compounds / Persistent carbene / Indazole / Proton NMR / Nuclear magnetic resonance spectroscopy / Chemical shift / 1H / Chemistry / Nuclear magnetic resonance / Spectroscopy


Dimerisation, rhodium complex formation and rearrangements of N-heterocyclic carbenes of indazoles
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Chichester / Helsinki / Oxford / Weinheim / Stuttgart / Cambridge / /

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Fensterbank / Wiley & Sons / HP / AMD / Khartulyari A. S. / C CO / Nolan S. P. / Creative Commons / /

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Germany / United Kingdom / /

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pence / AMD / /

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Facility

Laboratory of Inorganic Chemistry / University of Hannover / University of Helsinki / 1Clausthal University of Technology / Institute of Organic Chemistry / /

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gas harmonic oscillator approximation / crude reaction product / heterocyclic transformation products / free energy difference / aforementioned ring systems / chloroform solutions / crude product / energy / metal-organic chemistry / methyl / chemical shifts / structure solution / activation energy / /

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Institute of Organic Chemistry / University of Hannover / Royal Society of Chemistry / Laboratory of Inorganic Chemistry / 1Clausthal University of Technology / Department of Chemistry / Cambridge Crystallographic Data Centre / Beilstein-Institut / University of Helsinki / /

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Tottoli (Büchi) / Gerald Dräger / Mata / Andreas Schmidt / /

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Editor / Prime Minister / rt / Corresponding author / Director / Experimental General / pm and 186.3(3) pm / /

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Maestro / C17 / Yamaha RH1 Headphone/Headset / dihedral / R1 / obtained using Maestro / /

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Inorganic Chemistry / the Beilstein Journal / /

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radiation / X-ray / Linux / ATM / pdf / crystallization / spectroscopy / Flash / /

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