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Journal Article

Triaryl-formazane durch C-Arylierung aus Malonsäure

MPS-Authors
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Neugebauer,  Franz A.
Department of Organic Chemistry, Max Planck Institute for Medical Research, Max Planck Society;

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Küchler,  Bernd
Max Planck Institute for Medical Research, Max Planck Society;

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http://onlinelibrary.wiley.com/doi/10.1002/jlac.19677060112/epdf
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https://doi.org/10.1002/jlac.19677060112
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Citation

Neugebauer, F. A., & Küchler, B. (1967). Triaryl-formazane durch C-Arylierung aus Malonsäure. Liebigs Annalen der Chemie, 706(1), 104-106. doi:10.1002/jlac.19677060112.


Cite as: https://hdl.handle.net/11858/00-001M-0000-002D-5030-B
Abstract
Durch Umsetzung von Malonsäure mit 3 Molen Aryldiazoniumchlorid in Dimethylformamid/Pyridin werden N.N′.C-Triaryl-formazane vom Typ 1 erhalten.