Transition‐Metal‐Free Alkylation of N‐Heterocycles with Nitriles via Heteroarylphosphonium Intermediates
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
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Online-Ressource, 5 Seiten
- Sprache
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Englisch
- Erschienen in
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In: European Journal of Organic Chemistry(27), H. 11, S.1-5 - ISSN 1434-193X
In: © 2024 Wiley‐VCH GmbH, Weinheim
- Ereignis
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Veröffentlichung
- (wo)
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Jena
- (wer)
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Friedrich-Schiller-Universität Jena
- (wann)
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2024
- Urheber
- URN
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urn:nbn:de:gbv:27-dbt-20240418-135514-008
- Rechteinformation
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 10:56 MESZ
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Beteiligte
- Schömberg, Fritz
- Perić, Milica
- Vilotijević, Ivan
- Friedrich-Schiller-Universität Jena
Entstanden
- 2024
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Synthesis of divergent N-heterocycles enabled by nitrene or gold carbene intermediates
Alpha-aminonitriles as key intermediates in the synthesis of natural products and N-heterocycles
Aziridines Cross-Dimerize to Larger N-Heterocycles
Stereoselectively fluorinated N-heterocycles: a brief survey
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Cu(OTf) 2 ‐Mediated Cross‐Coupling of Nitriles and N‐Heterocycles with Arylboronic Acids to Generate Nitrilium and Pyridinium Products **
Electrochemical access to biologically potent five-membered N-heterocycles
Photodehydrogenation of N-Heterocycles with Hexagonal Boron Carbon Nitride
Polyfunctionalizations of N-heterocycles via chemo- and regioselective metalations
Iron(II)‐Catalyzed Aerobic Biomimetic Oxidation of N‐Heterocycles
A sustainable thermochemical conversion of animal biomass to N-heterocycles
Transition‐Metal‐Free Alkylation of N‐Heterocycles with Nitriles via Heteroarylphosphonium Intermediates
Synthesis of divergent N-heterocycles enabled by nitrene or gold carbene intermediates
Alpha-aminonitriles as key intermediates in the synthesis of natural products and N-heterocycles
Aziridines Cross-Dimerize to Larger N-Heterocycles
Stereoselectively fluorinated N-heterocycles: a brief survey
Cu(OTf) 2 ‐Mediated Cross‐Coupling of Nitriles and N‐Heterocycles with Arylboronic Acids to Generate Nitrilium and Pyridinium Products **
Cu(OTf) 2 ‐Mediated Cross‐Coupling of Nitriles and N‐Heterocycles with Arylboronic Acids to Generate Nitrilium and Pyridinium Products **
Electrochemical access to biologically potent five-membered N-heterocycles
Photodehydrogenation of N-Heterocycles with Hexagonal Boron Carbon Nitride
Polyfunctionalizations of N-heterocycles via chemo- and regioselective metalations
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